N-nitrosodimethylamine (NDMA) is a hepatotoxic agent and carcinogen contaminant in commonly used medications such as valsartan, losartan, irbesartan, and ranitidine. NDMA can be produced during manufacture, introduced from contaminated ingredients procured elsewhere, or introduced from contaminated solvents and catalysts. The Food and Drug Administration has established a maximum dose of NDMA that is permissible per tablet and guidance for manufacturers. However, many unanswered questions about NDMA contamination need rigorous investigation.
CITATION STYLE
White, C. M. (2020, June 1). Understanding and Preventing (N-Nitrosodimethylamine) NDMA Contamination of Medications. Annals of Pharmacotherapy. SAGE Publications Inc. https://doi.org/10.1177/1060028019892222
Mendeley helps you to discover research relevant for your work.