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        <title>MedWorm Tags: actos</title>
        <description>MedWorm provides a medical RSS filtering service. Over 6000 RSS medical sources are combined and output via different filters. This feed contains the latest medical blog items that have been tagged with 'actos'.</description>
        <link><![CDATA[http://www.medworm.com/rss/search.php?qu=%22actos%22&t=%22actos%22&r=Exact&o=d&f=tag]]></link>
        <lastBuildDate>Sat, 03 Sep 2011 02:10:30 +0100</lastBuildDate>
        <item>
            <title>Pharmalot… Pharmalittle… Good Morning</title>
            <link>http://www.medworm.com/index.php?rid=5107899&amp;cid=t_121576_150_f&amp;fid=35777&amp;url=http%3A%2F%2Ffeedproxy.google.com%2F%7Er%2FPharmalot%2F%7E3%2FRkVSK5_Bu9Y%2F</link>
            <description>Good morning, everyone, and nice to see you again. We hope the weekend was invigorating. Now, of course, the time has come to resume the routine of meetings and deadlines, even if it is a slow time of year. To get started, yes, we are brewing that mandatory cup of stimulation, so feel free to join us. Meanwhile, here are some tidibts from around the world. Hope your day goes well and stay in touch&amp;#8230;
Pfizer And UCSD Collaborate On Early Drug Discovery (San Diego Union Tribune)
China&amp;#8217;s Healthcare Push May Curb Sales For Brand-Name Pharma (Bloomberg News)
Nestle Eyes Pfizer Formula Milk Powder Business (Business China)
EU Approves Botox For Treating Urinary Incontinence (Reuters)
Takeda Pharmaceuticals Faces Rising Number Of Actos Lawsuits (Associated Press)
Bayer Is Eyeing Pfizer ...</description>
            <author>Pharmalot</author>
            <type>blogs</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5107899</comments>
            <pubDate>Mon, 08 Aug 2011 11:50:32 +0100</pubDate>
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            <title>Another FAD Approved Diabetes Drug Found Deadly</title>
            <link>http://www.medworm.com/index.php?rid=5096658&amp;cid=t_121576_117_f&amp;fid=37824&amp;url=http%3A%2F%2Fwww.doctorkalitenko.com%2Fblog%2Fapproved-diabetes-med-deadly%2F</link>
            <description>Yet another medication, approved for years by the FDA, is now being questioned. The Food and Drug Administration is now warning that diabetes medication Actos may actually increase the risk of bladder cancer when used for over a year.

Not again! What kinds of medicines are these that are being approved when the long-term results aren’t even known. We are supposed to trust the FDA to tell us how we can make ourselves better with the least possible risk.
Germany and France have already pulled the drug , and another drug from the same family, Avandia, was pulled from US shelves earlier this year because it increased risk of heart attacks!
Though the FDA won’t pull approval for the drug, they say they will issue a warning on the label. But what does that mean for those who suffer from dia...</description>
            <author>Doctor Kalitenko antiaging blog</author>
            <type>blogs</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5096658</comments>
            <pubDate>Wed, 03 Aug 2011 16:08:58 +0100</pubDate>
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            <title>EMA Issues Cancer Warning About Actos</title>
            <link>http://www.medworm.com/index.php?rid=5051242&amp;cid=t_121576_150_f&amp;fid=35777&amp;url=http%3A%2F%2Ffeedproxy.google.com%2F%7Er%2FPharmalot%2F%7E3%2Fbj1UlOgA4Ic%2F</link>
            <description>Although France and Germany suspended use of the Actos diabetes pill, the European Medicines Agency has decided to take a more conservative approach and today recommended that Takeda Pharmaceuticals simply place new warnings about possible links to bladder cancer.
In reaching its decision, the EMA&amp;#8217;s Committee for Medicinal Products for Human Use, or CHMP, decided that there are some patients who cannot be adequately treated by other drugs and who will benefit from continued treatment with Actos. &amp;#8220;The CHMP agreed that it was not possible to further restrict the current indications of pioglitazone,&amp;#8221; according to the EMA statement.
Last week, the Agence Francaise de Securite Sanitaire des Produits de Sante (AFSSAPS) asked Takeda to withdraw Actos and based its decision by AF...</description>
            <author>Pharmalot</author>
            <type>blogs</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5051242</comments>
            <pubDate>Thu, 21 Jul 2011 17:22:47 +0100</pubDate>
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        <item>
            <title>Pharmalot… Pharmalittle… The Weekend Nears</title>
            <link>http://www.medworm.com/index.php?rid=4968909&amp;cid=t_121576_150_f&amp;fid=35777&amp;url=http%3A%2F%2Ffeedproxy.google.com%2F%7Er%2FPharmalot%2F%7E3%2FVPghfLkLLqc%2F</link>
            <description>Good morning, everyone. Another working week is about to draw to a close and already, we are daydreaming about weekend plans. Our modest agenda includes catching up on some reading, tending to the official Pharmalot grounds and spending time with our short people. And you? Now that summer is here, perhaps a drive to the beach is in order. Or curling up with a good e-book. Of course, one can always take that proverbial walk in the park. Whatever you fancy, have a great time and see you soon&amp;#8230;
Patent Overhaul Bill Clears US Senate (Reuters)
America&amp;#8217;s Vanishing Science Jobs (The New York Post)
EMA Delays Decision On Actos To July (Reuters)
FDA Inspects New Ranbaxy Plant In India (The Economic Times)
Commonly Used Drugs Raise Risk Of Death In The Elderly (Reuters)
Pfizer To Keep 350...</description>
            <author>Pharmalot</author>
            <type>blogs</type>
        <comments>http://www.medworm.com/rss/comments.php?id=4968909</comments>
            <pubDate>Fri, 24 Jun 2011 11:56:33 +0100</pubDate>
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        <item>
            <title>Pharmalot… Pharmalittle… Good Morning</title>
            <link>http://www.medworm.com/index.php?rid=4960328&amp;cid=t_121576_150_f&amp;fid=35777&amp;url=http%3A%2F%2Ffeedproxy.google.com%2F%7Er%2FPharmalot%2F%7E3%2FBKp9JbQ2S5I%2F</link>
            <description>Good morning, everyone. How are you today? Getting ready for those meetings and deadlines? We relate. There is much to do here on the Pharmalot corporate campus - reading, writing, chasing down interesting people. To prepare, we are brewing that reliable cup of stimulation - our flavor today is Rain Forest Nut. Feel free to join us. And to get things started, here are some tidbits. Have a good one and stay in touch&amp;#8230;
Bristol And Astra Diabetes Pill Faces Safety Hurdles (Bloomberg News)
Biotechs Want Faster Drug Approvals (Boston Globe)
Lilly CEO Blames Tax Laws And Immigration For Slower Innovation (Bloomberg News)
Glaxo Ordered To Give Plaintiff Lists To United Health (Legal Intelligencer)
Too Many UK Patients Are Prescribed Risky Drugs (Pharma Times)
Abbott Labs Plant Closure Delaye...</description>
            <author>Pharmalot</author>
            <type>blogs</type>
        <comments>http://www.medworm.com/rss/comments.php?id=4960328</comments>
            <pubDate>Thu, 23 Jun 2011 11:54:26 +0100</pubDate>
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        <item>
            <title>Pharmalot… Pharmalittle… The Weekend Nears</title>
            <link>http://www.medworm.com/index.php?rid=4921753&amp;cid=t_121576_150_f&amp;fid=35777&amp;url=http%3A%2F%2Ffeedproxy.google.com%2F%7Er%2FPharmalot%2F%7E3%2FPIwO-IEL5xE%2F</link>
            <description>And so another working week will soon draw to a close. This is, of course, our signal to dream about weekend doings. Our modest agenda includes spending time with Mrs. Pharmalot and the short people, catching up on our own version of R&amp;#038;D - a never-ending quest - and maybe taking a nap. And you? Perhaps there will be time for a walk in the park? A moment with someone special? Or seize the moment and make plans to enter the Republican presidential primary? Whatever you do, have a great time. See you soon&amp;#8230;
Bristol-Myers Resolves Problems At Puerto Rico Plant (Dow Jones)
Japan Does Not Plan To Recall Actos (Reuters)
Germany Joins France In Suspending Actos (Reuters)
FDA Links Some Prostate Drugs To Cancer Risk (Associated Press)
Sanofi CEO Tells Canada To Upgrade Patent Protection (...</description>
            <author>Pharmalot</author>
            <type>blogs</type>
        <comments>http://www.medworm.com/rss/comments.php?id=4921753</comments>
            <pubDate>Fri, 10 Jun 2011 12:02:18 +0100</pubDate>
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            <title>France Suspends Use Of Actos Over Cancer Risk</title>
            <link>http://www.medworm.com/index.php?rid=4921755&amp;cid=t_121576_150_f&amp;fid=35777&amp;url=http%3A%2F%2Ffeedproxy.google.com%2F%7Er%2FPharmalot%2F%7E3%2FvoFVf53PA68%2F</link>
            <description>While the FDA continues to review the Takeda Pharmaceuticals diabetes drug for bladder cancer risks, French regulators are suspending use of the pill, as well as Takeda&amp;#8217;s Competact, after reviewing pharmacovigilance data and the results of new study showed an increased risk. The meds are currently taken by about 230,000 people in France.
The decision was based on a study by a national French insurer and examined nearly 1.5 million people between 40 and 79 years old who were treated between 2006 and 2009 (read the statement). The move by the AFSSAPS will by the European Medicines Agency. Actos was approved in Europe in 2000 as an option for patients who do not benefit from metformin, a standard treatment, or metformin and insulin.
The FDA, you may recall, last fall disclosed a rewview...</description>
            <author>Pharmalot</author>
            <type>blogs</type>
        <comments>http://www.medworm.com/rss/comments.php?id=4921755</comments>
            <pubDate>Thu, 09 Jun 2011 17:06:36 +0100</pubDate>
            <guid isPermaLink="false">4921755</guid>        </item>
        <item>
            <title>Pharmalot… Pharmalittle… Good Morning</title>
            <link>http://www.medworm.com/index.php?rid=4829301&amp;cid=t_121576_150_f&amp;fid=35777&amp;url=http%3A%2F%2Ffeedproxy.google.com%2F%7Er%2FPharmalot%2F%7E3%2FlA5ZtOLK-m0%2F</link>
            <description>Good morning, everyone. A spot of rain is falling on the Pharmalot corporate campus this morning, but our spirits remain sunny. After all, as the Morning Mayor used to say: Every brand new day should be unwrapped like a precious gift. So while you tug on the ribbon, please join us for a cup of stimulation and take a moment to scan the news of the world. Hope your day goes well and you remain dry&amp;#8230;
Merck To Close Inspire HQ And Lay Off Workers (Raleigh News-Observer)
Gingrich Says Alzheimer&amp;#8217;s Research Will Save US Money (Associated Press)
Pfizer Lung Cancer Drug To Get FDA Priority Review (Reuters)
Mylan Must Pay $24M To Ipsen Over Pill Marketing (Bloomberg News)
Actos Diabetes Drug Linked To Bladder Cancer (Reuters)
Alexion To Expand Plant And Add Jobs In Rhode Island (WPRI)
Gla...</description>
            <author>Pharmalot</author>
            <type>blogs</type>
        <comments>http://www.medworm.com/rss/comments.php?id=4829301</comments>
            <pubDate>Tue, 17 May 2011 11:52:04 +0100</pubDate>
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            <title>Pharmalot… Pharmalittle… The Weekend Nears</title>
            <link>http://www.medworm.com/index.php?rid=4611004&amp;cid=t_121576_150_f&amp;fid=35777&amp;url=http%3A%2F%2Ffeedproxy.google.com%2F%7Er%2FPharmalot%2F%7E3%2F56jJMRBUxuk%2F</link>
            <description>And so, another work will soon draw to a close. This is, of course, a signal to start daydreaming about weekend plans. Our agenda is modest: spending time with our assorted short people, catching up on some reading and promenading with the official Pharmalot mascots. What about you? Getting a headstart on spring cleaning? Perhaps there is time to take a walk in the park? Or plan the rest of your lives? Whatever you do, we hope you enjoy. Meanwhile, here are some tidbits. See you soon, everyone&amp;#8230;
Pfizer Sells A Chewable Viagra Tablet In Mexico (Reuters)
FDA Rejects Lilly Drug For Alzheimer&amp;#8217;s Test (Associated Press)
Genzyme Warns EU Of Continued Thyrogen Shortage (Reuters)
New Evidence That Avandia Is Riskier Than Actos (MedPage Today)
Mylan Recalls Pills Over Labeling Mix Up (Ott...</description>
            <author>Pharmalot</author>
            <type>blogs</type>
        <comments>http://www.medworm.com/rss/comments.php?id=4611004</comments>
            <pubDate>Fri, 18 Mar 2011 11:46:59 +0100</pubDate>
            <guid isPermaLink="false">4611004</guid>        </item>
        <item>
            <title>Pharmalot… Pharmalittle… Good Morning</title>
            <link>http://www.medworm.com/index.php?rid=4512617&amp;cid=t_121576_150_f&amp;fid=35777&amp;url=http%3A%2F%2Ffeedproxy.google.com%2F%7Er%2FPharmalot%2F%7E3%2F3sAMB9LDD1o%2F</link>
            <description>Rise and shine, everyone. Another day is on the way. And as usual, we are preparing by quaffing the mandatory cup of stimulation - our flavor today is Golden French Toast. We would also like to remind your that we are hosting a webinar on requirements for disclosing payments to physicians (please look here). Meanwhile, here are a few items of interest to help you on your way. We hope today is productive and you achieve your goals. Have a good one&amp;#8230;
Texas AG Wants Actos Marketing Documents From Lilly (Dow Jones)
US Protests Canadian Drugmaker Insolvency Case (Dow Jones)
Vertex Reports Significant Data For Cystic Fibrosis Drug (The Street)
India Begins Review Of Foreign Takeovers Of Drugmakers (Economic Times)
Takeda Pulls Pain Drug That Is Now Called Useless (Japan Times)
CMO Consolida...</description>
            <author>Pharmalot</author>
            <type>blogs</type>
        <comments>http://www.medworm.com/rss/comments.php?id=4512617</comments>
            <pubDate>Wed, 23 Feb 2011 12:48:46 +0100</pubDate>
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            <title>FDA Restricts Avandia, Europe Suspends The Drug</title>
            <link>http://www.medworm.com/index.php?rid=3994339&amp;cid=t_121576_150_f&amp;fid=35777&amp;url=http%3A%2F%2Ffeedproxy.google.com%2F%7Er%2FPharmalot%2F%7E3%2FnsBOtxToxvU%2F</link>
            <description>In a move that many anticipated, the FDA is leaving the controversial Avandia diabetes pill on the market, but with restrictions for patients who are unable to control their illness by using other meds. In a statement, FDA commish says the step is an effort to &amp;#8220;strike the right balance to support clinical care.”
Want to know about the agency thinking behind this decision? You can read recommendations from several FDA officials right here.
At the same, though, the European Medicines Agency is suspending use of Avandia (here is the statement), but not revoking approval. Hamburg says there was coordination, but the FDA conducted analysis of raw data, while the EMA does not. The difference in regulatory action is based on &amp;#8220;different regulatory tools.&amp;#8221; 
GlaxoSmithKline, whic...</description>
            <author>Pharmalot</author>
            <type>blogs</type>
        <comments>http://www.medworm.com/rss/comments.php?id=3994339</comments>
            <pubDate>Thu, 23 Sep 2010 16:04:42 +0100</pubDate>
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            <title>Heart-Stopping Data For Avandia And Actos</title>
            <link>http://www.medworm.com/index.php?rid=3903131&amp;cid=t_121576_150_f&amp;fid=35777&amp;url=http%3A%2F%2Ffeedproxy.google.com%2F%7Er%2FPharmalot%2F%7E3%2FP3uVVkzjbQE%2F</link>
            <description>Just as the FDA decides the fate of the controversial Avandia diabetes pill, a new study finds the drug has the same cardiovascular risk as the rival Actos medication. In the latest analysis, about 4 percent of patients taking either pill suffered a heart attack, heart failure, both or died over a 33-month period. The study was publish in Circulation: Cardiovascular Quality and Outcomes (see abstract).
How these results may sway the FDA is unclear. Previous studies - such as this study in the Journal of the American Medical Association - have indicated that cardiovascular risk was greater with GlaxoSmithKline&amp;#8217;s Avandia than Takeda&amp;#8217;s Actos. You may recall that an FDA advisory panel last month voted to allow Avandia to remain on the market, but recommended restrictions. The agenc...</description>
            <author>Pharmalot</author>
            <type>blogs</type>
        <comments>http://www.medworm.com/rss/comments.php?id=3903131</comments>
            <pubDate>Wed, 25 Aug 2010 12:47:07 +0100</pubDate>
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            <title>Avandiagate: Glaxo And A Controversial Memo</title>
            <link>http://www.medworm.com/index.php?rid=3896091&amp;cid=t_121576_150_f&amp;fid=35777&amp;url=http%3A%2F%2Ffeedproxy.google.com%2F%7Er%2FPharmalot%2F%7E3%2FZvLxhdlArQ8%2F</link>
            <description>Avandiagate, as some have called it, appears to be never ending. In the latest twist, a letter and accompanying memo that GlaxoSmithKline wrote and distributed at the behest of the FDA is now itself the subject of a flap because some experts say the contents are misleading. And this occurs just as the agency gets set to decide the fate of the controversial Avandia diabetes pill, The New York Times writes.
The letter was supposed to bring doctors up to date on two things - the outcome of a recent FDA advisory committee meeting about Avandia, which the panel decided should remain on the market but with restrictions, and a decision by the FDA to halt Glaxo&amp;#8217;s TIDE clinical trial designed to assess cardiovascular risk when compared with the rival Actos drug (background here and here). The...</description>
            <author>Pharmalot</author>
            <type>blogs</type>
        <comments>http://www.medworm.com/rss/comments.php?id=3896091</comments>
            <pubDate>Mon, 23 Aug 2010 18:41:16 +0100</pubDate>
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            <title>As J&amp;J Suffers, Novartis Plans Triaminic Giveaway</title>
            <link>http://www.medworm.com/index.php?rid=3798817&amp;cid=t_121576_150_f&amp;fid=35777&amp;url=http%3A%2F%2Ffeedproxy.google.com%2F%7Er%2FPharmalot%2F%7E3%2F38ur4DbHE_o%2F</link>
            <description>File this under &amp;#8216;kick &amp;#8216;em when they&amp;#8217;re down.&amp;#8217; Given the problems that Johnson &amp;#038; Johnson is having with its numerous pediatric over-the-counter meds thanks to quailty control problems that shut down a key plant, one would expect rivals to step up their advertising. Novartis, however, is going further with plans to give away 250,000 bottles of Triaminic Fever Reducer Pain Reliever between Aug. 2 and 8 (look here).
“If you are going to take on children’s Tylenol, now is the time to do it,” Mick Kolassa, who heads the Medical Marketing Economics consulting firm, tells The New York Times. “It’s a beautiful opportunity. There’s concern. There’s a shortage. There’s a wide opening in the marketplace&amp;#8230;It’s saying, okay, you’ve gotten rid of the ...</description>
            <author>Pharmalot</author>
            <type>blogs</type>
        <comments>http://www.medworm.com/rss/comments.php?id=3798817</comments>
            <pubDate>Thu, 29 Jul 2010 00:07:22 +0100</pubDate>
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            <title>FDA Asks HHS To Probe Avandia Panel Member</title>
            <link>http://www.medworm.com/index.php?rid=3790923&amp;cid=t_121576_150_f&amp;fid=35777&amp;url=http%3A%2F%2Ffeedproxy.google.com%2F%7Er%2FPharmalot%2F%7E3%2F9PSZP9s4wQg%2F</link>
            <description>Remember David Capuzzi? He was a member of the recent FDA advisory committee on Avandia who, as it turns out, has also been a speaker for GlaxoSmithKline, which sells the controversial diabetes pill. The FDA, apparently, was not aware of this relationship until it was disclosed last week (see here).
Capuzzi, who is a professor of medicine and biochemistry at Thomas Jefferson University in Philadelphia was paid a total of $14,750 over the past several years, mostly for talking about Lovaza, including at least one engagement earlier this year. But there was once instance in which he spoke about Avandia, according to a Glaxo spokesman. When asked about this last week, the FDA issued a statement saying the agency &amp;#8220;takes these allegations very seriously and is investigating the matter.”...</description>
            <author>Pharmalot</author>
            <type>blogs</type>
        <comments>http://www.medworm.com/rss/comments.php?id=3790923</comments>
            <pubDate>Mon, 26 Jul 2010 12:08:13 +0100</pubDate>
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            <title>FDA Halts A Controversial Avandia Study</title>
            <link>http://www.medworm.com/index.php?rid=3776608&amp;cid=t_121576_150_f&amp;fid=35777&amp;url=http%3A%2F%2Ffeedproxy.google.com%2F%7Er%2FPharmalot%2F%7E3%2FjnP39jtGtgs%2F</link>
            <description>Less than a week after an FDA advisory panel voted to allow the controversial Avandia diabetes pill to remain on the market - but with either warnings or restrictions - the agency says new patients should not be enrolled in a long-term, randomized, controlled study known as the TIDE trial, which is designed to compare the drug with the rival Actos pill (see the FDA statement). 
The trial has been criticized for being unethical, since it compares one pill with known cardiac risks, GlaxoSmithKline&amp;#8217;s Avandia, with a seemingly safer alternative (back story here. To gain some guidance and political cover, FDA commish Margaret Hamburg recently asked an Institute of Medicine committee to explore the ethical issues the FDA faces when requiring a drugmaker to run a randomized clinical trial f...</description>
            <author>Pharmalot</author>
            <type>blogs</type>
        <comments>http://www.medworm.com/rss/comments.php?id=3776608</comments>
            <pubDate>Wed, 21 Jul 2010 17:00:30 +0100</pubDate>
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            <title>FDA Panel Members Talk About Avandia Conflicts</title>
            <link>http://www.medworm.com/index.php?rid=3776609&amp;cid=t_121576_150_f&amp;fid=35777&amp;url=http%3A%2F%2Ffeedproxy.google.com%2F%7Er%2FPharmalot%2F%7E3%2FG7wD-XKMv5o%2F</link>
            <description>Twice this week, we have learned that members of the FDA advisory panel convened to review the safety of the Avandia diabetes pill had relationships with drugmakers that had something at stake. One panelist, David Capuzzi, has an ongoing relationship with GlaxoSmithKline as a speaker, although he apparently spoke only once about the diabetes drug (see here). And Abraham Thomas has, in the past, given talks about Actos, a rival pill sold by Takeda Pharmaceuticals (see here).
The FDA is now investigating the episode surrounding Capuzzi and expects to have some decision by the end of the week. A finding that warrants further inquiry could be sent to the HHS Office of Inspector General. The agency, however, may not probe Thomas, because his speaking engagements for Takeda took place more than ...</description>
            <author>Pharmalot</author>
            <type>blogs</type>
        <comments>http://www.medworm.com/rss/comments.php?id=3776609</comments>
            <pubDate>Wed, 21 Jul 2010 16:29:54 +0100</pubDate>
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            <title>Doctor Paid By Takeda Was On FDA Avandia Panel</title>
            <link>http://www.medworm.com/index.php?rid=3772463&amp;cid=t_121576_150_f&amp;fid=35777&amp;url=http%3A%2F%2Ffeedproxy.google.com%2F%7Er%2FPharmalot%2F%7E3%2FAdAiMj9PocE%2F</link>
            <description>Another day, another conflict involving the FDA advisory panel held last week to review the Avandia diabetes pill. As it turns out, a doctor who voted against leaving Avandia on the market was a paid speaker for Takeda Pharmaceutical, which sells the rival Actos drug. The panel member is Abraham Thomas, who heads the endocrinology and diabetes division at Henry Ford Hospital in Detroit, according to The Wall Street Journal.
A Takeda spokewoman confirms that Thomas was a member of its Diabetes Speakers Bureau from September 2007 and September 2008, and gave two presentations for which he was paid between $2,000 and $3,000, but is no longer part of the program (see a recent disclosure here). &amp;#8220;I do not remember there being any issue brought up about the Takeda speakers bureau&amp;#8221; by ...</description>
            <author>Pharmalot</author>
            <type>blogs</type>
        <comments>http://www.medworm.com/rss/comments.php?id=3772463</comments>
            <pubDate>Tue, 20 Jul 2010 20:07:48 +0100</pubDate>
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        <item>
            <title>Kick ‘Em When They’re Down: New Actos Ads</title>
            <link>http://www.medworm.com/index.php?rid=3758109&amp;cid=t_121576_150_f&amp;fid=35777&amp;url=http%3A%2F%2Ffeedproxy.google.com%2F%7Er%2FPharmalot%2F%7E3%2FQxQKT1gwgt4%2F</link>
            <description>This is hardly surprising, but worth noting, nonetheless. Now that a majority of FDA advisory panel members voted in favor of allowing GlaxoSmithKline&amp;#8217;s Avandia diabetes pill to remain on the market - but with restrictions - Takeda Pharmaceuticals is taking advantage by running a national media blitz over the next two weeks in newspapers and magazines. 
The ads, which brag that &amp;#8220;Actos has been shown to lower blood sugar without increasing your risk of having a heart attack or stroke,” are appearing in 154 publications spanning 85 different markets. The national publications include The New York Times, USA Today and The Wall Street Journal, as well as such magazines as Parade, Newsweek, Time and BusinessWeek. 
Of course, the Avandia story is not over - 12 FDA panelists voted t...</description>
            <author>Pharmalot</author>
            <type>blogs</type>
        <comments>http://www.medworm.com/rss/comments.php?id=3758109</comments>
            <pubDate>Thu, 15 Jul 2010 20:45:07 +0100</pubDate>
            <guid isPermaLink="false">3758109</guid>        </item>
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            <title>Actos Launches DTC Attack on Avandia</title>
            <link>http://www.medworm.com/index.php?rid=3758104&amp;cid=t_121576_150_f&amp;fid=34889&amp;url=http%3A%2F%2Fpharmamkting.blogspot.com%2F2010%2F07%2Factos-launches-dtc-attack-on-avandia.html</link>
            <description>Ha! Takeda's sneak attack: Launches Actos DTC campaign today, a day that will live in infamy!&amp;nbsp;Read the story here. (Source: Pharma Marketing Blog)</description>
            <author>Pharma Marketing Blog</author>
            <type>blogs</type>
        <comments>http://www.medworm.com/rss/comments.php?id=3758104</comments>
            <pubDate>Thu, 15 Jul 2010 20:14:00 +0100</pubDate>
            <guid isPermaLink="false">3758104</guid>        </item>
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            <title>FDA Panel Votes To Keep Avandia On The Market</title>
            <link>http://www.medworm.com/index.php?rid=3754074&amp;cid=t_121576_150_f&amp;fid=35777&amp;url=http%3A%2F%2Ffeedproxy.google.com%2F%7Er%2FPharmalot%2F%7E3%2Fl41fGsGFSqE%2F</link>
            <description>And so the vote is in - 20 FDA advisory committee members voted for GlaxoSmithKline&amp;#8217;s Avandia diabetes pill to remain on the market, but with either restrictions or labeling changes. By comparison, 12 panel members voted to withdraw the drug. There was one abstention.
The FDA doesn&amp;#8217;t have to follow the advice of its panels, but generally does. And so, FDA officials face a Solomon-like situation - instead of maintaining the status quo or withdrawing the drug, they have impetus to develop a package of caveats that will appease some doctors and patients who maintain Avandia is their best choice, despite the cardiovascular risks. This possibility suggests Avandia could remain available elsewhere, although European regulators hold their own review next week.
For Glaxo, the outcome i...</description>
            <author>Pharmalot</author>
            <type>blogs</type>
        <comments>http://www.medworm.com/rss/comments.php?id=3754074</comments>
            <pubDate>Wed, 14 Jul 2010 20:38:05 +0100</pubDate>
            <guid isPermaLink="false">3754074</guid>        </item>
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            <title>How Should The FDA Panel Vote On Avandia?</title>
            <link>http://www.medworm.com/index.php?rid=3754076&amp;cid=t_121576_150_f&amp;fid=35777&amp;url=http%3A%2F%2Ffeedproxy.google.com%2F%7Er%2FPharmalot%2F%7E3%2Fxlpyt1HdMrc%2F</link>
            <description>After years of debate, mountains of data, harsh opinions, corporate intrigue and agency infighting, the FDA advisory committees today will vote on the fate of GlaxoSmithKline&amp;#8217;s Avandia pill. There are, of course, numerous and copious arguments for withdrawing the drug, given the evidence indicating greater cardiovascular risk and concerns over the way Glaxo handled its own data. But there is also the nagging thought that, perhaps, Actos shows a greater risk for bladder cancer.
And what about those patients for whom another treatment may not work, or work as well? Some doctors have already switched their patients (see this), and no doctor wants to keep a patient on a potentially risky medicine. But is it possible Avandia can remain available as a treatment of last resort, complete wit...</description>
            <author>Pharmalot</author>
            <type>blogs</type>
        <comments>http://www.medworm.com/rss/comments.php?id=3754076</comments>
            <pubDate>Wed, 14 Jul 2010 16:54:09 +0100</pubDate>
            <guid isPermaLink="false">3754076</guid>        </item>
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            <title>Prescription Drug Websites Need More Regulation?</title>
            <link>http://www.medworm.com/index.php?rid=3754078&amp;cid=t_121576_150_f&amp;fid=35777&amp;url=http%3A%2F%2Ffeedproxy.google.com%2F%7Er%2FPharmalot%2F%7E3%2FngseFNCG0Aw%2F</link>
            <description>That&amp;#8217;s what two professors have concluded after a preliminary study of web sites for the 100 best-selling prescription meds in 2009. Their preliminary analysis, which was presented at a recent conference in Boston, finds the sites are a &amp;#8220;bewildering and patchy mess of information&amp;#8221; that often make safety data hard to find and makes it hard to distinguish between promotion and education. 
&amp;#8220;Our analysis suggests there is a blurring of the lines which is not in anyone’s interest,&amp;#8221; Lewis Glinert, a Dartmouth University linguistics professor and one of the co-authors, tells us. &amp;#8220;“There should be a lot more regulation of these websites. The FDA should be more hands-on.&amp;#8221;
For instance, they found that about three-quarters of the sites provide as much as...</description>
            <author>Pharmalot</author>
            <type>blogs</type>
        <comments>http://www.medworm.com/rss/comments.php?id=3754078</comments>
            <pubDate>Wed, 14 Jul 2010 14:55:35 +0100</pubDate>
            <guid isPermaLink="false">3754078</guid>        </item>
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            <title>Former FDA Reviewer &amp; Avandia: In Her Own Words</title>
            <link>http://www.medworm.com/index.php?rid=3750269&amp;cid=t_121576_150_f&amp;fid=35777&amp;url=http%3A%2F%2Ffeedproxy.google.com%2F%7Er%2FPharmalot%2F%7E3%2FowzUueMZMKk%2F</link>
            <description>By now, the name Rosemary Johann-Liang may sound familiar. She is the former FDA medical reviewer who left the agency three years ago amid controversy over her work on GlaxoSmithKline’s Avandia diabetes pill (background links here). Johann-Liang had pressed for stiffer warnings on the drug, but was rebuked and excluded from safety meetings. More recenty, she was deposed as part of litigation over cardiovascular risks associated with the drug.
The deposition was not included in a letter sent by the US Senate Finance Committee to FDA commish Margaret Hamburg yesterday in which new allegations were leveled at the drugmaker for failing to disclose a study that allegedly provided greater understanding of cardiovascular risks. However, it was not released publicly and we now have the depositio...</description>
            <author>Pharmalot</author>
            <type>blogs</type>
        <comments>http://www.medworm.com/rss/comments.php?id=3750269</comments>
            <pubDate>Tue, 13 Jul 2010 17:24:10 +0100</pubDate>
            <guid isPermaLink="false">3750269</guid>        </item>
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            <title>Glaxo Hid A Study On Avandia Risks For A Decade</title>
            <link>http://www.medworm.com/index.php?rid=3750273&amp;cid=t_121576_150_f&amp;fid=35777&amp;url=http%3A%2F%2Ffeedproxy.google.com%2F%7Er%2FPharmalot%2F%7E3%2FA9oLchiBF7k%2F</link>
            <description>Nothing like dropping a bombshell on the morning of a crucial FDA advisory committee meeting. But GlaxoSmithKline quietly began a study in 1999 to determine if the cardiovascular risks of its Avandia diabetes pill were greater than with Actos, a similar drug, and instead of publishing the results, the drugmaker spent 11 years trying to cover them up, according to The New York Times.
The results were never provided to the FDA or posted on the Glaxo web site, the paper continues, citing these documents - please see Attachments A and E. &amp;#8220;This was done for the US business, way under the radar,” Martin Freed, a SmithKline exec, wrote in a March 29, 2001, e-mail about the results. “Per Sr. Mgmt request, these data should not see the light of day to anyone outside of GSK.” The study w...</description>
            <author>Pharmalot</author>
            <type>blogs</type>
        <comments>http://www.medworm.com/rss/comments.php?id=3750273</comments>
            <pubDate>Tue, 13 Jul 2010 12:30:43 +0100</pubDate>
            <guid isPermaLink="false">3750273</guid>        </item>
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            <title>FDA, Avandia &amp; High Stakes: Dan Carpenter Explains</title>
            <link>http://www.medworm.com/index.php?rid=3746986&amp;cid=t_121576_150_f&amp;fid=35777&amp;url=http%3A%2F%2Ffeedproxy.google.com%2F%7Er%2FPharmalot%2F%7E3%2F-CbIiY0mVwQ%2F</link>
            <description>This report could change the Avandia game entirely. For one, if Marciniak’s view is widely held at the FDA (or it’s widely shared among its advisory committee), then we no longer have a case in which the clinical trials point one way and the observational evidence points the other way. More important, because Marciniak is a CDER reviewer, we no longer have a case in which the FDA’s ‘trialists’ are entirely at odds with its ‘observationalists.’ In other words, Marciniak’s memo may create doubt among many CDER medical reviewers who favor randomized clinical trials but who may come to doubt GSK’s credibility in running them. That kind of loss of trust can be severely destructive for a company. As far as I can tell, Marciniak’s voice is a new one in this debate, and combine...</description>
            <author>Pharmalot</author>
            <type>blogs</type>
        <comments>http://www.medworm.com/rss/comments.php?id=3746986</comments>
            <pubDate>Mon, 12 Jul 2010 13:09:05 +0100</pubDate>
            <guid isPermaLink="false">3746986</guid>        </item>
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            <title>Levin On Avandia: ‘Since 07, We Lost Some People’</title>
            <link>http://www.medworm.com/index.php?rid=3746988&amp;cid=t_121576_150_f&amp;fid=35777&amp;url=http%3A%2F%2Ffeedproxy.google.com%2F%7Er%2FPharmalot%2F%7E3%2FAWU1I2vktoM%2F</link>
            <description>Three years ago, an FDA advisory committee voted 22-to-1 to permit GlaxoSmithKline&amp;#8217;s Avandia diabetes pill to remain on the market. The move came shortly after a new meta-analysis found an increased risk of heart attacks and strokes associated with the drug. A similar scenario is unfolding this week as the FDA convenes another meeting to explore the same issue. We spoke with Arthur Levin, who heads the Center for Medical Consumers and was the lone vote in 2007 in favor of withdrawing Avania&amp;#8230;
Pharmalot: It&amp;#8217;s been three years since you voted in favor of withdrawing Avandia? Is this deja vu? Has anything really changed?
Levin: Well, a lot of time has gone by and what has changed is that we have a lot more evidence that this risk is real. It&amp;#8217;s not like the alarm bells t...</description>
            <author>Pharmalot</author>
            <type>blogs</type>
        <comments>http://www.medworm.com/rss/comments.php?id=3746988</comments>
            <pubDate>Mon, 12 Jul 2010 12:39:20 +0100</pubDate>
            <guid isPermaLink="false">3746988</guid>        </item>
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            <title>Avandia, Heart Attacks &amp; An Upcoming FDA Meeting</title>
            <link>http://www.medworm.com/index.php?rid=3706994&amp;cid=t_121576_150_f&amp;fid=35777&amp;url=http%3A%2F%2Ffeedproxy.google.com%2F%7Er%2FPharmalot%2F%7E3%2FennOAQ5bM08%2F</link>
            <description>Just three weeks before what is certain to be a tense FDA advisory committee meeting, the study showing the Avandia diabetes pill increases the the risk of stroke, heart failure and death compared with Takeda Pharmaceutical&amp;#8217;s Actos has been peer-reviewed and published (see this). This is the same paper that was leaked to us earlier this month (see here) and now appears online at the Journal of the American Medical Association web site. 
The study, which evaluated data from 227,571 Medicare patients between 2006 and 2009 with an average of 74.4 years, found there 1,746 heart attacks, of which 21.7 percent fatal; 1,052 strokes and 7.3 percent fatal; 3,307 hospitalizations for heart failure, including 2.6 percent that were fatal; and 2,562 deaths for all causes. Although the analysis sh...</description>
            <author>Pharmalot</author>
            <type>blogs</type>
        <comments>http://www.medworm.com/rss/comments.php?id=3706994</comments>
            <pubDate>Mon, 28 Jun 2010 14:18:07 +0100</pubDate>
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            <title>On The Couch… Weekend Reading</title>
            <link>http://www.medworm.com/index.php?rid=3679914&amp;cid=t_121576_150_f&amp;fid=35777&amp;url=http%3A%2F%2Ffeedproxy.google.com%2F%7Er%2FPharmalot%2F%7E3%2FMXgDoWb_u_s%2F</link>
            <description>A sunny day here on the Pharmalot corporate campus, where we are using some spare moments to catch up on our reading. And of course, we are leisurely quaffing a few cups of stimulation. Later, we plan to grab a bite with Mrs. Pharmalot and The Pharmalittles in honor of you-know-what day. Whatever your plans, we hope the day is enjoyable. Meanwhile, here are a few stray items to keep you fresh. And remember to say hi to your dad. Have a great time…
Patents on blockbusters are expiring. The human genome is not delivering. And the low-hanging fruit was long ago picked from the orchard of obvious follow-ups. Adrian Ivinson, director of Harvard&amp;#8217;s NeuroDiscovery Center, is reminded of the shifts underway in the industry every time he looks out of his Cambridge, Ma., window at the &amp;#8220;...</description>
            <author>Pharmalot</author>
            <type>blogs</type>
        <comments>http://www.medworm.com/rss/comments.php?id=3679914</comments>
            <pubDate>Sun, 20 Jun 2010 14:13:01 +0100</pubDate>
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            <title>Is The FDA Suppressing An Avandia Study?</title>
            <link>http://www.medworm.com/index.php?rid=3648798&amp;cid=t_121576_150_f&amp;fid=35777&amp;url=http%3A%2F%2Ffeedproxy.google.com%2F%7Er%2FPharmalot%2F%7E3%2FIMny61PkBdU%2F</link>
            <description>A new observational study comparing the controversial Avandia diabetes pill found an increased risk of various cardiovascular problems compared with Actos, a similar drug but one that hasn&amp;#8217;t raised as many concerns. Yet one co-author, FDA reviewer David Graham, recently wrote top FDA officials over concerns that agency supervisors hadn&amp;#8217;t given clearance for the study to be submitted for publication. (You can see Graham&amp;#8217;s email to FDA commish Margaret Hamburg further down).
The May 28 draft manuscript indicates the authors reviewed records of 227,571 Medicare patients with an average age of 74.4 years who were followed for up to three years after starting either of the two pills. The results - GlaxoSmithKline&amp;#8217;s Avandia increased the risk of stroke by 27 percent; hear...</description>
            <author>Pharmalot</author>
            <type>blogs</type>
        <comments>http://www.medworm.com/rss/comments.php?id=3648798</comments>
            <pubDate>Thu, 10 Jun 2010 16:07:11 +0100</pubDate>
            <guid isPermaLink="false">3648798</guid>        </item>
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            <title>The FDA Denies Suppressing An Avandia Study</title>
            <link>http://www.medworm.com/index.php?rid=3652693&amp;cid=t_121576_150_f&amp;fid=35777&amp;url=http%3A%2F%2Ffeedproxy.google.com%2F%7Er%2FPharmalot%2F%7E3%2FIMny61PkBdU%2F</link>
            <description>A new observational study comparing the controversial Avandia diabetes pill found an increased risk of various cardiovascular problems compared with Actos, a similar drug but one that hasn&amp;#8217;t raised as many concerns. Yet one co-author, FDA reviewer David Graham, recently wrote top FDA officials over concerns that agency supervisors hadn&amp;#8217;t given clearance for the study to be submitted for publication. (You can see Graham&amp;#8217;s email to FDA commish Margaret Hamburg further down).
The May 28 manuscript indicates the authors reviewed records of 227,571 Medicare patients with an average age of 74.4 years who were followed for up to three years after starting either of the two pills. The results - GlaxoSmithKline&amp;#8217;s Avandia increased the risk of stroke by 27 percent; heart fail...</description>
            <author>Pharmalot</author>
            <type>blogs</type>
        <comments>http://www.medworm.com/rss/comments.php?id=3652693</comments>
            <pubDate>Thu, 10 Jun 2010 15:33:43 +0100</pubDate>
            <guid isPermaLink="false">3652693</guid>        </item>
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            <title>Bioethics Expert To FDA: Scrap Glaxo’s Avandia Trial</title>
            <link>http://www.medworm.com/index.php?rid=3603868&amp;cid=t_121576_150_f&amp;fid=35777&amp;url=http%3A%2F%2Ffeedproxy.google.com%2F%7Er%2FPharmalot%2F%7E3%2FM_qutDlC97A%2F</link>
            <description>The hoopla continues over the TIDE trial, which GlaxoSmithKline hopes will vindicate its Avandia diabetes pill. You may recall that Avandia was tied in earlier studies to an increased risk of heart attacks and the TIDE trial compares Avandia with Takeda Pharmaceuticals&amp;#8217; Actos, which hasn&amp;#8217;t generated the same degree of safety concerns.
However, the trial has been criticized for being unethical, since it compares one pill with known cardiac risks with a seemingly safer alternative. The FDA, in fact, may halt the trial prior to a July 13 advisory committee meeting to review Avandia (see here) and, meanwhile, Glaxo is having trouble enrolling patients (see here). And now another heavy hitter has joined the chorus of concerns and is demanding the agency end the trial.
Ruth Macklin, ...</description>
            <author>Pharmalot</author>
            <type>blogs</type>
        <comments>http://www.medworm.com/rss/comments.php?id=3603868</comments>
            <pubDate>Thu, 27 May 2010 16:06:47 +0100</pubDate>
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            <title>Glaxo Struggles To Recruit Patients For Avandia Trial</title>
            <link>http://www.medworm.com/index.php?rid=3581838&amp;cid=t_121576_150_f&amp;fid=35777&amp;url=http%3A%2F%2Ffeedproxy.google.com%2F%7Er%2FPharmalot%2F%7E3%2F7jADiryRMOk%2F</link>
            <description>The big drugmaker is having difficulty recruiting patients for the TIDE trial, which compares the Avandia diabetes pill with Takeda Pharmaceutical’s Actos, but there are ongoing concerns that the study is unethical because it tests a drug with known cardiac risks with what appears to be a safer alternative. And now investigative sites have withdrawn due to poor enrollment, The Wall Street Journal reports.
One site, Wake Forest University Baptist Medical Center in North Carolina, is &amp;#8220;not succeeding in recruiting anybody,&amp;#8221; although efforts to enlist patients began last year, William Applegate, dean of Wake Forest&amp;#8217;s medical school, tells the paper. The FDA, meanwhile, is considering putting an end to the trial (see here) and some physicians agree it should be ended (look h...</description>
            <author>Pharmalot</author>
            <type>blogs</type>
        <comments>http://www.medworm.com/rss/comments.php?id=3581838</comments>
            <pubDate>Thu, 20 May 2010 12:29:07 +0100</pubDate>
            <guid isPermaLink="false">3581838</guid>        </item>
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            <title>Takeda Pharma To Cut More Than 1,400 US Jobs</title>
            <link>http://www.medworm.com/index.php?rid=3556372&amp;cid=t_121576_150_f&amp;fid=35777&amp;url=http%3A%2F%2Ffeedproxy.google.com%2F%7Er%2FPharmalot%2F%7E3%2FSyPtQtSWdQ4%2F</link>
            <description>Japan&amp;#8217;s largest drug maker, which employs about 5,000 people in the US, is cutting back as part of a restructuring in response to declining sales and looming generic competition for its Actos diabetes drug in two years. About 28 percent of the 1,300 employees who work US headquarters in Deerfield, Illinois, will be eliminated, according to The Chicago Tribune. And 20 percent of the 840 positions at the Global Research and Development Center are also going. 
&amp;#8220;The business environment for the pharmaceutical industry is changing dramatically, with the pharmaceutical industry as a whole facing barriers to technological innovation that have halted progress in breakthrough novels drugs, stricter approval processes for new drugs in advanced nations, and radical upheaval in healthcare ...</description>
            <author>Pharmalot</author>
            <type>blogs</type>
        <comments>http://www.medworm.com/rss/comments.php?id=3556372</comments>
            <pubDate>Wed, 12 May 2010 13:43:04 +0100</pubDate>
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            <title>Avandia: One Drug, But So Many Opinions</title>
            <link>http://www.medworm.com/index.php?rid=3515635&amp;cid=t_121576_150_f&amp;fid=35777&amp;url=http%3A%2F%2Ffeedproxy.google.com%2F%7Er%2FPharmalot%2F%7E3%2FjIXtyqL7RSU%2F</link>
            <description>Yesterday, the House Agriculture FDA Appropriations Subcommittee held a hearing on drug safety with a special emphasis on Avandia, the GlaxoSmithKline diabetes pill that has been linked to heart problems amid controversy over the extent to which the drugmaker disclosed the risks. The hearing comes two months after the Senate Finance Committee released a report detailing internal disagreement within the FDA and new revelations about Glaxo deliberations. Meanwhile, the FDA plans an advisory committee meeting in July, but may halt a 16,000-patient safety study called TIDE over ethics concerns (background). Here&amp;#8217;s what a few of those speaking had to say&amp;#8230;.
Rosa DeLauro, subscommittee chair: When this drug was approved in 1999, the FDA requested the Glaxo conduct a post-market study,...</description>
            <author>Pharmalot</author>
            <type>blogs</type>
        <comments>http://www.medworm.com/rss/comments.php?id=3515635</comments>
            <pubDate>Thu, 29 Apr 2010 12:52:32 +0100</pubDate>
            <guid isPermaLink="false">3515635</guid>        </item>
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            <title>That Crucial Avandia Trial Raises More Concerns</title>
            <link>http://www.medworm.com/index.php?rid=3508447&amp;cid=t_121576_150_f&amp;fid=35777&amp;url=http%3A%2F%2Ffeedproxy.google.com%2F%7Er%2FPharmalot%2F%7E3%2FcHEwkbD7WIg%2F</link>
            <description>Is the TIDE trial going to get derailed? The FDA is already considering whether the studyl, which compares GlaxoSmithKline&amp;#8217;s Avandia with Takeda Pharmaceutical&amp;#8217;s Actos, should continue over concerns that it may be unethical to compare a drug with known cardiac risks with what appears to be a safer alternative (see here). The deliberations occur in the run-up to an FDA advisory committee meeting in July to review Avandia and cardiac risks.
Now, some physicians are telling heartwire that the trial, which is supposed to involve thousands of patients, should be stopped, in part because informed consent forms may not reflect the most up-to-date Avandia safety info, an issue that FDA commish Margaret Hamburg alluded to in a recent letter to US Senator Chuck Grassley, who is investiga...</description>
            <author>Pharmalot</author>
            <type>blogs</type>
        <comments>http://www.medworm.com/rss/comments.php?id=3508447</comments>
            <pubDate>Tue, 27 Apr 2010 12:43:50 +0100</pubDate>
            <guid isPermaLink="false">3508447</guid>        </item>
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            <title>The FDA May Halt The Avandia Safety Study</title>
            <link>http://www.medworm.com/index.php?rid=3483117&amp;cid=t_121576_150_f&amp;fid=35777&amp;url=http%3A%2F%2Ffeedproxy.google.com%2F%7Er%2FPharmalot%2F%7E3%2F8YlODPoiDBY%2F</link>
            <description>The FDA may halt a safety study involving patients taking GlaxoSmithKline&amp;#8217;s Avandia diabetes pill, which could also determine whether the drug stays on the market, The Wall Street Journal reports. You may recall recent studies tied the med to an increased risk of heart attacks, and in 2007, the FDA approved a trial comparing Avandia with Takeda Pharmaceutical&amp;#8217;s Actos, which hasn&amp;#8217;t generated the same degree of safety concerns.
But some scientists say it is unethical to compare a drug with known cardiac risks with a seemingly safer alternative, and that Avandia should be pulled from the market. For several years, the FDA pooh-poohed these concerns, but has now called in the Institute of Medicine to review the ethics of head-to-head studies, according to the Journal.
In a le...</description>
            <author>Pharmalot</author>
            <type>blogs</type>
        <comments>http://www.medworm.com/rss/comments.php?id=3483117</comments>
            <pubDate>Mon, 19 Apr 2010 12:35:24 +0100</pubDate>
            <guid isPermaLink="false">3483117</guid>        </item>
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            <title>Most Avandia Supporters Have Ties To Glaxo</title>
            <link>http://www.medworm.com/index.php?rid=3383081&amp;cid=t_121576_150_f&amp;fid=35777&amp;url=http%3A%2F%2Ffeedproxy.google.com%2F%7Er%2FPharmalot%2F%7E3%2FCvh0VnrwATI%2F</link>
            <description>And so the debate over untoward conflicts of interest rages on. The latest installment is brought to you by BMJ, which has published a paper by a team of Mayo Clinic Researchers, who found most scientists who published articles supporting GlaxoSmithKline&amp;#8217;s Avandia diabetes pill after it was linked to a risk of heart attacks in 2007 had financial ties to the drugmaker.
Of 202 articles reviewed, 108 - or 53 percent - had a conflict of interest statement, and 90 authors, or 45 percent, had financial conflicts of interest. Authors with a favorable view of the risk of heart attack were more likely to have financial conflicts of interest with makers of antihyperglycaemic drugs, in general, and with drugmakers who sell Avandia and similar pills - Eli Lilly and Takeda - than authors who had ...</description>
            <author>Pharmalot</author>
            <type>blogs</type>
        <comments>http://www.medworm.com/rss/comments.php?id=3383081</comments>
            <pubDate>Fri, 19 Mar 2010 12:05:06 +0100</pubDate>
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        <item>
            <title>Avandia, Heart Attacks &amp; An Internal FDA Battle</title>
            <link>http://www.medworm.com/index.php?rid=3290991&amp;cid=t_121576_150_f&amp;fid=35777&amp;url=http%3A%2F%2Ffeedproxy.google.com%2F%7Er%2FPharmalot%2F%7E3%2FzmPNNoYg-CQ%2F</link>
            <description>Avandia is needlessly causing hundreds of cases of heart attacks and heart failure each month, according to confidential government reports, The New York Times writes. Moreover, if every diabetic taking Avandia were given Actos instead, about 500 heart attacks and 300 cases of heart failure would be avoided each month. The pill was linked to 304 deaths during the third quarter of 2009, and a report by the FDA&amp;#8217;s David Graham and Kate Gelperin concludes the pill should be yanked (Graham said this in 2007 - look).
Some FDA officials want Avandia withdrawn because they believe a safer alternative exists, the Times adds, noting others insist studies offer contradictory info and Avandia should remain an option. GlaxoSmithKline, which makes the pill, says it studied Avandia extensively and ...</description>
            <author>Pharmalot</author>
            <type>blogs</type>
        <comments>http://www.medworm.com/rss/comments.php?id=3290991</comments>
            <pubDate>Sat, 20 Feb 2010 15:29:18 +0100</pubDate>
            <guid isPermaLink="false">3290991</guid>        </item>
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            <title>GSK - Avandia: “Rosiglitazone should be removed from the market,”</title>
            <link>http://www.medworm.com/index.php?rid=3290989&amp;cid=t_121576_150_f&amp;fid=34768&amp;url=http%3A%2F%2Fpharmagossip.blogspot.com%2F2010%2F02%2Fgsk-avandia-rosiglitazone-should-be.html</link>
            <description>Hundreds of people taking Avandia, a controversial diabetes medicine, needlessly suffer heart attacks and heart failure each month, according to confidential government reports that recommend the drug be removed from the market.The reports, obtained by The New York Times, say that if every diabetic now taking Avandia were instead given a similar pill named Actos, about 500 heart attacks and 300 cases of heart failure would be averted every month because Avandia can hurt the heart. Avandia, intended to treat Type 2 diabetes, is known as rosiglitazone and was linked to 304 deaths during the third quarter of 2009.More from Gardiner Harris at the NYT (Source: PharmaGossip)</description>
            <author>PharmaGossip</author>
            <type>blogs</type>
        <comments>http://www.medworm.com/rss/comments.php?id=3290989</comments>
            <pubDate>Sat, 20 Feb 2010 04:55:00 +0100</pubDate>
            <guid isPermaLink="false">3290989</guid>        </item>
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            <title>The Truth About Afresa Inhalable Insulin: A Chat with Al Mann</title>
            <link>http://www.medworm.com/index.php?rid=2999749&amp;cid=t_121576_134_f&amp;fid=34841&amp;url=http%3A%2F%2Fwww.diabetesmine.com%2F2009%2F11%2Fthe-truth-about-afresa-inhalable-insulin-a-chat-with-al-mann.html</link>
            <description>Al Mann, CEO of MannKind Corp., is something of a legend in his own time.  He not only founded MiniMed, acquired by Medtronic, but also four other successful medical companies. He&amp;#8217;s a billionaire, with his own Biomedical Engineering Institute at the University of Southern California (USC), so we can assume that he&amp;#8217;s not just championing [...] (Source: Diabetes Mine)</description>
            <author>Diabetes Mine</author>
            <type>blogs</type>
        <comments>http://www.medworm.com/rss/comments.php?id=2999749</comments>
            <pubDate>Tue, 17 Nov 2009 16:02:31 +0100</pubDate>
            <guid isPermaLink="false">2999749</guid>        </item>
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            <title>Avandia, Diabetes Drug, May Cause Problems</title>
            <link>http://www.medworm.com/index.php?rid=2716033&amp;cid=t_121576_111_f&amp;fid=36048&amp;url=http%3A%2F%2Ffeeds.b5media.com%2F%7Er%2Fb5media%2FAHeartyLife%2F%7E3%2FD6BYhuhwrLU%2F</link>
            <description>Avandia (rosiglitazone), a medication for people with type 2 diabetes, has been the subject of studies evaluating its safety and the results aren&amp;#8217;t what Glaxo (the manufacturer) had hoped for. According to researchers in Toronto, Canada, elderly people who take Avandia may have an increased risk of heart failure and death.
The researchers didn&amp;#8217;t, however, find the same results that American researchers found two years earlier, which suggested that Avandia also increased the risk of heart attacks. The Canadian researchers found no difference between patients who took Avandia and another type of medication, Actos (pioglitazone), and the rate of heart attacks among them
The researchers studied 40,000 patients over the age of 65 who took Avandia or Actos. For every 93 patients, the...</description>
            <author>A Hearty Life</author>
            <type>blogs</type>
        <comments>http://www.medworm.com/rss/comments.php?id=2716033</comments>
            <pubDate>Wed, 19 Aug 2009 12:54:58 +0100</pubDate>
            <guid isPermaLink="false">2716033</guid>        </item>
        <item>
            <title>News You Missed: Actos Strongly Linked to Retinopathy</title>
            <link>http://www.medworm.com/index.php?rid=2376618&amp;cid=t_121576_134_f&amp;fid=35137&amp;url=http%3A%2F%2Fdiabetesupdate.blogspot.com%2F2009%2F04%2Fnews-you-missed-actos-strongly-linked.html</link>
            <description>This study was published in an Ophthalmology journal, rather than a diabetes journal, and seems to have been completely ignored by the diabetes press. Here's the study:Glitazone Use Associated with Diabetic Macular Edema Donald S. Fong. Am J Ophth Volume 147, Issue 4, Pages 583-586.e1 (April 2009)This study analyzed the records of 170,000 people with diabetes treated by Kaiser Permanente Southern California. The researchers found that In 2006, there were 996 new cases of ME. Glitazone users were more likely to develop ME in 2006 (odds ratio [OR], 2.6; 95% confidence interval [CI], 2.4 to 3.0). After excluding patients who did not have the drug benefit, did not have an eye exam, and had a HgA1c (Source: Diabetes Update)</description>
            <author>Diabetes Update</author>
            <type>blogs</type>
        <comments>http://www.medworm.com/rss/comments.php?id=2376618</comments>
            <pubDate>Wed, 29 Apr 2009 16:05:00 +0100</pubDate>
            <guid isPermaLink="false">2376618</guid>        </item>
        <item>
            <title>Avandia, Actos And Bone Fractures In Women</title>
            <link>http://www.medworm.com/index.php?rid=2033599&amp;cid=t_121576_150_f&amp;fid=35777&amp;url=http%3A%2F%2Ffeeds.feedburner.com%2F%7Er%2FPharmalot%2F%7E3%2F481603244%2F</link>
            <description>The long-term use of the so-called glitizones, a popular class of diabetes pills that includes Glaxo&amp;#8217;s Avandia and Takeda&amp;#8217;s Actos, drugs doubles the risk of bone fractures in women with type 2 diabetes, according to a study in the Canadian Medical Association Journal.
The study reviewed 10 previous clinical trials, and for every 20 women in their 70s with type 2 diabetes who took the drugs for at least one year, one has a chance of suffering a fracture. In women in their mid-50s, the figure equals one fracture in every 55 women. That&amp;#8217;s more than double the normal risk for those age groups.
An accompanying editorial concludes that &amp;#8220;the ongoing accumulation of evidence of harm for (this class of drugs) is unsettling to clinicians and patients and threatens to undermin...</description>
            <author>Pharmalot</author>
            <type>blogs</type>
        <comments>http://www.medworm.com/rss/comments.php?id=2033599</comments>
            <pubDate>Thu, 11 Dec 2008 12:10:58 +0100</pubDate>
            <guid isPermaLink="false">2033599</guid>        </item>
        <item>
            <title>New Study Spins Actos' Health Risk While Ignoring Its True Dangers</title>
            <link>http://www.medworm.com/index.php?rid=2005939&amp;cid=t_121576_134_f&amp;fid=35137&amp;url=http%3A%2F%2Fdiabetesupdate.blogspot.com%2F2008%2F12%2Fnew-study-spins-actos-health-risk-but.html</link>
            <description>The bad news about Avandia's association with heart attack has been good news for Takeda, the maker of Actos. Both drugs are thiazolidinediones (TZD). They help lower blood sugar by reducing insulin resistance. Until the ACCORD study results came out last year, Avandia was prescribed far more frequently than Actos. Now, with Avandia's reputation in tatters, Takeda has been pushing doctors to switch their Type 2 patients to Actos.The latest effort in this direction was the publication of a new study that is being spun in the media as showing the Actos is far safer than Avandia. Here's a link to the actual study: Comparison of Cardiovascular Outcomes in Elderly Patients With Diabetes Who Initiated Rosiglitazone vs Pioglitazone Therapy. Wolfgang C. Winkelmayer, MD, ScD; Soko Setoguchi, MD, Dr...</description>
            <author>Diabetes Update</author>
            <type>blogs</type>
        <comments>http://www.medworm.com/rss/comments.php?id=2005939</comments>
            <pubDate>Mon, 01 Dec 2008 20:34:00 +0100</pubDate>
            <guid isPermaLink="false">2005939</guid>        </item>
        <item>
            <title>The glitazone wars - this just in</title>
            <link>http://www.medworm.com/index.php?rid=1990761&amp;cid=t_121576_150_f&amp;fid=34768&amp;url=http%3A%2F%2Fpharmagossip.blogspot.com%2F2008%2F11%2Fglitazone-wars-this-just-in.html</link>
            <description>&quot;Those who started with rosiglitazone had a 15 percent increased risk of dying from any cause compared with pioglitazone.&quot; Reuters (Source: PharmaGossip)</description>
            <author>PharmaGossip</author>
            <type>blogs</type>
        <comments>http://www.medworm.com/rss/comments.php?id=1990761</comments>
            <pubDate>Tue, 25 Nov 2008 12:01:00 +0100</pubDate>
            <guid isPermaLink="false">1990761</guid>        </item>
        <item>
            <title>Pharmalot… Pharmalittle… G’Morning, Everyone</title>
            <link>http://www.medworm.com/index.php?rid=1991567&amp;cid=t_121576_150_f&amp;fid=35777&amp;url=http%3A%2F%2Ffeeds.feedburner.com%2F%7Er%2FPharmalot%2F%7E3%2F464959599%2F</link>
            <description>A bit dreary here in the nation&amp;#8217;s medicine chest as we awake to gray skies and a slight drizzle. Still, our spirits are high. And despite the looming holiday here in the US, there is much to do. So time to get started. Here are a few items to help you along. Hope your day is meaningful&amp;#8230;
AstraZeneca, Abraxis To End Cancer Drug Trial (Reuters)
Lilly Outsources Clinical-Data Management (PharmaTimes)
Roche Agrees To Pay $50M For Memory Pharma (The Star-Ledger)
Crestor Scrips Rise After Jupiter Study (Reuters)
Schering-Plough Sees 5 NDAs In 2009 (Dow Jones)
FDA Panel OKs New Gout Drug (WebMD)
Avandia Riskier Than Actos For Older Diabetics (Philly.com) (Source: Pharmalot)</description>
            <author>Pharmalot</author>
            <type>blogs</type>
        <comments>http://www.medworm.com/rss/comments.php?id=1991567</comments>
            <pubDate>Tue, 25 Nov 2008 11:48:34 +0100</pubDate>
            <guid isPermaLink="false">1991567</guid>        </item>
        <item>
            <title>Are Costly Diabetes Pills Doing Any Good?</title>
            <link>http://www.medworm.com/index.php?rid=1969317&amp;cid=t_121576_150_f&amp;fid=35777&amp;url=http%3A%2F%2Ffeeds.feedburner.com%2F%7Er%2FPharmalot%2F%7E3%2F457574314%2F</link>
            <description>An increasing number of type 2 diabetes patients in the US are being treated by an increasingly complex mix of therapies, according to a study in the Archives of Internal Medicine, which questions whether the meds are actually going to improve outcomes.
Between 1994 and 2007, the estimated number of yearly patient visits to treat diabetes increased from 25 million to 36 million. During the period reviewed by the study, the number of doctor visits in which only one drug was prescribed decreased from 82 percent to 47 percent, and the average number of medications prescribed per treated patient rose from 1.14 to 1.63. 
By 2007, biguanides (54 percent of treatment visits) and glitazones (28 percent of visits) were leading therapeutic classes. Increasing use of glitazones, newer insulins, sitag...</description>
            <author>Pharmalot</author>
            <type>blogs</type>
        <comments>http://www.medworm.com/rss/comments.php?id=1969317</comments>
            <pubDate>Tue, 18 Nov 2008 20:11:19 +0100</pubDate>
            <guid isPermaLink="false">1969317</guid>        </item>
        <item>
            <title>Which Drug Web Sites Are Most Widely Viewed?</title>
            <link>http://www.medworm.com/index.php?rid=1871103&amp;cid=t_121576_150_f&amp;fid=35777&amp;url=http%3A%2F%2Ffeeds.feedburner.com%2F%7Er%2FPharmalot%2F%7E3%2F416933478%2F</link>
            <description>Would you be surprised if the answer is AstraZeneca&amp;#8217;s Nexium? The web site for the heartburn med, known as purplepill.com, generated the most site traffic in this year&amp;#8217;s second quarter, with more than 1 million unique visitors, a 55 percent increase from a year earlier. Runners-up include sites for Takeda&amp;#8217;s Actos diabetes drug and the Sanofi-Aventis Ambien CR sleeping pill. 
&amp;#8220;AstraZeneca has aggressively marketed Nexium this year, running approximately twice as much online display advertising in Q2 as either of its major competitors, Prevacid and Aciphex,” John Mangano, senior director of comScore, says in a statement. “This additional marketing muscle appears to have helped generate strong site visitation.&amp;#8221; (Source: Pharmalot)</description>
            <author>Pharmalot</author>
            <type>blogs</type>
        <comments>http://www.medworm.com/rss/comments.php?id=1871103</comments>
            <pubDate>Fri, 10 Oct 2008 16:20:21 +0100</pubDate>
            <guid isPermaLink="false">1871103</guid>        </item>
        <item>
            <title>Takeda - alogliptin: delay.....hmmm!</title>
            <link>http://www.medworm.com/index.php?rid=1865474&amp;cid=t_121576_150_f&amp;fid=34768&amp;url=http%3A%2F%2Fpharmagossip.blogspot.com%2F2008%2F10%2Ftakeda-alogliptin-delayhmmm.html</link>
            <description>Takeda, Japan's biggest drugmaker, said on Friday that U.S. health authorities have not been able to complete a review of alogliptin or SYR-322, which is critical to Takeda's mainstay diabetes business as it is expected to be the main replacement for its best-selling Actos.Actos generates almost 30 percent of Takeda's sales but loses U.S. patent protection in 2011.More (Source: PharmaGossip)</description>
            <author>PharmaGossip</author>
            <type>blogs</type>
        <comments>http://www.medworm.com/rss/comments.php?id=1865474</comments>
            <pubDate>Fri, 10 Oct 2008 10:02:00 +0100</pubDate>
            <guid isPermaLink="false">1865474</guid>        </item>
        <item>
            <title>Actos and Avandia- yes or no?</title>
            <link>http://www.medworm.com/index.php?rid=1750366&amp;cid=t_121576_134_f&amp;fid=36049&amp;url=http%3A%2F%2Ffeeds.b5media.com%2F%7Er%2Fb5media%2FDiabetesNotes%2F%7E3%2FeRv5j_-NK6s%2F</link>
            <description>Will you continue to take Avandia or Actos regardless of the new findings?
		
		
		
			
					
					Yes, it works for me
			
			
					
					I will follow my doctors advice
			
			
					
					No- way!
			
			
					
					I already stopped taking it
			
		
			
			
			
			View Results
		
		
	
Share This (Source: Diabetes Notes)</description>
            <author>Diabetes Notes</author>
            <type>blogs</type>
        <comments>http://www.medworm.com/rss/comments.php?id=1750366</comments>
            <pubDate>Sun, 31 Aug 2008 22:48:12 +0100</pubDate>
            <guid isPermaLink="false">1750366</guid>        </item>
        <item>
            <title>Questions about Actos and Avandia arise again</title>
            <link>http://www.medworm.com/index.php?rid=1750367&amp;cid=t_121576_134_f&amp;fid=36049&amp;url=http%3A%2F%2Ffeeds.b5media.com%2F%7Er%2Fb5media%2FDiabetesNotes%2F%7E3%2F4bwMuuz-7Ac%2F</link>
            <description>Over 20% of all diabetics have heart disease. That is why it is so scary when new research and studies come out that prove diabetic medication to harm your heart. And here we go again… Two Wake Forest University School of Medicine faculty members sifted through three trials to come to the conclusion that certain diabetic medications could cause increased heart failure- ACCORD, ADVANCE, and the Veterans Affairs Diabetes study.
“We strongly recommend restrictions in the use of thiazolidinediones (the class of drugs) and question the rationale for leaving rosiglitazone on the market,” write Sonal Singh, M.D., M.P.H., assistant professor of internal medicine, and Curt D. Furberg, M.D., Ph.D., professor of public health sciences. Rosiglitazone and pioglitazone are the two major thiazolidi...</description>
            <author>Diabetes Notes</author>
            <type>blogs</type>
        <comments>http://www.medworm.com/rss/comments.php?id=1750367</comments>
            <pubDate>Sun, 31 Aug 2008 22:44:53 +0100</pubDate>
            <guid isPermaLink="false">1750367</guid>        </item>
        <item>
            <title>Actos and Avandia being linked to increased heart failure</title>
            <link>http://www.medworm.com/index.php?rid=1742862&amp;cid=t_121576_111_f&amp;fid=36048&amp;url=http%3A%2F%2Ffeeds.b5media.com%2F%7Er%2Fb5media%2FAHeartyLife%2F%7E3%2FJsarMrAGxFA%2F</link>
            <description>Over 20% of all diabetics have heart disease. That is why it is so scary when new research and studies come out that prove diabetic medication to harm your heart. And here we go again&amp;#8230; Two Wake Forest University School of Medicine faculty members sifted through three trials to come to the conclusion that certain diabetic medications could cause increased heart failure- ACCORD, ADVANCE, and the Veterans Affairs Diabetes study.
&amp;#8220;We strongly recommend restrictions in the use of thiazolidinediones (the class of drugs) and question the rationale for leaving rosiglitazone on the market,&amp;#8221; write Sonal Singh, M.D., M.P.H., assistant professor of internal medicine, and Curt D. Furberg, M.D., Ph.D., professor of public health sciences. Rosiglitazone and pioglitazone are the two majo...</description>
            <author>A Hearty Life</author>
            <type>blogs</type>
        <comments>http://www.medworm.com/rss/comments.php?id=1742862</comments>
            <pubDate>Fri, 29 Aug 2008 16:03:53 +0100</pubDate>
            <guid isPermaLink="false">1742862</guid>        </item>
        <item>
            <title>Glitazones - the heart of the matter</title>
            <link>http://www.medworm.com/index.php?rid=1739100&amp;cid=t_121576_150_f&amp;fid=34768&amp;url=http%3A%2F%2Fpharmagossip.blogspot.com%2F2008%2F08%2Fglitazones-heart-of-matter.html</link>
            <description>A class of oral drugs used to treat type 2 diabetes may make heart failure worse, according to an editorial published online in Heart Wednesday by two Wake Forest University School of Medicine faculty members.“We strongly recommend restrictions in the use of thiazolidinediones (the class of drugs) and question the rationale for leaving rosiglitazone on the market,” write Sonal Singh, M.D., M.P.H., assistant professor of internal medicine, and Curt D. Furberg, M.D., Ph.D., professor of public health sciences. Rosiglitazone and pioglitazone are the two major thiazolidinediones.In the editorial Singh and Furberg say, “At this time, justification for use of thiazolidinediones is very weak to non-existent.”Oral drugs are given to control diabetes by lowering blood sugar.But diabetics al...</description>
            <author>PharmaGossip</author>
            <type>blogs</type>
        <comments>http://www.medworm.com/rss/comments.php?id=1739100</comments>
            <pubDate>Fri, 29 Aug 2008 05:12:00 +0100</pubDate>
            <guid isPermaLink="false">1739100</guid>        </item>
        <item>
            <title>Which Drug Websites Do Doctors Visit The Most?</title>
            <link>http://www.medworm.com/index.php?rid=1734255&amp;cid=t_121576_150_f&amp;fid=35777&amp;url=http%3A%2F%2Ffeeds.feedburner.com%2F%7Er%2FPharmalot%2F%7E3%2F375230213%2F</link>
            <description>The sites that feature diabetes meds top the list, with Merck&amp;#8217;s Januvia garnering the No. 1 ranking and Takeda Pharmaceutical&amp;#8217;s Actos finishing second, according to Manhattan Research, which says it conducted an online survey in this year&amp;#8217;s second quarter of 1,681 docs practicing in the US.
Interestingly, the research firm says that more docs are visiting sites for controversial drugs - Pfizer&amp;#8217;s Chantix smoking-cessation pill and Merck&amp;#8217;s Gardasil vaccine for HPV. Actos, by the way, crashed the list for the first time, perhaps reflecting the problems with a rival diabetes pill, Glaxo&amp;#8217;s Avandia.
1.           Januvia
2.           Actos
3.           Chantix
4.           Gardasil
5.           Actonel
6.           Vytorin
7.           Amitiza
8.           Byet...</description>
            <author>Pharmalot</author>
            <type>blogs</type>
        <comments>http://www.medworm.com/rss/comments.php?id=1734255</comments>
            <pubDate>Tue, 26 Aug 2008 12:44:29 +0100</pubDate>
            <guid isPermaLink="false">1734255</guid>        </item>
        <item>
            <title>The Black Box Warning: Is The FDA Overreacting?</title>
            <link>http://www.medworm.com/index.php?rid=1625797&amp;cid=t_121576_150_f&amp;fid=35777&amp;url=http%3A%2F%2Ffeeds.feedburner.com%2F%7Er%2FPharmalot%2F%7E3%2F336156450%2F</link>
            <description>Last week, an FDA advisory committee voted that 11 epilepsy meds can increase the risk of suicide, but voted 14-4 against adding a Black Box about those risks on the drug labeling, something the agency itself suggested several times in the weeks leading to the meeting.
The episode followed a spate of new or revised Black Box warnings - the most serious warning the FDA can recommend a drugmaker place on product labeling - for a host of drugs over the past few years. These include antidepressants, antipsychotics, antibiotics, anemia treatments, ultrasound meds, asthma drugs and diabetes pills (have we forgotten anything? Send us a note).
The recent vote over epilepsy meds prompted speculation that, perhaps, the FDA has become so painfully aware of safety concerns that the Black Box warning i...</description>
            <author>Pharmalot</author>
            <type>blogs</type>
        <comments>http://www.medworm.com/rss/comments.php?id=1625797</comments>
            <pubDate>Tue, 15 Jul 2008 14:43:15 +0100</pubDate>
            <guid isPermaLink="false">1625797</guid>        </item>
        <item>
            <title>Takeda Pharmaceuticals' Actos</title>
            <link>http://www.medworm.com/index.php?rid=1475234&amp;cid=t_121576_97_f&amp;fid=35050&amp;url=http%3A%2F%2Ffeeds.feedburner.com%2F%7Er%2FPharmaGazette%2F%7E3%2F299245434%2Ftakeda_pharmaceuticals_actos.html</link>
            <description>Actos (pioglitazone hydrocloride) manufactured by Takeda Pharmaceuticals,&amp;nbsp;is a once-daily oral medication that helps control blood sugar levels in patients with Type 2 diabetes.Actos works by reducing insulin resistance which is a condition where the body&amp;#39;s cells do not respond to the hormone insulin that allows them to turn blood sugar into energy. When used in conjunction with proper diet and exercise the medication can be effective achieving glycemic control.Contact your health care provider if you experience any of the following side effects: nausea, vomiting, stomach pain, loss of energy, loss of appetite, dark urine, or jaundice. Also report any rapid weight gain, retention of water, shortness of breath or any other symptoms of heart failure.In June 2007 the U.S. Food and Dr...</description>
            <author>PharmaGazette</author>
            <type>blogs</type>
        <comments>http://www.medworm.com/rss/comments.php?id=1475234</comments>
            <pubDate>Tue, 27 May 2008 18:00:22 +0100</pubDate>
            <guid isPermaLink="false">1475234</guid>        </item>
        <item>
            <title>Pharmalot… Pharmalittle… Good Morning</title>
            <link>http://www.medworm.com/index.php?rid=1129500&amp;cid=t_121576_150_f&amp;fid=35777&amp;url=http%3A%2F%2Ffeeds.feedburner.com%2F%7Er%2FPharmalot%2F%7E3%2F211087445%2F</link>
            <description>The short work week is drawing to a close. By now, though, you most likely have settled back into your routine. We know we have. As you ready for the next meeting and report, grab a cup of something hot and catch up with these&amp;#8230;
Takeda Seeks FDA Approval For Actos Follow-Up (Bloomberg News)
Sanofi Pooh-Poohs Lawsuit Charging Acomplia Data Was Hidden (Reuters)
Drugmakers Vie For Magic Weight-Loss Pill (MSNBC/AP)
Share / E-mail (Source: Pharmalot)</description>
            <author>Pharmalot</author>
            <type>blogs</type>
        <comments>http://www.medworm.com/rss/comments.php?id=1129500</comments>
            <pubDate>Fri, 04 Jan 2008 12:11:26 +0100</pubDate>
            <guid isPermaLink="false">1129500</guid>        </item>
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            <title>Actos is Dangerous Too!</title>
            <link>http://www.medworm.com/index.php?rid=1090505&amp;cid=t_121576_134_f&amp;fid=35137&amp;url=http%3A%2F%2Fdiabetesupdate.blogspot.com%2F2007%2F12%2Factos-is-dangerous-too.html</link>
            <description>If you follow the diabetes news, you probably saw reports today about a new study published in the Journal of the American Medical Association, this one, a study of the medical records of people over 65, is being reported as it if found that Avandia raised the rate of heart attacks and death. That is how the New York Times and many other news organizations are headlining this story. But that isn't actually what the study found. Here's a better report.Study: Type 2 diabetes drugs raise heart risks: Chicago Tribute based on study published in JAMA The crucial piece of information here is that, in a study of patient records of people over 65 taking various diabetes drugs both TZD drugs, Avandia and Actos, appeared to cause significant increases in death and heart problems. I can't help but wo...</description>
            <author>Diabetes Update</author>
            <type>blogs</type>
        <comments>http://www.medworm.com/rss/comments.php?id=1090505</comments>
            <pubDate>Wed, 12 Dec 2007 15:59:00 +0100</pubDate>
            <guid isPermaLink="false">1090505</guid>        </item>
        <item>
            <title>Avandia And Actos Linked To Heart Risks</title>
            <link>http://www.medworm.com/index.php?rid=1087709&amp;cid=t_121576_150_f&amp;fid=35777&amp;url=http%3A%2F%2Ffeeds.feedburner.com%2F%7Er%2FPharmalot%2F%7E3%2F198889436%2F</link>
            <description>Yet another study suggests problems with Avandia. This time, however, Actos also gets tagged. An article published in this week&amp;#8217;s edition of the Journal of the American Medical Association concludes the two drugs pose a significantly greater risk of heart attack, congestive heart failure and death in older patients compared with other diabetes meds. (This is the abstract).
This is only the latest difficulty for Glaxo, which has seen Avandia sales plummet this year following a controversial meta-analysis last spring that linked the drug to an increased risk of heart attacks. The FDA allowed the pill to remain on the market, but slapped a second Black Box warning on the labeling. The troubles facing the med, which was once a best seller, is now cited as a key reason for Glaxo&amp;#8217;s p...</description>
            <author>Pharmalot</author>
            <type>blogs</type>
        <comments>http://www.medworm.com/rss/comments.php?id=1087709</comments>
            <pubDate>Tue, 11 Dec 2007 23:30:55 +0100</pubDate>
            <guid isPermaLink="false">1087709</guid>        </item>
        <item>
            <title>Drug Warnings and Withdrawls for 2007</title>
            <link>http://www.medworm.com/index.php?rid=1072405&amp;cid=t_121576_97_f&amp;fid=35050&amp;url=http%3A%2F%2Ffeeds.feedburner.com%2F%7Er%2FPharmaGazette%2F%7E3%2F195737938%2Fdrug_warnings_and_withdrawls_f_1.html</link>
            <description>FiercePharma has compiled a list of the top 10 drugs to have&amp;nbsp;who have had approval&amp;nbsp;either withdrawn or been forced to add stronger warning labels, by the FDA, with respect to their pharmaceutical products.&amp;nbsp; The list is based on 2006 worldwide sales so ranking does not necessarily include the big new makers.1. Antidepressants - Various companies - &amp;quot;Black&amp;quot; box warning regarding increased risk of suicidal thoughts.2. Epogen/Aranesp - Amgen - &amp;quot;Black&amp;quot; box warning of heart and vascular risk at higher doses3. Zyprexa - Lilly - Warning of weight gain and metabolic problems4. Avandia - Glaxo - &amp;quot;Black&amp;quot; box warning of heart failure and heart attack5. Actos - Takeda - &amp;quot;Black&amp;quot; box warning of heart failure6. Provigil - Cephalon - Waning of Stevens-J...</description>
            <author>PharmaGazette</author>
            <type>blogs</type>
        <comments>http://www.medworm.com/rss/comments.php?id=1072405</comments>
            <pubDate>Wed, 05 Dec 2007 20:00:41 +0100</pubDate>
            <guid isPermaLink="false">1072405</guid>        </item>
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            <title>Takeda Pharmaceuticals' Actos Gets Stronger FDA Warning</title>
            <link>http://www.medworm.com/index.php?rid=1072409&amp;cid=t_121576_97_f&amp;fid=35050&amp;url=http%3A%2F%2Ffeeds.feedburner.com%2F%7Er%2FPharmaGazette%2F%7E3%2F195622211%2Ftakeda_pharmaceuticals_actos_g.html</link>
            <description>In June 2007, during congressional hearings, the U.S. Food and Drug Administration revealed that it has called for the strongest black box warning possible on Actos.After reviewing postmarketing adverse event reports, the FDA that&amp;nbsp;Actos (pioglitazone), approved to treat Type 2 diabetes, required a black box warning emphasizing that the drug may cause or worsen heart failure in certain patients. The warning covers all thiazolidinedone class drugs including Avandia, Actos, Avandaryl, Avandamet and Duetact.&amp;quot;Under FDA&amp;#39;s postmarketing surveillance program, we carefully monitor new safety information for marketed drugs and take appropriate action when necessary to inform patients and health care providers of new information,&amp;quot; said Steven Galson, M.D., M.P.H., director of FDA&amp;#...</description>
            <author>PharmaGazette</author>
            <type>blogs</type>
        <comments>http://www.medworm.com/rss/comments.php?id=1072409</comments>
            <pubDate>Wed, 05 Dec 2007 16:00:21 +0100</pubDate>
            <guid isPermaLink="false">1072409</guid>        </item>
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            <title>A Big Year For Big Warnings And Withdrawals</title>
            <link>http://www.medworm.com/index.php?rid=1068797&amp;cid=t_121576_150_f&amp;fid=35777&amp;url=http%3A%2F%2Ffeeds.feedburner.com%2F%7Er%2FPharmalot%2F%7E3%2F194961311%2F</link>
            <description>In case you missed it, this has been quite a year for high-profile safety news. And so FiercePharma has compiled a list for the cocktail set, who want to keep track of such things. These are the 10 biggest drugs that were withdrawn or were issued new warnings by the FDA this year. The drugs are ranked by 2006 worldwide sales, which explains why such headline grabbers as Bayer&amp;#8217;s Trasylol doesn&amp;#8217;t appear - sales were already tanking on bad news.
1. Antidepressants - Various companies 
2. Epogen/Aranesp - Amgen 
3. Zyprexa - Lilly 
4. Avandia - Glaxo
5. Actos - Takeda 
6. Provigil - Cephalon 
7. Zelnorm - Novartis 
8. Byetta - Amylin 
9. Xolair - Genentech 
10. Fentora - Cephalon 
Source: FiercePharma
Share / E-mail (Source: Pharmalot)</description>
            <author>Pharmalot</author>
            <type>blogs</type>
        <comments>http://www.medworm.com/rss/comments.php?id=1068797</comments>
            <pubDate>Tue, 04 Dec 2007 14:15:23 +0100</pubDate>
            <guid isPermaLink="false">1068797</guid>        </item>
        <item>
            <title>Avandia Causes Osteoporosis and Broken Bones--But Actos Does TOO!</title>
            <link>http://www.medworm.com/index.php?rid=1067812&amp;cid=t_121576_134_f&amp;fid=35137&amp;url=http%3A%2F%2Fdiabetesupdate.blogspot.com%2F2007%2F12%2Favandia-causes-osteoporosis-but-actos.html</link>
            <description>This week's medical news is full of reports about a study that explains why Avandia causes osteoporosis. Here's a report that gives more than the usual amount of detail about this study:Avandia Researchers Find Reason Behind Bone Fracture, Osteoporosis Side Effectshttp://www.newsinferno.com/archives/2123I have already blogged about Avandia's connection with a doubling of the incidence of fractures this last year HERE.But what concerns me now is that the way this new story is being reported makes it sound as if the osteoporosis is only a side effect of Avandia, a drug that for all practical purposes is dead after the press discovered the long-known fact that research proved it increases heart attacks. But as the article I link above makes clear, the reason Avandia causes the bones to thin i...</description>
            <author>Diabetes Update</author>
            <type>blogs</type>
        <comments>http://www.medworm.com/rss/comments.php?id=1067812</comments>
            <pubDate>Mon, 03 Dec 2007 17:09:00 +0100</pubDate>
            <guid isPermaLink="false">1067812</guid>        </item>
        <item>
            <title>Pharmalot… Pharmalittle… Rise And Shine</title>
            <link>http://www.medworm.com/index.php?rid=1055790&amp;cid=t_121576_150_f&amp;fid=35777&amp;url=http%3A%2F%2Ffeeds.feedburner.com%2F%7Er%2FPharmalot%2F%7E3%2F191810593%2F</link>
            <description>As we awake, we are reminded of the old adage, articulated regularly by a former morning mayor, that every brand new day should be unwrapped like a precious gift. And so we are in the process of gently pulling back the covering and celebrating our good fortune. We hope you do the same&amp;#8230;
EU And US Docs Urge More Cautious Use Of Diabetes Meds (Yahoo/Reuters)
GPC Biotech Seeks A Merger Partner (Bloomberg News)
Canada&amp;#8217;s QLT Puts Itself Up For Sale (Yahoo/Reuters)
Novartis Says EU Approves Tasigna (Yahoo/Reuters)
Merck KgGA Starts Phase III On Parkinson&amp;#8217;s Drug (CNNMoney.com/Thomson)
Share / E-mail (Source: Pharmalot)</description>
            <author>Pharmalot</author>
            <type>blogs</type>
        <comments>http://www.medworm.com/rss/comments.php?id=1055790</comments>
            <pubDate>Wed, 28 Nov 2007 12:24:23 +0100</pubDate>
            <guid isPermaLink="false">1055790</guid>        </item>
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            <title>Takeda Exploits Avandia Woes With New Ads</title>
            <link>http://www.medworm.com/index.php?rid=1030257&amp;cid=t_121576_150_f&amp;fid=35777&amp;url=http%3A%2F%2Ffeeds.feedburner.com%2F%7Er%2FPharmalot%2F%7E3%2F185452818%2F</link>
            <description>It would only be surprising if Takeda Pharmaceuticals didn&amp;#8217;t make such a move. The drugmaker plans to roll out ads touting the safety of its own Actos diabetes pills tomorrow - just two days after Glaxo acquiesced to the FDA and agreed to place yet another Black Box warning on Avandia product labeling. The new warning carries info about heart attack risks; an earlier Black Box mentions heart failure.
Although the latest Avandia warning says that evidence is &amp;#8220;inconclusive&amp;#8221; about the increased risk of heart attacks, Wall Street expects the language to further dampen sales of the drug, which have plummeted since safety concerns arose in May, the Associated Press notes. And this gives Actos an advantage, because its the only diabetes drug in the same class as Avandia. Takeda ...</description>
            <author>Pharmalot</author>
            <type>blogs</type>
        <comments>http://www.medworm.com/rss/comments.php?id=1030257</comments>
            <pubDate>Thu, 15 Nov 2007 23:26:40 +0100</pubDate>
            <guid isPermaLink="false">1030257</guid>        </item>
        <item>
            <title>Pharmalot… Pharmalittle… Good Morning</title>
            <link>http://www.medworm.com/index.php?rid=1003709&amp;cid=t_121576_150_f&amp;fid=35777&amp;url=http%3A%2F%2Ffeeds.feedburner.com%2F%7Er%2FPharmalot%2F%7E3%2F180031756%2F</link>
            <description>A busy morning here in the nation&amp;#8217;s medicine chest. We expect to debut the bus ads from the Provenge protesters and the FDA is about to hold a teleconference call to discuss the suspension of Bayer&amp;#8217;s Trayslol. Meanwhile, we hope these will get you through the re-entry process&amp;#8230; 
Novacea Halts Prostate-Cancer Drug Trial Over Deaths (Yahoo/Reuters)
Takeda Predicts Big Profits Thanks To Actos (Bloomberg News)
Less Is More With Schering-Plough Clot Drug (Yahoo/Reuters)
Sweep Of Lung Cancer Genome Yields New Gene (Yahoo/Reuters)
Combo Drug Approvals Cause Spat In India (Hindu Business Online)
South Africa Looks To Boost Pharma Sector (Business Report)
FDA Rejects Glaxo&amp;#8217;s Gepirone ER Antidepressant (Yahoo/Reuters)
Share / E-mail (Source: Pharmalot)</description>
            <author>Pharmalot</author>
            <type>blogs</type>
        <comments>http://www.medworm.com/rss/comments.php?id=1003709</comments>
            <pubDate>Mon, 05 Nov 2007 11:38:08 +0100</pubDate>
            <guid isPermaLink="false">1003709</guid>        </item>
        <item>
            <title>Avandia To Get Another Black Box Warning?</title>
            <link>http://www.medworm.com/index.php?rid=974715&amp;cid=t_121576_150_f&amp;fid=35777&amp;url=http%3A%2F%2Ffeeds.feedburner.com%2F%7Er%2FPharmalot%2F%7E3%2F174274876%2F</link>
            <description>Glaxo&amp;#8217;s diabetes pill already has such a warning about heart failure, but apparently the FDA wants to add one about the risk of heart attacks, according to The Wall Street Journal. Talks are still under way, the paper writes, but if agency officials succeed, the move would make it still more difficult for sales to rebound. 
Ever since the New England Journal of Medicine published a study last May that Avandia raised the risk of heart attacks by 43 percent, the drugmaker has insisted evidence is lacking that the diabetes pill is more dangerous than rival meds. Avandia scrips, meanwhile, have continued to plunge and sales were down 38 percent in the third quarter. As the paper notes, Takeda&amp;#8217;s Actos also carries a warning about the risk of heart failure, but not heart attack.
An F...</description>
            <author>Pharmalot</author>
            <type>blogs</type>
        <comments>http://www.medworm.com/rss/comments.php?id=974715</comments>
            <pubDate>Wed, 24 Oct 2007 11:30:48 +0100</pubDate>
            <guid isPermaLink="false">974715</guid>        </item>
        <item>
            <title>Actos Better than Avandia study Confirms</title>
            <link>http://www.medworm.com/index.php?rid=894217&amp;cid=t_121576_97_f&amp;fid=35050&amp;url=http%3A%2F%2Ffeeds.feedburner.com%2F%7Er%2FPharmaGazette%2F%7E3%2F160326364%2Factos_better_than_avandia_study_confirms.html</link>
            <description>Clinical trials results have found that patients receiving a starting dose&amp;nbsp;of Takeda Pharmaceutical&amp;#39;s diabetes drug, Actos gain better control of blood sugar and lipid levels than those using GlaxoSmithKline&amp;#39;s Avandia.This finding comes on the heels of recent fears that Avandia increases heart attack risks. The findings are form the first 3 months of a 6 month study that pitted a 30 milligram dose of Actos against a 4 milligram dose of Avandia. Results were that Actos significantly reduced triglyceride and LDL cholesterol and increased levels of HDL cholesterol.&amp;quot;A likely explanation for the different effects on heart attack and strokes between the two drugs could be the favorable effect of pioglitazone in increasing HDL cholesterol without adverse effects on LDL as demons...</description>
            <author>PharmaGazette</author>
            <type>blogs</type>
        <comments>http://www.medworm.com/rss/comments.php?id=894217</comments>
            <pubDate>Sun, 23 Sep 2007 19:50:09 +0100</pubDate>
            <guid isPermaLink="false">894217</guid>        </item>
        <item>
            <title>Actos - The New Fad</title>
            <link>http://www.medworm.com/index.php?rid=870469&amp;cid=t_121576_133_f&amp;fid=35109&amp;url=http%3A%2F%2Fwww.kevinleitch.co.uk%2Fwp%2F%3Fp%3D622</link>
            <description>Conclusion: Pioglitazone should be considered for further testing of therapeutic potential in autistic patients.

	Happy days right?

	Well of course not. Would I be blogging about it if it was?

	First problem I thought of was the discrepancy between sample size (25) and conclusion. At best I would think of this as a pilot study.

	The second issue was the utter lack of clarification regarding Actos and what exact risks were spelled out to the patients or their guardians. Actos is pretty heavy stuff.

	Last week Actos received a &amp;#8220;black box warning&amp;#8221; from the U.S. Food and Drug Administration, the agency&amp;#8217;s strongest level of caution. Actos, and a similar diabetes drug, Avandia, can increase the risk of heart failure, the FDA warned.

	A black box warning means that the dru...</description>
            <author>Left Brain/Right Brain</author>
            <type>blogs</type>
        <comments>http://www.medworm.com/rss/comments.php?id=870469</comments>
            <pubDate>Fri, 14 Sep 2007 09:55:34 +0100</pubDate>
            <guid isPermaLink="false">870469</guid>        </item>
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            <title>Heart Risks: Avandia Is Higher Than Actos</title>
            <link>http://www.medworm.com/index.php?rid=864405&amp;cid=t_121576_150_f&amp;fid=35777&amp;url=http%3A%2F%2Ffeeds.feedburner.com%2F%7Er%2FPharmalot%2F%7E3%2F155205504%2F</link>
            <description>More trouble for Glaxo. New studies in the Journal of the American Medical Association say that Avandia increased the chances of having a heart attack, while Takeda&amp;#8217;s competing drug lowered the risk. The Glaxo pill increased heart attacks by 42 percent and doubled rates of heart failure. Takeda&amp;#8217;s Actos reduced heart attacks, strokes and deaths by 18 percent, though it also increased heart failure, according to a separate study funded by the drugmaker. 
There&amp;#8217;s little doubt this will make it much more difficult for Glaxo to win back market share. Avandia was the world&amp;#8217;s best-selling diabetes pill until May, when a controversial study was reported by the Cleveland Clinic&amp;#8217;s Steve Nissen in The New England Journal of Medicine that the pill increased heart attack r...</description>
            <author>Pharmalot</author>
            <type>blogs</type>
        <comments>http://www.medworm.com/rss/comments.php?id=864405</comments>
            <pubDate>Tue, 11 Sep 2007 21:24:36 +0100</pubDate>
            <guid isPermaLink="false">864405</guid>        </item>
        <item>
            <title>Type 2 drug prescribed for autism</title>
            <link>http://www.medworm.com/index.php?rid=821979&amp;cid=t_121576_87_f&amp;fid=34867&amp;url=http%3A%2F%2Fwww.thediabetesblog.com%2F2007%2F08%2F25%2Ftype-2-drug-prescribed-for-autism%2F</link>
            <description>Filed under: Type 2, Childhood, Adult Onset, DrugsAutism is a bio-neurological disorder typically appearing in children before the age of 3. Individuals with autism usually have difficulties in verbal and non-verbal communication, social interaction, play and cognitive function, as well as certain physical ailments. Severity of autism can vary widely. One in 150 now have autism, and boys are diagnosed four times more often than girls.
Alternative treatments for autism are growing (chelation and dietary therapies), but I've never heard of this one -- the type 2 diabetes drug Actos. Dr. Marvin Boris of Autism Associates, stated his office prescribes Actos to children with autism. Remember, Actos just received the black box warning from the Food and Drug Administration for risk of heart failu...</description>
            <author>The Diabetes Blog</author>
            <type>blogs</type>
        <comments>http://www.medworm.com/rss/comments.php?id=821979</comments>
            <pubDate>Sat, 25 Aug 2007 04:00:00 +0100</pubDate>
            <guid isPermaLink="false">821979</guid>        </item>
        <item>
            <title>Avandia And Actos Get A Black Box</title>
            <link>http://www.medworm.com/index.php?rid=799395&amp;cid=t_121576_150_f&amp;fid=35777&amp;url=http%3A%2F%2Ffeeds.feedburner.com%2F%7Er%2FPharmalot%2F%7E3%2F144157126%2F</link>
            <description>This isn&amp;#8217;t surprising, is it? The stronger warning about the risk of heart failure will, in fact, be added to the labels for an entire class of type 2 diabetes drugs, which also includes Avandaryl, Avandamet and Duetact. The move, announced by the FDA, comes after the July 30 advisory committee meeting, in which stronger warnings and restrictions were recommended. 
“This new boxed warning addresses FDA’s concerns that despite the warnings and information already listed in the drug labels, these drugs are still being prescribed to patients without careful monitoring for signs of heart failure,” says Steve Galson, director of the FDA&amp;#8217;s Center for Drug Evaluation and Research.
The agency&amp;#8217;s review of adverse event reports found an unspecified number of cases of signific...</description>
            <author>Pharmalot</author>
            <type>blogs</type>
        <comments>http://www.medworm.com/rss/comments.php?id=799395</comments>
            <pubDate>Tue, 14 Aug 2007 21:09:29 +0100</pubDate>
            <guid isPermaLink="false">799395</guid>        </item>
        <item>
            <title>Steve Nissen Talks About Avandia, Again</title>
            <link>http://www.medworm.com/index.php?rid=783158&amp;cid=t_121576_150_f&amp;fid=35777&amp;url=http%3A%2F%2Ffeeds.feedburner.com%2F%7Er%2FPharmalot%2F%7E3%2F141304974%2F</link>
            <description>The Pink Sheet, the venerable trade publication, conducted an interesting question-and-answer interview with the controversial Cleveland Clinic cardiologist after the recent FDA advisory panel meeting, in which new, but unspecified restrictions were recommended for the Glaxo diabetes drug. This is an excerpt of what he had to say about clinical trial design, advisory panels and safety issues&amp;#8230;.
The Pink Sheet: What is the proper role of meta-analyses in drug safety oversight, and is that role changing?
Steven Nissen: A meta-analysis is a fine way to assess the safety of a drug - it&amp;#8217;s not necessarily the best way to assess the efficacy of a drug. I actually thought the committee maybe didn&amp;#8217;t understand that. [To] put it into perspective, what the FDA did in their meta-analy...</description>
            <author>Pharmalot</author>
            <type>blogs</type>
        <comments>http://www.medworm.com/rss/comments.php?id=783158</comments>
            <pubDate>Mon, 06 Aug 2007 18:49:23 +0100</pubDate>
            <guid isPermaLink="false">783158</guid>        </item>
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            <title>Pharmalot… Pharmalittle… Evening Edition</title>
            <link>http://www.medworm.com/index.php?rid=767706&amp;cid=t_121576_150_f&amp;fid=35777&amp;url=http%3A%2F%2Ffeeds.feedburner.com%2F%7Er%2FPharmalot%2F%7E3%2F139022484%2F</link>
            <description>A busy day, thanks primarily to Avandia, of course. Who says the summer is a slow time? There&amp;#8217;s always a lot of pharma, as our name implies. With that in mind, here are a few items to tide you over until the morning approaches&amp;#8230;
Patients taking Takeda&amp;#8217;s Actos diabetes drug were less likely to suffer a heart attack or need their arteries cleared than those taking Glaxo&amp;#8217;s Avandia, a new study finds. The study was discussed at today&amp;#8217;s FDA advisory panel meeting to review Avandia. You can read more at Bloomberg News.
The difficulties in generating, and relying on, a meta-analysis are discussed in a piece by BusinessWeek. The issuey illustrates the hard choices researchers must make when analyzing batches of studies. &amp;#8220;The biggest issue is how to go about selec...</description>
            <author>Pharmalot</author>
            <type>blogs</type>
        <comments>http://www.medworm.com/rss/comments.php?id=767706</comments>
            <pubDate>Tue, 31 Jul 2007 00:41:47 +0100</pubDate>
            <guid isPermaLink="false">767706</guid>        </item>
        <item>
            <title>Avandia And Actos Double Heart-Failure Risk</title>
            <link>http://www.medworm.com/index.php?rid=761705&amp;cid=t_121576_150_f&amp;fid=35777&amp;url=http%3A%2F%2Ffeeds.feedburner.com%2F%7Er%2FPharmalot%2F%7E3%2F137934060%2F</link>
            <description>Yet another meta-analysis finds Glaxo&amp;#8217;s diabetes drug is trouble - and finds the same thing about Takeda&amp;#8217;s Actos, too. The analysis reviewed more than 78,000 patients, and estimates that one in every 50 patients taking the drugs over a 26-month period will require hospital admission due to heart failure, PharmaTimes reports.
“This means that the diabetes drugs could have caused thousands of additional cases of heart failure, creating a substantial burden on hard-pressed health services,” says Yoon Loke, a clinical pharmacologist at UEA’s School of Medicine, Health Policy and Practice. The results are being published in the August edition of the journal Diabetes Care.
The news comes on the eve of this Monday&amp;#8217;s FDA panel meeting to decide whether Avandia should be yan...</description>
            <author>Pharmalot</author>
            <type>blogs</type>
        <comments>http://www.medworm.com/rss/comments.php?id=761705</comments>
            <pubDate>Fri, 27 Jul 2007 12:02:01 +0100</pubDate>
            <guid isPermaLink="false">761705</guid>        </item>
        <item>
            <title>Old-Time Meds Beat Avandia And Actos</title>
            <link>http://www.medworm.com/index.php?rid=737688&amp;cid=t_121576_150_f&amp;fid=35777&amp;url=http%3A%2F%2Ffeeds.feedburner.com%2F%7Er%2FPharmalot%2F%7E3%2F134352106%2F</link>
            <description>Like to save money and avoid health risks? Try an older diabetes med. Avandia and Actos are no more effective at controlling diabetes, and are often less safe than older meds that cost much less, according to a new report by Consumers Report. For instance, the newer meds can cost $150 to $250 a month, compared with $10 to $60 a month for older drugs, such as metformin.
“This is truly significant information for the millions of people with diabetes struggling to control their disease, but also struggling with the high cost of their medications,” says Gail Shearer, project director of Consumer Reports&amp;#8217; Best Buy Drugs. “The evidence shows that lower-cost, older medicines work just as well for most people.” You can read the full report here.
The report is based on a new analysis ...</description>
            <author>Pharmalot</author>
            <type>blogs</type>
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            <pubDate>Mon, 16 Jul 2007 21:58:55 +0100</pubDate>
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            <title>Prescriber's Letter offers practitioners unbiased Avandia advice</title>
            <link>http://www.medworm.com/index.php?rid=682755&amp;cid=t_121576_87_f&amp;fid=34867&amp;url=http%3A%2F%2Fwww.thediabetesblog.com%2F2007%2F06%2F18%2Fprescribers-letter-offers-practitioners-unbiased-avandia-advice%2F</link>
            <description>Filed under: Type 2, Adult Onset, Drugs, ResearchAvandia is out of the top headlines lately, but I am sure the controversial drug remains top-of-mind for type 2 diabetics carrying a prescription. 
I fumbled upon Prescriber's Letter recently, an independent service providing information about meds to paid subscribers. They claim their research reports are unbiased, the website does not accept advertising (a plus) and overviews are written by editors advised by experts, government agencies and national organizations. The June edition of Prescriber's Letter offers a synopsis on Avandia. It might be worth a read. 
In a nutshell, Prescriber's acknowledges Dr. Nissen's meta-analysis which points to higher heart attack risk for Avandia versus different meds or placebos. They also acknowledge expe...</description>
            <author>The Diabetes Blog</author>
            <type>blogs</type>
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            <pubDate>Mon, 18 Jun 2007 04:00:00 +0100</pubDate>
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            <title>Januvia, Actos set to benefit from Avandia's plight</title>
            <link>http://www.medworm.com/index.php?rid=675456&amp;cid=t_121576_87_f&amp;fid=34867&amp;url=http%3A%2F%2Fwww.thediabetesblog.com%2F2007%2F06%2F13%2Fjanuvia-actos-set-to-benefit-from-avandias-plight%2F</link>
            <description>Filed under: Type 2, Drugs, ResearchAvandia, a drug used to treat Type 2 diabetes, has been in the news of late following the release of controversial study results which concluded the drug leaves patients at an increased risk for heart trouble. My fellow blogger Bev has touched on the conundrum now facing diabetics on Avandia regimens. You can quit taking Avandia, but then what? Thousands of Americans are now facing this predicament and many have opted to switch their prescriptions to something else. The Philadelphia Inquirer is running a feature about this and talks to some diabetics who have opted for the &quot;try something else&quot; route. The Inquirer profiles, among others, pharmacist Ben Briggs, 59, who switched to Merck's Januvia in the wake of the Avandia scandal, but was sorely disappoin...</description>
            <author>The Diabetes Blog</author>
            <type>blogs</type>
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            <pubDate>Wed, 13 Jun 2007 04:00:00 +0100</pubDate>
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            <title>Avandia/Actos Problems Well Known in 2003</title>
            <link>http://www.medworm.com/index.php?rid=676284&amp;cid=t_121576_134_f&amp;fid=35137&amp;url=http%3A%2F%2Fdiabetesupdate.blogspot.com%2F2007%2F06%2Favandiaactos-problems-well-known-in.html</link>
            <description>I just did a search of the alt.support.diabetes newsgroup to see when, exactly, I became aware of the significant problems with Avandia and Actos that just made the medical news this month.It was in 2003.Here are the side effects I posted about along with the date of the posting and the thread title in case you want to look up the old messages yourself. All postings were made under the username &quot;Jenny.&quot; The posted text is in italics.1. Heart Failure:Posted on a.s.d. on Oct 24, 2003. Thread name: Metformin &amp; Glyburide should I change meds?:Actos and Avandia (a similar drug) have their own problems--notably a tendency to cause weight gain and worsen heart failure. Also, they have not been on the market long enough for us to really know what their long term effects might be. They are related ...</description>
            <author>Diabetes Update</author>
            <type>blogs</type>
        <comments>http://www.medworm.com/rss/comments.php?id=676284</comments>
            <pubDate>Thu, 07 Jun 2007 16:26:00 +0100</pubDate>
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            <title>My Agenda: Why I Crusade against Dangerous Drugs</title>
            <link>http://www.medworm.com/index.php?rid=638926&amp;cid=t_121576_134_f&amp;fid=35137&amp;url=http%3A%2F%2Fdiabetesupdate.blogspot.com%2F2007%2F05%2Fmy-agenda-why-i-crusade-against.html</link>
            <description>As a result of my postings about Avandia and Actos I've been accused by the moderator of the American Diabetes Association discussion board (in a private email) of having an &quot;agenda.&quot;  Well, I do have one-- it is keeping people healthy. And as long as the American Diabetes Association continues to give patients advice that damages their health, my &quot;agenda&quot; will annoy them.The ADA's latest move was this: As soon as the news of Avandia's possible lethal side effects was broken by the far-from-hot-headed New England Journal of Medicine, the ADA immediately announced to the major media that patients should keep taking Avandia.  This response was so swift that it is not possible that anyone at the ADA had actually analyzed the findings published by the NEJM--findings, which were, as it turned o...</description>
            <author>Diabetes Update</author>
            <type>blogs</type>
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            <pubDate>Sun, 27 May 2007 11:44:00 +0100</pubDate>
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            <title>DREAM STUDY: Avandia Kills People</title>
            <link>http://www.medworm.com/index.php?rid=629320&amp;cid=t_121576_134_f&amp;fid=35137&amp;url=http%3A%2F%2Fdiabetesupdate.blogspot.com%2F2007%2F05%2Fdream-study-avandia-kills-people.html</link>
            <description>As reported by the New York Times today. The DREAM study, which Glaxo, the manufacturer of Avandia ran to prove that Avandia would improve the health of people without diabetes so they could sell it to everyone else, instead found this:&quot;...patients taking Avandia had 66 percent more heart attacks, 39 percent more strokes and 20 percent more deaths from cardiovascular-related problems. That outcome, Dr. Nissen [writing in the New England Journal of medicine] wrote, “virtually precludes the possibility of an overall benefit and suggest [sic] an unexpected mechanism for harm.”http://www.nytimes.com/2007/05/22/business/21drug-web.html?hpThere are already quite a few studies showing that Avandia and its evil twin, Actos, don't do much for blood sugar. What they do do, very well, is grow new...</description>
            <author>Diabetes Update</author>
            <type>blogs</type>
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            <pubDate>Mon, 21 May 2007 17:24:00 +0100</pubDate>
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