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European Commission approves statement on lipid improvement for Viramune label
Boehringer Ingelheim, 07/07/09
Boehringer Ingelheim announced today that the European Commission has approved an update of the Summary of Product Characteristics for Viramune in the treatment of patients with HIV. The decision followed a positive recommendation by the Committee for Medical Products for Human Use (CHMP), the scientific committee of the European Medicines Agency (EMEA) who reviewed the clinical evidence and approved a statement in the SmPC recognising the positive effect of nevirapine on the lipid profile of HIV infected patients.
Today in Drug Approvals...keeping you current
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Boston Scientific Announces FDA Clearance and CE Mark for WallFlex Fully Covered Esophageal Stent
Boston Scientific, 11/24/09
Dendreon Receives FDA Acknowledgement of Complete Response
Dendreon Coproration, 11/23/09
ImmunoGen, Inc. Announces Second License Taken by Amgen for Right to Use the Companys TAP Technology
ImmunoGen, Inc., 11/20/09
Today in Drug/Product Alerts...keeping you current
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Generic Anticonvulsant Use in Children: Do We Have Evidence to Recommend Brand Formulations?
Archives of Neurology, 11/23/09
Medtronic Receives FDA Warning Letter Following Inspection of Its Mounds View, Minn. Facility
Medtronic, 11/19/09
Therapy modifications and low-density lipoprotein cholesterol goal attainment rates associated with the initiation of generic simvastatin
Current Medical Research and Opinion, 11/17/09
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