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WASHINGTON — Federal regulators have warned Pfizer for failing to promptly report complaints with its drugs that may have involved serious injury.
Pfizer repeatedly failed to submit product complaints to the Food and Drug Administration within the required 15 days, according to an FDA warning letter obtained by The Associated Press.
In some cases, Pfizer failed to report problems altogether, including reports of serious side effects with the cholesterol drug Lipitor and the anti-seizure drug Lyrica.
