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  2. Nitrosamine - Wikipedia

    en.wikipedia.org/wiki/Nitrosamine

    The US Food and Drug Administration published guidance about the control of nitrosamine impurities in medicines. [32] [33] Health Canada published guidance about nitrosamine impurities in medications [34] and a list of established acceptable intake limits of nitrosamine impurities in medications. [35]

  3. N-Nitrosodimethylamine - Wikipedia

    en.wikipedia.org/wiki/N-Nitrosodimethylamine

    Generally, people should not be exposed to a lifetime risk of cancer exceeding 1 in 100,000 from nitrosamines in their medicines. [12] EU regulators first became aware of nitrosamines in medicines in mid-2018, and took regulatory actions, including recalling medicines and stopping the use of active substances from certain manufacturers. [ 12 ]

  4. Nitrosamine impurities may increase the risk of cancer if people are exposed to them above acceptable levels and over long periods of time,” the agency adds, “but a person taking a drug ...

  5. Rifapentine - Wikipedia

    en.wikipedia.org/wiki/Rifapentine

    In August 2020, the U.S. Food and Drug Administration (FDA) became aware of nitrosamine impurities in certain samples of rifapentine. [11] The FDA and manufacturers are investigating the origin of these impurities in rifapentine, and the agency is developing testing methods for regulators and industry to detect the 1-cyclopentyl-4 ...

  6. N-Nitrosamides - Wikipedia

    en.wikipedia.org/wiki/N-Nitrosamides

    An alternative possible formation of diazonium and carbenium ions is through the enzymatic reaction of nitrosamines. [ 5 ] Typical accompanying symptoms during the medical cancer treatment via N -nitroso ureas are the impairment of bone marrow (damage of the stem cell compartment), lymphatic tissue and the gastrointestinal tract.

  7. Nitrosamine formation during digestion - Wikipedia

    en.wikipedia.org/wiki/Nitrosamine_formation...

    The effects of nitroso compounds vary dramatically across the gastrointestinal tract, and with diet. Nitroso compounds present in stool do not induce nitrosamine formation, because stool has neutral pH. [7] [8] Stomach acid catalyzes nitrosamine compound formation and is the main location of the reaction during digestion. [9]

  8. Tobacco-specific nitrosamines - Wikipedia

    en.wikipedia.org/wiki/Tobacco-specific_nitrosamines

    Among the tobacco-specific nitrosamines, nicotine-derived nitrosamine ketone (NNK) and N-nitrosonornicotine (NNN) are the most carcinogenic. [1] Others include N ′-nitrosoanatabine (NAT) and N-nitrosoanabasine (NAB). NNK and its metabolite 4-(methylnitrosamino)-1-(3-pyridyl)-1-butanol (NNAL) are potent systemic lung carcinogens in rats ...

  9. N-Nitrosoglyphosate - Wikipedia

    en.wikipedia.org/wiki/N-Nitrosoglyphosate

    N-Nitrosoglyphosate is the nitrosamine degradation product and synthetic impurity of glyphosate herbicide. The US EPA limits N-nitrosoglyphosate impurity to a maximum of 1 ppm in glyphosate formulated products. [1] N-Nitrosoglyphosate can also form from the reaction of nitrates and glyphosate.