A report by a pharmacist claiming to have found one capsule of the antiarrhythmic agent Tikosyn (dofetilide) in a bottle of Effexor XR (venlafaxine HCl extended-release capsules) has prompted Pfizer ...
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 ...
On June 28, the U.S. Food and Drug Administration approved the first generic version of Effexor XR capsules (venlafaxine hydrochloride) to treat major depressive disorder. Venlafaxine hydrochloride ...
I won't rehash the reason because I'd just get angry all over again. I'm taking 2 75mg capsules of Effexor XR (extended release) instead of my normal 150mg capsules. My daily doseage is 450mg so that ...
Pfizer Initiates Nationwide Voluntary Recall of Two Lots of Pfizer's Effexor XR® 150 Mg Extended-Release Capsules and One Lot of Greenstone's Venlafaxine HCl 150 Mg Extended-Release Capsules Due to ...
Effexor XR (venlafaxine) is a prescription drug used to treat depression, panic disorder, and certain types of anxiety. It comes as an extended-release oral capsule. (Extended-release capsules slowly ...
Cymbalta is approved for children 7 years and older, but Effexor XR is only for adults. Both Cymbalta and Effexor XR have a ...
Pharmaceutical and biotechnology major Wockhardt has received final approval from the United States Food & Drug Administration (US FDA) for marketing 37.5mg, 75mg and 150mg extended release capsules ...
Effexor XR (venlafaxine) is a prescription drug used to treat certain mental health conditions, such as major depressive disorder. The drug has a boxed warning for an increased risk of suicidal ...
We were unable to process your request. Please try again later. If you continue to have this issue please contact customerservice@slackinc.com. Pfizer announced a voluntary recall of venlafaxine HCl ...
Pharmaceutical and biotechnology major Wockhardt has received final approval from the United States Food & Drug Administration (US FDA) for marketing 37.5mg, 75mg and 150mg extended release capsules ...