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In all of the clinical trials, semaglutide was administered subcutaneously using a prefilled pen (4 mm, 32-gauge needle) at an initial dose of 0.25 mg/week for the first 4 weeks, followed by a 12-week dose escalation (0.5, 1.0 and 1.7 mg/week each for 4 weeks) up to 2.4 mg/week by the end of week 16, depending on individual tolerance (with 1.7 mg once weekly permitted for those who were not able to reach the 2.4 mg dose, but with at least one attempt to re-escalate to the full 2.4 mg dose)

Never marketed for human use

However, we absolutely stand behind our ingredient and our science. The class action also notes that while studied individually, the extracts as combination supplement have not been tested

This cautious approach can help identify any adverse reactions to new supplements.