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Baeshen NA, Baeshen MN, Sheikh A, Bora RS, Ahmed MM, Ramadan HA, et al
Why it was included in the FDA ban The FDA cites significant safety risks due to the potential for congestive heart failure in certain patients seen in a clinical trial that was terminated
Injection-site irritation is possible but uncommon
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Volumes more than 10 ml should be split and given at separate intramuscular or subcutaneous sites
The 12 mg arm started at 2 mg and increased every four weeks through 4 mg, 6 mg, 9 mg, and 12 mg
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