Friday Jul 11
India's Sun Pharma recalls over 40,000 bottles of antidepressant
India's Sun Pharmaceutical Industries Ltd is recalling 41,127 bottles of antidepressant venlafaxine hydrochloride in the United States after the drug failed to dissolve properly, the U.S. Food and Drug Administration said.
Thu Jul 10, 2014
Sun Pharma recalls antidepressant drug from US market
According to a notification by the FDA, the recall of 26,530 units of 30-count bottles and 14,597 units of 90-count bottles is voluntarily initiated by the company through a letter to the regulator last month under 'Class-II' classification.
Mon Jul 07, 2014
venlafaxine, Effexor; Effexor XR
Dr. Charles "Pat" Davis, MD, PhD, is a board certified Emergency Medicine doctor who currently practices as a consultant and staff member for hospitals.
Wed Jun 25, 2014
New study results demonstrate Brintellix (vortioxetine) is...
Valby, 2014-06-26 06:00 CEST -- H. Lundbeck A/S announced results of the SOLUTION trial conducted in Asian patients suffering from Major Depressive Disorder , more commonly referred to as depression.
Placebo for depression: we need to improve the quality of scientific...
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