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The FDA label advises that "the developmental and health benefits of breastfeeding should be considered along with the mother's clinical need for tirzepatide and any potential adverse effects on the breastfed infant from tirzepatide or from the underlying maternal condition." This guidance places decision-making responsibility on the healthcare provider and patient, requiring individualized risk-benefit assessment

SURMOUNT-2 ket efficacy results, source: reference [2] Additionally, 81.6% (10 mg) and 86.4% (15 mg) of people taking tirzepatide achieved at least 5% body weight reduction , the other co-primary endpoint, compared to 30.5% of those taking placebo

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Steady-state concentrations are typically achieved after 4 weeks of administration

Does the amount of bacteriostatic water I used during reconstitution change what 60 units delivers
