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Proposed FDA Rule Could Limit Pharmacy Compounding By: Ned Milenkovich, PharmD, JD On March 20, 2024, the FDA proposed a new rule that would create criteria for certain drug products or categories that present Demonstrable Difficulties for Compounding Listsknown as DDC lists

However, fatigue can have many causes, so evaluation from a healthcare provider is recommended

Bottom line: For a 10 mg vial of tirzepatide, 1 mL of bacteriostatic water is the standard diluent amount, resulting in a concentration of 1 mg per 10 units on a U-100 syringe

There are several complications that may occur during or after the procedure

283, G1264G1275 (2002)