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FDA panel rejects Pfizer's arthritis drug as too risky

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U.S. health advisers sharply criticized an experimental arthritis drug Thursday, saying that it was too risky, even with limits on its use.

The expert panel for the Food and Drug Administration voted 19-1 that the drug's modest benefits don’t outweigh its considerable risks, even with proposed measures to restrict who gets the medicine.

Pfizer is seeking FDA approval of the drug, called tanezumab, to treat pain from mild to moderate arthritis in the hips and knees.

It is given by injection every two months. In studies, a small percentage of participants saw their joint damage get worse faster, sometimes requiring hip or knee replacements.

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COVID-19
United States
United States
Cases: 46 252 513
Deaths: 750 423
Recovered: 0
India
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Deaths: 459 652
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Brazil
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Deaths: 608 235
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Deaths: 141 607
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Russia
Russia
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Deaths: 237 619
Recovered: 0
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