Nitrosamine contamination withdrawals spread to new drugs

An image showing a photo illustration of a Zantac box and drug tablets

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After ranitidine recalls, EU regulators instruct companies to review all their products for potential impurities

Drugmakers and regulators around the world are mobilising in response to new discoveries of products containing probable carcinogen N-nitrosodimethylamine (NDMA). In particular the European Medicines Agency (EMA) now says that companies should check all their drugs for this and other nitrosamines.

Mona Abdel-Tawab, deputy scientific manager of the Central Laboratory of German Pharmacists welcomes the decision. ‘It’s really high time to initiate such a review on the NDMA content in all drugs,’ she tells Chemistry World. ‘The probability is very high that we are dealing here with a much more general problem than simply the contamination of individual drugs or compounds.’