|
|
|
|
Pharmaceutical Mistake Leads to Recall of Prominent Antibiotic SCOTTSDALE, Ariz. -Medicis today announced that the Company is voluntarily recalling lot numbers B080037 (Exp: 12/09) and B080038 (Exp: 12/09) of the antibiotic SOLODYNŽ (minocycline HCl, USP) Extended Release Tablets, 90 mg, 30-count bottles (NDC 99207-461-30). Medicis has received a report that one bottle in lot number B080037 contains AZASANŽ (azathioprine tablets) 75 mg (NDC 65649-231-51) instead of SOLODYNŽ (minocycline HCl, USP) Extended Release Tablets, 90 mg. AZASANŽ is an immuno-suppressive agent used in transplant patients to prevent kidney rejection and for the treatment of rheumatoid arthritis. Taking AZASANŽ instead of SOLODYNŽ presents a health hazard and safety risk to patients. Side effects associated with the use of AZASANŽ, particularly in the elderly, include mylosuppression (decrease in the number of red and white blood cells and platelets), infection, bleeding, chills, nausea, vomiting and diarrhea. Joint and muscle pain are also common side effects. Unanticipated interactions with other drugs may also lead to serious adverse events. SOLODYNŽ is manufactured by AAIPharma, Inc. under contract to Medicis. The two lots were manufactured during February 2008. The recall is limited to these lots, and ample supplies of SOLODYNŽ remain on the market. |
|
Thank You to Our Sponsors!
Entire site copyright 2008 by Public Health Alert, |