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After the initial trial, participants were randomly assigned to either an LC group (2 g twice daily for 7 days) or a placebo group, consuming citrus drinks
However, plaintiffs allege that the risks of severe outcomes were not adequately disclosed at the time they were prescribed the medication
Future research could focus on the detailed physiological processes involved in these side effects
Legal status (US): Tesamorelin is FDA-approved under the brand names Egrifta and Egrifta WR, manufactured by Theratechnologies, specifically to reduce excess visceral abdominal fat in HIV-infected patients with lipodystrophy
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