FDA approval Risedronate – Actonel clinical trails
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FDA approval for Risedronate – Actonel

The US Food and Drug Administration (FDA) approved Risedronate for treatment and prevention of Paget’s disease in 1998 and the prevention and treatment of osteoporosis in 1999. FDA has given its approval to a brand new four month dose of 150mg of Actonel for treatment prevention of post menopausal osteoporosis. Risedronate is approved as a drug for women who have entered the menopausal phase of their life.

The drug has shown positive results for bringing down the number of fractures in women who are facing both menopause and osteoporosis. The effectiveness of the once a month dose and the regular daily dose was checked and the results were found to be similar. The BMD or bone mineral density had the same amount of hike in patients taking the daily dose and those taking the once a month dose.

More than 55 million prescriptions of for this drug have been given to the patients in the United States of America itself. The manufacturer of this pill is confident that it is the future solution to all bone related problems. They are so confident as the results of the clinical trials are very encouraging. The ever increasing sale of Actonel is another reason why the manufacturer is so confident.

Osteoporosis is such a big problem especially for those in the old age. The solution to this problem is to go for a knee replacement surgery but that will be too expensive and the only solution available then is to consult a doctor and start your course of Actonel. This drug has slowed down the bone depletion process and increases the production of calcium in your bones, which makes life easier for you. Women who are in their late forties and early fifties start to develop this problem but now you need not worry. All you have to do is take Actonel and wait for age to catch up with you.
 

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