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Results from 327 women demonstrated: Significant increases in satisfying sexual events compared to placebo at 1.25 mg and 1.75 mg doses Improved Female Sexual Function Index total scores (mean improvement of 3.6 points vs 1.9 for placebo) Reduced sexual distress as measured by Female Sexual Distress Scale scores Dose-dependent response with optimal effects at 1.75 mg Two Phase 3 trials (RECONNECT studies) enrolled over 1,200 premenopausal women with acquired, generalized HSDD and confirmed efficacy at the 1.75 mg dose administered subcutaneously at least 45 minutes before anticipated sexual activity

Each serving provides 2,000mg, ensuring effectiveness

Factors other than the amount of the implanted material may influence adverse effects after PP prosthetic implantation

Follow the storage conditions on your vial label

The GLP-1 Dominance Gap Is Widening Mounjaro and Zepbound Lillys twin blockbusters targeting diabetes and obesity combined for $11.7 billion in Q4 revenue alone