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On March 10 th , the FDA issued guidance clarifying that 503A and 503B drug compounders must soon cease compounding semaglutide injection products[i] or risk enforcement action.[ii] This has a significant impact on compounding pharmacies as, under the Federal Food, Drug, and Cosmetic Act (the FD&C ), drug compounders are permitted to compound their own copies of a patented drug if the FDA determines it is in shortage

from day 2028 they were treated with the nephrotoxic drug gentamicin (85 mgkgbmday 1 )

The primary allegation against Roundup is that its active ingredient, glyphosate, is carcinogenic and may lead to the development of certain types of cancer, particularly non-Hodgkins lymphoma