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MEN 2 is a hereditary syndrome characterized by MTC, pheochromocytoma, and parathyroid abnormalities, caused by mutations in the RET proto-oncogene

Pediatr Res 19 : 13181321 Fink JK, Brouwers P, Barton N, Malekzadeh MH, Sato S, Hill S, Cohen WE, Fivush B, Gahl WA 1989 Neurologic complications in long-standing nephropathic cystinosis

While they are not FDA-approved in the same way branded drugs are, they are a common alternative used by providers to meet specific patient needs or address medication shortages

(2024) Gastroenterology n=1094 Comprehensive safety analysis of retatrutide trials examining amylase, lipase, calcitonin, pancreatic imaging, and pancreatitis incidence across 72-week treatment duration