On June 8, 2011, the United State's Food and Drug Administration (FDA) released new warnings about the dangers of high-dose simvastatin, which affects many people. The FDA also issued new warnings about its dosing and drug interactions. This article calls our attention to this FDA's warning.
Simvastatin, a popular statin, is a generic. It is quite popular and on all the pharmacy plans. Besides, the price point is right and prescribing is hassle free. In 2010, an estimated 2.1 million patients, in the US alone, were prescribed a product containing 80 mg simvastatin. Can you imagine how many would have been on it worldwide?
The highlights of the warnings:
Restrictions for 80-mg simvastatin
- Avoid prescribing 80-mg simvastatin because of the high risk for myopathy.
- 80-mg simvastatin is satisfactory if the patient has been on it for a year with no evidence of myopathy.
- No more than 20 mg for patients taking amlodipine and ranolazine
- No more than 10 mg for patients on amiodarone, verapamil, and diltiazem
- The FDA has mandated drug-labeling changes warning that simvastatin is contraindicated in patients on gemfibrozil, certain antifungal medications (itraconazole, ketoconazole, posaconazole), certain antibiotics (erythromycin, clarithromycin, telithromycin) as well as HIV protease inhibitors, nefazodone, cyclosporine, and danazol.
So why didn't the FDA act sooner? That's not clear, but the word is out now.
Simvastatin problems are public property. Patients know about them and depend on doctors to clear up their medication regimens. Not all statins are created equal and the least expensive drug may not necessarily be the best for your patient.
Source:
The above article is reproduced from material entitled 'Clarifying Simvastatin Warnings -- It's Not Just 80 mg' by Medscape Internal Medicine. Retrieved 5.10.2011 from here. Note: Materials may be edited for content and length.
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