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Regulators protecting patients in the news The FDA posted letters warning drug manufacturing companies in Connecticut and Missouri to correct sterility issues in their production of over-the-counter drug products
In a collaborative effort, two designated authors (AM and SS) independently undertook the assessment, with any incongruences resolved through consultation with a senior authority (HR)
Consequently, product labeling for agents such as semaglutide and tirzepatide advises discontinuation at least two months before planned conception to allow for pharmacokinetic clearance
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