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        <title>Archives of Drug Information via MedWorm.com</title>
        <description>MedWorm.com provides a medical RSS filtering service. Over 6000 RSS medical sources are combined and output via different filters. This feed contains the latest items from the 'Archives of Drug Information' source.</description>
        <link><![CDATA[http://www.medworm.com/rss/search.php?qu=Archives+of+Drug+Information&t=Archives+of+Drug+Information&s=Search&f=source]]></link>
        <lastBuildDate>Wed, 17 Mar 2010 14:16:56 +0100</lastBuildDate>
        <item>
            <title>Safety and Efficacy in HIV-1-Infected Patients Treated with Ritonavir-Boosted Saquinavir Mesylate</title>
            <link>http://www.medworm.com/index.php?rid=3206080&amp;cid=s_37711_13_f&amp;fid=37711&amp;url=http%3A%2F%2Fdx.doi.org%2F10.1111%252Fj.1753-5174.2009.00028.x</link>
            <description>Objective. To evaluate the safety, tolerability, and efficacy of ritonavir-boosted saquinavir 1000/100 mg twice daily administered as a 500 mg film-coated tablet in HIV-1-infected patients.Methods. In this open-label, observational, 24-week survey conducted in 8 European countries, eligible HIV-infected participants had been prescribed saquinavir/ritonavir in combination with other nonprotease inhibitor (PI) antiretroviral agents as part of their HIV treatment regimen. The safety (grade 3 or 4 adverse events [AEs]), tolerability (by an investigator-reported subjective rating system), and efficacy (the percentage of participants with (Source: Archives of Drug Information)</description>
            <author>Archives of Drug Information</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=3206080</comments>
            <pubDate>Tue, 26 Jan 2010 00:00:00 +0100</pubDate>
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            <title>Effect of 4-Aminopyridine on Action Potential Parameters in Isolated Dog Purkinje Fibers</title>
            <link>http://www.medworm.com/index.php?rid=3090695&amp;cid=s_37711_13_f&amp;fid=37711&amp;url=http%3A%2F%2Fdx.doi.org%2F10.1111%252Fj.1753-5174.2009.00027.x</link>
            <description>Introduction. 4-Aminopyridine (fampridine), a potassium channel blocker, has demonstrated efficacy in improving lower extremity strength and walking speed in patients with multiple sclerosis. Since in vitro electrophysiologic studies are recommended for evaluating a drug's potential to prolong the QT interval and induce such cardiac arrhythmias as Torsades de Pointes, we examined the electrophysiologic effects of 4-aminopyridine (0.5, 5.0, 50, and 500 µM) on isolated canine Purkinje fibers.Methods. Microelectrodes monitored the resting membrane potential, overshoot, amplitude of action potential (AP), and maximal rate of depolarization of the AP upstroke in Purkinje fibers stimulated at 0.5 and 1.0 Hz.Results. None of the above variables were altered in the presence of 4-aminopyridine. Th...</description>
            <author>Archives of Drug Information</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=3090695</comments>
            <pubDate>Wed, 16 Dec 2009 00:00:00 +0100</pubDate>
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            <title>Efficacy and Safety of Efalizumab in Patients with Moderate-to-Severe Plaque Psoriasis Resistant to Previous Anti-Psoriatic Treatment: Results of a Multicentre, Open-label, Phase IIIb/IV Trial</title>
            <link>http://www.medworm.com/index.php?rid=3058136&amp;cid=s_37711_13_f&amp;fid=37711&amp;url=http%3A%2F%2Fdx.doi.org%2F10.1111%252Fj.1753-5174.2009.00026.x</link>
            <description>Conclusions. Efalizumab provided effective control of psoriasis in the majority of patients during the initial treatment period. The high response rates were maintained in initial responders when treatment was continued beyond 12 weeks. (Source: Archives of Drug Information)</description>
            <author>Archives of Drug Information</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=3058136</comments>
            <pubDate>Sat, 05 Dec 2009 00:00:00 +0100</pubDate>
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        <item>
            <title>Efalizumab in the Treatment of Scalp, Palmoplantar and Nail Psoriasis: Results of a 24-Week Latin American Study</title>
            <link>http://www.medworm.com/index.php?rid=3045987&amp;cid=s_37711_13_f&amp;fid=37711&amp;url=http%3A%2F%2Fdx.doi.org%2F10.1111%252Fj.1753-5174.2009.00025.x</link>
            <description>Conclusions. This open-label, uncontrolled study provides supportive evidence of the potential of efalizumab as a treatment for nail, scalp and palmoplantar psoriasis. (Source: Archives of Drug Information)</description>
            <author>Archives of Drug Information</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=3045987</comments>
            <pubDate>Wed, 02 Dec 2009 00:00:00 +0100</pubDate>
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        <item>
            <title>Control of Moderate-to-Severe Plaque Psoriasis with Efalizumab: 24-Week, Open-Label, Phase IIIb/IV Latin American Study Results</title>
            <link>http://www.medworm.com/index.php?rid=3024106&amp;cid=s_37711_13_f&amp;fid=37711&amp;url=http%3A%2F%2Fdx.doi.org%2F10.1111%252Fj.1753-5174.2009.00024.x</link>
            <description>Conclusions. Efalizumab demonstrated sustained control of psoriasis up to 24 weeks in patients from Latin America, confirming results seen in Phase III studies conducted in North America and Europe. (Source: Archives of Drug Information)</description>
            <author>Archives of Drug Information</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=3024106</comments>
            <pubDate>Wed, 25 Nov 2009 00:00:00 +0100</pubDate>
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            <title>Assessing the Impact of Efalizumab on Nail, Scalp and Palmoplantar Psoriasis and on Quality of Life: Results from a Multicentre, Open-label, Phase IIIb/IV Trial</title>
            <link>http://www.medworm.com/index.php?rid=3013978&amp;cid=s_37711_13_f&amp;fid=37711&amp;url=http%3A%2F%2Fdx.doi.org%2F10.1111%252Fj.1753-5174.2009.00023.x</link>
            <description>This post-approval, open-label trial (n = 1266) assessed the efficacy of efalizumab, administered in accordance with the European label at that time, in patients with concomitant nail, scalp or palmoplantar psoriasis. Patients received subcutaneous efalizumab 1.0 mg/kg weekly for up to 20 weeks. By Week 12, an improvement from baseline of 50% or more was observed in 21.4% (181/844) of patients with nail psoriasis, 62.4% (718/1150) of patients with scalp psoriasis, and 51.4% (127/247) of patients with palmoplantar psoriasis. Quality of life improved throughout the trial, with a 50% median improvement in DLQI score after 12 weeks of treatment. Efalizumab showed promising efficacy in the treatment of nail, scalp and palmoplantar psoriasis, which was reflected in improvements in quality of lif...</description>
            <author>Archives of Drug Information</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=3013978</comments>
            <pubDate>Sat, 21 Nov 2009 00:00:00 +0100</pubDate>
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            <title>Ascorbic Acid Potentiation of Arsenic Trioxide Anticancer Activity Against Acute Promyelocytic Leukemia</title>
            <link>http://www.medworm.com/index.php?rid=2960847&amp;cid=s_37711_13_f&amp;fid=37711&amp;url=http%3A%2F%2Fdx.doi.org%2F10.1111%252Fj.1753-5174.2009.00022.x</link>
            <description>Conclusions. These suggest that AA may enhance the cytotoxicity of As2O3, suggesting a possible future role of AA/As2O3 combination therapy in patients with APL. (Source: Archives of Drug Information)</description>
            <author>Archives of Drug Information</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=2960847</comments>
            <pubDate>Thu, 05 Nov 2009 00:00:00 +0100</pubDate>
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            <title>Effects of 4-Aminopyridine on Cloned hERG Channels Expressed in Mammalian Cells</title>
            <link>http://www.medworm.com/index.php?rid=2735684&amp;cid=s_37711_13_f&amp;fid=37711&amp;url=http%3A%2F%2Fdx.doi.org%2F10.1111%252Fj.1753-5174.2009.00021.x</link>
            <description>Discussion. We observed concentration-dependent inhibition of hERG current with 4-aminopyridine doses between 0.3 and 30 mM. The concentration of 3.8 mM resulting in 50% inhibition (IC50) is approximately three orders of magnitude higher than expected therapeutic plasma concentrations, suggesting 4-aminopyridine has low potential for prolonging QT interval or inducing TdP. (Source: Archives of Drug Information)</description>
            <author>Archives of Drug Information</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=2735684</comments>
            <pubDate>Wed, 26 Aug 2009 23:00:00 +0100</pubDate>
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        <item>
            <title>Change in mRNA Expression after Atenolol, a Beta-adrenergic Receptor Antagonist and Association with Pharmacological Response</title>
            <link>http://www.medworm.com/index.php?rid=2617975&amp;cid=s_37711_13_f&amp;fid=37711&amp;url=http%3A%2F%2Fdx.doi.org%2F10.1111%252Fj.1753-5174.2009.00020.x</link>
            <description>Conclusion. The expression of several genes not previously identified as part of the adrenergic signaling pathway changed in response to a single oral dose of atenolol. Variation in these genes could contribute to unexplained differences in response to [beta]-blockers. (Source: Archives of Drug Information)</description>
            <author>Archives of Drug Information</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=2617975</comments>
            <pubDate>Mon, 20 Jul 2009 23:00:00 +0100</pubDate>
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        <item>
            <title>Drugs Used in the Treatment of Rheumatoid Arthritis: Relationship between Current Use and Cardiovascular Risk Factors</title>
            <link>http://www.medworm.com/index.php?rid=2407465&amp;cid=s_37711_13_f&amp;fid=37711&amp;url=http%3A%2F%2Fdx.doi.org%2F10.1111%252Fj.1753-5174.2009.00019.x</link>
            <description>Conclusions. In a cross-sectional setting drugs used to treat RA did not have major adverse effects on cardiovascular risk factors and use of antimalarials was associated with beneficial lipid profiles. (Source: Archives of Drug Information)</description>
            <author>Archives of Drug Information</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=2407465</comments>
            <pubDate>Fri, 15 May 2009 04:00:00 +0100</pubDate>
            <guid isPermaLink="false">2407465</guid>        </item>
        <item>
            <title>Improved Glycaemic Control with Biphasic Insulin Aspart 30 in Type 2 Diabetes Patients Failing Oral Antidiabetic Drugs: PRESENT Study Results</title>
            <link>http://www.medworm.com/index.php?rid=2407466&amp;cid=s_37711_13_f&amp;fid=37711&amp;url=http%3A%2F%2Fdx.doi.org%2F10.1111%252Fj.1753-5174.2008.00015.x</link>
            <description>Conclusions. BIAsp 30 treatment in a clinical setting improved glycaemic control in type 2 diabetes patients failing OADs. (Source: Archives of Drug Information)</description>
            <author>Archives of Drug Information</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=2407466</comments>
            <pubDate>Wed, 13 May 2009 04:00:00 +0100</pubDate>
            <guid isPermaLink="false">2407466</guid>        </item>
        <item>
            <title>Desloratadine for the Relief of Nasal and Non-nasal Allergy Symptoms: An Observational Study</title>
            <link>http://www.medworm.com/index.php?rid=2269458&amp;cid=s_37711_13_f&amp;fid=37711&amp;url=http%3A%2F%2Fdx.doi.org%2F10.1111%252Fj.1753-5174.2009.00018.x</link>
            <description>Conclusions. In an open-label, uncontrolled, non-randomized, observational study allergy symptoms improved significantly in subjects treated with desloratadine. (Source: Archives of Drug Information)</description>
            <author>Archives of Drug Information</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=2269458</comments>
            <pubDate>Tue, 17 Mar 2009 04:00:00 +0100</pubDate>
            <guid isPermaLink="false">2269458</guid>        </item>
        <item>
            <title>Potential Hepatotoxicity of Efavirenz and Saquinavir/Ritonavir Coadministration in Healthy Volunteers</title>
            <link>http://www.medworm.com/index.php?rid=2218064&amp;cid=s_37711_13_f&amp;fid=37711&amp;url=http%3A%2F%2Fdx.doi.org%2F10.1111%252Fj.1753-5174.2009.00016.x</link>
            <description>Conclusions. The early termination of this study precluded drawing any definitive conclusions regarding the pharmacokinetics at steady state of coadministered saquinavir/ritonavir and efavirenz. (Source: Archives of Drug Information)</description>
            <author>Archives of Drug Information</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=2218064</comments>
            <pubDate>Fri, 27 Feb 2009 05:00:00 +0100</pubDate>
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        <item>
            <title>Utility of Pretreatment Bilirubin Level and UGT1A1 Polymorphisms in Multivariate Predictive Models of Neutropenia Associated with Irinotecan Treatment in Previously Untreated Patients with Colorectal Cancer</title>
            <link>http://www.medworm.com/index.php?rid=1848520&amp;cid=s_37711_13_f&amp;fid=37711&amp;url=http%3A%2F%2Fdx.doi.org%2F10.1111%252Fj.1753-5174.2008.00014.x</link>
            <description>Conclusions. Ability of UGT1A1 or baseline bilirubin to predict neutropenia is low and depends on regimen. (Source: Archives of Drug Information)</description>
            <author>Archives of Drug Information</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=1848520</comments>
            <pubDate>Fri, 03 Oct 2008 04:00:00 +0100</pubDate>
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        <item>
            <title>A Phase 3, Randomized, Placebo-controlled Trial of Filgrastim in Patients with Haematological Malignancies Undergoing Matched-related Allogeneic Bone Marrow Transplantation</title>
            <link>http://www.medworm.com/index.php?rid=1755708&amp;cid=s_37711_13_f&amp;fid=37711&amp;url=http%3A%2F%2Fdx.doi.org%2F10.1111%252Fj.1753-5174.2008.00013.x</link>
            <description>Introduction. Recombinant granulocyte colony-stimulating factor (G-CSF) may aid engraftment post high-dose chemo-/radiotherapy in patients with haematological malignancies undergoing allogeneic bone marrow transplantation (BMT); however, the effects of G-CSF on graft-versus-host disease (GvHD), relapse, and survival are not well defined.Methods. In this double-blind, randomized, placebo-controlled, multicentre, phase 3 study, the effects of the G-CSF Filgrastim on neutrophil and platelet recovery, and on clinical outcomes were evaluated. Patients (12[ndash]55 years) receiving an allogeneic BMT for a haematological malignancy were randomized to receive Filgrastim 5 µg/kg or placebo. Study treatment was continued until patients achieved an absolute neutrophil count (ANC) [ge]0.5 × 109/L, o...</description>
            <author>Archives of Drug Information</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=1755708</comments>
            <pubDate>Wed, 03 Sep 2008 04:00:00 +0100</pubDate>
            <guid isPermaLink="false">1755708</guid>        </item>
        <item>
            <title>Exploratory Study of Tegaserod for Dyspepsia in Women Receiving PPIs for Heartburn</title>
            <link>http://www.medworm.com/index.php?rid=1740082&amp;cid=s_37711_13_f&amp;fid=37711&amp;url=http%3A%2F%2Fdx.doi.org%2F10.1111%252Fj.1753-5174.2008.00012.x</link>
            <description>Conclusions. A significant treatment effect was not demonstrated in this study using a treatment-withdrawal methodology. In future studies of functional dyspepsia patients with heartburn, a more rigorous parallel-group study design should be considered. (Source: Archives of Drug Information)</description>
            <author>Archives of Drug Information</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=1740082</comments>
            <pubDate>Thu, 28 Aug 2008 04:00:00 +0100</pubDate>
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            <title>Patients' Perceptions of Physician-Patient Discussions and Adverse Events with Cancer Therapy</title>
            <link>http://www.medworm.com/index.php?rid=1649756&amp;cid=s_37711_13_f&amp;fid=37711&amp;url=http%3A%2F%2Fdx.doi.org%2F10.1111%252Fj.1753-5174.2008.00011.x</link>
            <description>Conclusions. These findings suggest that discussions alone do not provide patients with sufficient understanding of the events, nor do they appear to adequately equip patients to cope with them. Therefore, efforts to improve cancer care should focus on developing tools to improve patients' understanding of the toxicities of chemotherapy, as well as providing resources to reduce the effects of adverse events. (Source: Archives of Drug Information)</description>
            <author>Archives of Drug Information</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=1649756</comments>
            <pubDate>Thu, 24 Jul 2008 04:00:00 +0100</pubDate>
            <guid isPermaLink="false">1649756</guid>        </item>
        <item>
            <title>Dose Proportionality of Fentanyl Buccal Tablet in Healthy Japanese Volunteers</title>
            <link>http://www.medworm.com/index.php?rid=1609326&amp;cid=s_37711_13_f&amp;fid=37711&amp;url=http%3A%2F%2Fdx.doi.org%2F10.1111%252Fj.1753-5174.2008.00007.x</link>
            <description>Conclusions. Systemic exposure to FBT was approximately dose proportional across the range 100 µg to 800 µg in healthy Japanese adults. Adverse events were mild or moderate. (Source: Archives of Drug Information)</description>
            <author>Archives of Drug Information</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=1609326</comments>
            <pubDate>Fri, 11 Jul 2008 04:00:00 +0100</pubDate>
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            <title>Impact of Desloratadine on Symptoms and Quality of Life in Subjects with Chronic Idiopathic Urticaria: A Multicenter, Practice-based Study</title>
            <link>http://www.medworm.com/index.php?rid=1609329&amp;cid=s_37711_13_f&amp;fid=37711&amp;url=http%3A%2F%2Fdx.doi.org%2F10.1111%252Fj.1753-5174.2008.00010.x</link>
            <description>Conclusion. In an open-label, observational study, desloratadine 5 mg once daily significantly decreased symptoms of chronic idiopathic urticaria and improved subject QoL. (Source: Archives of Drug Information)</description>
            <author>Archives of Drug Information</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=1609329</comments>
            <pubDate>Tue, 08 Jul 2008 04:00:00 +0100</pubDate>
            <guid isPermaLink="false">1609329</guid>        </item>
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            <title>Relative Bioavailability of Fentanyl Following Various Dosing Regimens of Fentanyl Buccal Tablet in Healthy Japanese Volunteers</title>
            <link>http://www.medworm.com/index.php?rid=1609328&amp;cid=s_37711_13_f&amp;fid=37711&amp;url=http%3A%2F%2Fdx.doi.org%2F10.1111%252Fj.1753-5174.2008.00009.x</link>
            <description>Conclusions. Bioavailability of fentanyl after FBT 400 µg administered as a single tablet was bioequivalent to that after 2 simultaneously administered 200 µg tablets in healthy Japanese volunteers. AEs were mild or moderate. (Source: Archives of Drug Information)</description>
            <author>Archives of Drug Information</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=1609328</comments>
            <pubDate>Sat, 28 Jun 2008 04:00:00 +0100</pubDate>
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            <title>Extent of Fentanyl Accumulation Following Multiple Doses of Fentanyl Buccal Tablet 400&amp;nbsp;&amp;micro;g in Healthy Japanese Volunteers</title>
            <link>http://www.medworm.com/index.php?rid=1609327&amp;cid=s_37711_13_f&amp;fid=37711&amp;url=http%3A%2F%2Fdx.doi.org%2F10.1111%252Fj.1753-5174.2008.00008.x</link>
            <description>Conclusions. Following administration of FBT at 6-hour intervals to healthy Japanese volunteers, at steady state, fentanyl exposure was higher by 55% (AUC0[ndash]6) and 23% (Cmax) than after a single dose of FBT. Adverse events were mild or moderate. (Source: Archives of Drug Information)</description>
            <author>Archives of Drug Information</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=1609327</comments>
            <pubDate>Sat, 28 Jun 2008 04:00:00 +0100</pubDate>
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