EMA calcitonin alert

July 23, 2012

THE European Medicines Agency has ordered the withdrawal of intranasal formulations of calcitonin for treatment of osteoporosis, because of evidence that long-term use of the medicines is associated with an increased risk of developing cancer. Henceforth calcitonin will only be available as a solution for injection and infusion in Europe, indicated for prevention of acute bone loss due to sudden immobilisation, with a max four week treatment duration. It can also be used for Paget’s disease in patients who do not respond to alternative treatments, or hypercalcaemia due to cancer. “Treatment with calcitonin should be limited to the shortest possible time and using the minimum effective dose,” the EMA said.

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Pharmacy Daily | EMA calcitonin alert

EMA calcitonin alert

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