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Science | AAAS
That infuriated the Solidarity team. "The mantra I've always heard as a joke about the FDA, is that they say ‘In God we trust, everyone else has to provide data,’” Kieny says. “So look at all the data."
Solidarity’s finings, WHO’s chief scientist, Soumya Swaminathan, notes that 50% of the 2750 patients who received remdesivir in the trial were from Canada and Europe, places recognized for high quality health care. And she stresses that the other participating countries do not necessarily have substandard care.
Questions have also arisen about the potential of remdesivir to do harm. WHO has a regular overview of possible adverse drug events related to COVID-19 treatments. In late August it noted a disproportionately high number of reports of liver and kidney problems in patients receiving remdesivir compared with patients receiving other drugs for COVID-19, The European Medicines Agency (EMA) also announced this month that its safety committee had started a review to assess reports of acute kidney injuries in some patients taking remdesivir.

