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Because of both the potential for HIV-1 infection transmission and serious adverse reactions in nursing infants, mothers receiving tesamorelin should be instructed not to human milk-feed
Adverse Reactions in Seven Pooled 12-Week Controlled Trials In seven pooled 12-week, double-blind, randomized, placebo-controlled trials, 993 patients received 140 mg of REPATHA subcutaneously every 2 weeks and 1059 patients received 420 mg of REPATHA subcutaneously monthly
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