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An American court is biased at the pharmaceutical companies in the Zantak case and excludes cancer evidence

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Friday 11/July/2025 – 08:11 PM

















The Supreme Court in the American state of Dilayer ruled that the certificates submitted by medical experts and scientists in a collective case lifted about 75,000 patients against 4 of the major pharmaceutical companies, accusing her that the adulterers to treat heartburn caused their cancer.

Dilayer Supreme Court is biased to pharmaceutical companies in the Zantak case and excludes cancer evidence

According to Rouz, the decision was unanimously, and he supported the exclusion of the testimonies of ten medical experts, who had indicated that the active substance in Zantak, Ranteidine, is linked to an increase in the risk of developing ten different types of cancer, and the companies concerned included: Glaxo Smith Klein, Phazer, Sanovi, and Bohringer Angelicheim.

Judge Abjejo explained that the first -class court committed a legal error using a criterion for a lenient in evaluating the testimonies of experts, as it was not obligated to provide a reliable scientific methodology that supports their conclusions.

She pointed out that the original judge failed to play her role as a gatekeeper to assess the credibility of scientific certificates.

This step comes after a previous decision issued by the US Food and Drug Administration in April 2020 to withdraw the Zantak medicine from the market, as a result of fears of the decomposition of Ranitidine to the NDMA compound known for its carcinogenic properties, especially when exposed to heat or the passage of time.

Lawyer Brent Wizner, the legal actor of patients, said that they still have a strong scientific record that supports their allegations, and will rush to prepare for a possible trial despite the judicial decision.

For its part, pharmaceutical companies have repeatedly confirmed that there is no reliable scientific evidence linking Zantac to cancer or that patients were exposed to dangerous levels of NDMA when using the drug.



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