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Clinicians Report Medication Harms at “Personal and Professional Peril” Clinicians were sued by the pharmaceutical industry, received verbal threats, and at least one lost his job after reporting adverse effects. 2022 A new study documents what happens after clinicians report “very serious adverse drug/device reactions (ADRs)” of medications experienced by their patients. To be defined as a “very serious ADR,” it had to be caused by “severe toxicity,” according to the researchers. They focused on drugs with large settlements and large numbers of documented harmed patients. This ensures that the reported events were true and accurate. The paper revealed that even after clinicians made these reports, there was a long delay before the pharmaceutical company responsible would admit the harms to regulators. Eventually, these reports cost the pharmaceutical industry tens of billions of dollars in fines and lawsuits. But before then, the clinician

United statesNoord hollandCharlesl bennettEricj topolNancy olivieriSouthern network on adverse reactionsUniversity of south carolina college pharmacySouth carolina collegeSouthern networkAdverse reactionsJay amsterdamSafety monitoring boardsஒன்றுபட்டது மாநிலங்களில்நூற்த் ஹாலண்ட்நான்சி ஆலிவேரிபல்கலைக்கழகம் ஆஃப் தெற்கு கரோலினா கல்லூரி மருந்தகம்