The FDA can save lives by adding new warning labels
May 1, 2017. There's evidence that Paxil raises the risk of suicidal behavior in adults, yet that's not on the warning label. The new FDA commissioner could. PAXIL paroxetine hydrochloride is an orally administered psychotropic drug. It is the. thioridazine is contraindicated see WARNINGS and PRECAUTIONS. Apr 2, 2014. The FDA posted the warning letter to its website Tuesday citing a GSK $GSK plant in Cork, Ireland, following a 5-day inspection last October.
GSK recalls Paxil after FDA issues
Dec 8, 2005. At the FDA's request, the manufacturer has changed paroxetine's pregnancy. to the Warnings section of paroxetine's prescribing information. Read the Medication Guide that comes with PAXIL before you start taking it and. PAXIL and other antidepressant medicines may cause serious side effects.
Paroxetine - Wikipedia
Paroxetine, also known by the trade names Paxil and Seroxat among others, is an. The FDA conducted a statistical analysis of paroxetine clinical trials in. the U. S. FDA published a warning regarding "severe" discontinuation symptoms. Understanding how inclusion of specific health information in FDA warnings. Did the use of paroxetine either generic or under brand name Paxil decline after.