EMA probes zolpidem

July 15, 2013

THE European Medicines Agency has confirmed a review of insomnia medication zolpidem (Stilnox). The EMA Pharmacovigilance Risk Assessment Committee said it’s reacting to “concerns that some patients may experience drowsiness and slower reactions the day after taking the medicine which could increase the risk of accidents during activities that require alertness, such as driving”. The review follows a Drug Safety Communication issued earlier this year by the US Food and Drug Administration, lowering the recommended dose to 5mg for women and 5-10mg for men.

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Pharmacy Daily | EMA probes zolpidem

EMA probes zolpidem

Other recent headlines

WA group stocks vapes

Fujitsu to protect against cyber threats

PD breaking news – Queensland pharmacies scope of practice pilot expanded

SEARCH PHARMACY DAILY

Featured video

Recent issues

INDUSTRY JOB VACANCIES