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Step 2: Calculate and Administer the Starting Dose 6090 Minutes Before the Assessment Window The therapeutic starting dose for libido studies is 0.5mg , administered subcutaneously 6090 minutes before the planned assessment window

When to talk to your provider Contact your provider if you experience no appetite suppression after 4 weeks of consistent use, if side effects worsen rather than improve over time, if you develop mouth sores or persistent oral irritation, or if your results plateau significantly after previously good progress

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Because BPC-157 is not FDA-approved, it's often sold as a research chemical and not all vendors maintain pharmaceutical-grade quality