Understanding and Preventing ( N -Nitrosodimethylamine) NDMA Contamination of Medications
Author(s) -
White C. Michael
Publication year - 2020
Publication title -
annals of pharmacotherapy
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.926
H-Index - 113
eISSN - 1542-6270
pISSN - 1060-0280
DOI - 10.1177/1060028019892222
Subject(s) - n nitrosodimethylamine , medicine , contamination , ranitidine , carcinogen , food and drug administration , drug , losartan , pharmacology , toxicology , organic chemistry , chemistry , ecology , angiotensin ii , blood pressure , biology
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.
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