Pfizer Recalls Batch of Antidepressant Due to Contamination
Three lots of venlaxafine have just been recalled because one bottle contained one pill of a heart drug that could kill a person who didn't need it. The heart drug was an anti-arrhythmic called dofetilide/Tikosyn that could cause your heart to go wonky. The irony strikes me because there is always such noise about Quality Assurance for supplements and herbal medicines. Do people really believe that anything manufactured and packaged by Big Pharm is assuredly Safe? Another thing that strikes me as insane is the fact that brand names of pharmaceuticals are Capitalized. Who decided on That??
Recalled products: 30-count Effexor XR (venlafaxine HCI) 150 mg extended-release capsules 90-count Effexor XR (venlafaxine HCl) 150 mg extended-release capsules Effexor lot numbers V130142 and V130140, exp October 2015 90-count Greenstone LLC-branded venlafaxine HCl 150 mg extended-release capsules Greenstone lot number V130014, exp August 2015.
Potentially faulty product should be returned to Stericycle Inc, 1-888-345-0481. Questions go to Pfizer Medical Information at 1-800-438-1985 Adverse reactions should be reported to www.fda.gov/medwatch/report.htm.