Pfizer is voluntarily recalling some lots of its antidepressant Effexor XR because a single capsule of a different medication was found in one bottle of the drug.The recall is for one lot of 30-count ...

The FDA has approved Wyeth’s antidepressant Effexor XR (venlafaxine), the company’s top-selling Rx drug, for the treatment of adults with panic disorder. Effexor XR is the first drug to be approved to ...

NEW YORK (AP) -- Pfizer said Thursday it is recalling some lots of its antidepressant Effexor XR because a single capsule of a different medication was found in one bottle of the drug. Pfizer is ...

Madison, NJ, February 11, 2003 -- Wyeth (NYSE:WYE) announced today that the U.S. Food and Drug Administration (FDA) approved EFFEXOR (R) XR (venlafaxine HCl) for the treatment of patients with social ...

Pfizer has issued a recall for one lot of 30-count Effexor XR (venlafaxine HCl) 150 mg extended-release capsules, one lot of 90-count Effexor XR (venlafaxine HCl) 150 mg extended-release capsules and ...

Nov. 28, 2005 -- The U.S. Food and Drug Administration (FDA) has approved extended-release venlafaxine HCl capsules for the treatment of adults with panic disorder; sodium oxybate oral solution for ...

TORONTO, ON / ACCESSWIRE / November 27, 2018 / Intellipharmaceutics International Inc. (NASDAQ and TSX:IPCI) ("Intellipharmaceutics" or the "Company"), a pharmaceutical company specializing in the ...

Johnson & Johnson’s drug delivery unit Alza has filed a lawsuit against Wyeth, alleging that its top-selling Effexor XR antidepressant infringes one of J&J’s patents covering controlled release ...

The FDA’s Division of Drug Marketing, Advertising, andCommunications says a Wyeth professional journal ad for Effexor XR (venlaxineHCl) tablets was misleading because it overstated the drug’s efficacy ...

Q. I tried to get off Effexor XR (venlafaxine) a few years ago, and the results were typical: agony, muscle aches, “brain zaps” and a depression worse than I had before starting on the drug. Six ...