Physician-Patient Communication about Novel Drugs and High-Risk Medical Devices.
PMID: 39707817 ·
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Abstract
After a new drug or medical device is approved by the US Food and Drug Administration (FDA), physician-patient communication about benefits and risks is critical, including whether the product was approved through an expedited pathway based on limited evidence. In addition, physician reporting of drug- and device-related adverse events in real-world use is necessary to have a complete safety profile. We studied physician-reported communication and safety-reporting practices related to drugs and
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Official Source
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