Topic: GlaxoSmithKline plc

Drug and medical device firm Abbott Laboratories said Friday it has abandoned plans to sell its vaccines unit, less than three months after ...
Use of acetaminophen in children may increase the risk of asthma, eczema, and rhinoconjunctivitis, according to research published online Aug. 13...
Part IV in a series on Medicine's Suicide Problem. Part I is HERE, Part II is HERE, and part III is HERE.). . Psychiatrist Arif Khan has spent...
A collection of medical articles from around the Web:. The New York Times' Donald G. McNeil, Jr., takes a look at the science behind the tiny ...
GlaxoSmithKline (NYSE: GSK) and Valeant Pharmaceuticals International (NYSE: VRX) announced the U.S. Food and Drug Administration (FDA) has ...

FDA delays review of Glaxo epilepsy drug

The U.S. Food and Drug Administration has pushed back the review date for GlaxoSmithKline's new epilepsy treatment.. . The FDA now says it will ...
European Medicines Agency investigates if there's a link between swine flu shot, narcolepsyThe European Medicines Agency is investigating whether there is a link between narcolepsy and a swine flu vaccine.Narcolepsy is a rare disorder that causes people t

EU drugs regulator reviews safety of GSK's flu jab

LONDON (Reuters) - Europe's drug regulator is reviewing the safety of GlaxoSmithKline's Pandemrix flu vaccine, which has been given to more than 30 million people in Europe, to investigate possible links to a sleep disorder.The European Medicines Agency s

Corrected -Glaxo starts final clinical trial of shingles vaccine

Corrects name of virus in 5th paragraph.LONDON (Reuters) - British pharmaceutical giant GlaxoSmithKline said on Monday it had started final trials of its new vaccine to prevent shingles, one of the most significant products in its pipeline.More than 30,00
FDA panel of advisers backs GlaxoSmithKline seizure drug, despite side effectsFederal health advisers have ruled that GlaxoSmithKline's epilepsy drug Potiga effectively controls seizures.An agency spokeswoman said Wednesday the Food and Drug Administratio