FDA on Actos

September 21, 2010

THE US Food and Drug Administration has initiated a safety review of the type 2 diabetes drug pioglitazone (Actos). The review comes on the back of concerns raised after an oservational study found that longterm patients on high doses of pioglitazone had an increased risk of developing bladder cancer. At present the FDA is recommending health practitioners continue to follow the label directions when prescribing the drug.

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Pharmacy DailyPharmacy Daily | FDA on Actos

FDA on Actos

Other recent headlines

Prescribing endorsement consultation opens

Call for embedded rural pharmacist pilot

MTick: Behind the menopause ‘one-stop shop’

SEARCH PHARMACY DAILY

Featured video

Recent issues

INDUSTRY JOB VACANCIES