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.

While there is a very low probability that other bottles of Effexor XR contain a Tikosyn capsule, Pfizer has initiated this voluntary recall as a precaution. This recall is to the patient level ...

Pfizer announced a voluntary recall of venlafaxine HCl after a pharmacist reported that one bottle in the lot being recalled contained one capsule of dofetilide 0.25mg. The recall includes one lot ...

The Food and Drug Administration has approved the first generic version of Effexor XR capsules (venlafaxine hydrochloride) to treat major depressive disorder. Venlafaxine hydrochloride extended ...

To reduce the risk for overdose, the FDA advises that venlafaxine prescriptions be written for the smallest quantity of capsules consistent with good patient management.

A report by a pharmacist claiming to have found one capsule of Tikosyn (dofetilide) in a bottle of Effexor XR (venlafaxine HCl extended-release) capsules has prompted Pfizer to initiate a recall ...

Zydus announced a voluntary recall of Venlafaxine HCl ER 75mg and 150mg Capsules due to an out of specification dissolution result in a retained sample.

Reason for posting: A change in the prescribing information for venlafaxine has been issued by the US manufacturer, based on concerns that the antidepressant drug has been associated, in cases of ...

Had ratiopharm not directed Alembic to stand-down manufacturing, Alembic would have had “probably around 7 million” venlafaxine capsules in inventory.

The FDA has approved new indications for extended-release venlafaxine HCl capsules (Effexor XR) and sodium oxybate oral solution (Xyrem), and a new dosing regimen for micronized fenofibrate ...

Pursuant to the license agreement, Mylan will be granted a non-exclusive license to the relevant patents that would permit Mylan to launch Venlafaxine HCl ER Capsules in the U.S. on or after June ...