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Description
The FDAs adverse event reporting system, or FAERS database, is designed to support the FDAs post-marketing safety surveillance program for drug and therapeutic biologic products
The standard dose is 37.5 mg once daily, taken in the morning before breakfast or 1 to 2 hours after breakfast
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That changes the M&A landscape for adjacent assets across orthopedics, sleep medicine, cardiology, and diabetes
A thorough history identifies diet changes, exercise patterns, and concurrent medications (diuretics, statins) that could independently cause cramps
