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FDA Requires Stronger Peripheral Neuropathy Warning for Quinolones

The Food and Drug Administration is requiring a stronger warning about the potential for peripheral neuropathy with fluoroquinolone antibiotics that are taken orally or by injection. The warning does not apply to topical formulations, which have not been associated with neuropathy. Drug labels and patient medication guides must be updated, said the agency.  READ MORE

Source: ACS Surgery News