RT @RheumNow: FDA Adverse Event Reporting System (FAERS) data on upadacitinib found the top Serious AE to be UTI (2.7%), H zoster (1.6%), d…
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RT @RheumNow: FDA Adverse Event Reporting System (FAERS) data on upadacitinib found the top Serious AE to be UTI (2.7%), H zoster (1.6%), d…
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FDA Adverse Event Reporting System (FAERS) data on upadacitinib found the top Serious AE to be UTI (2.7%), H zoster (1.6%), diverticulitis (1.2%), bronchitis (0.7%), nasopharyngitis (0.7%), nephrolithiasis (0.7%), PE (0.7%), PJP pneumonia (0.5%) https://t.
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RT @FrontPharmacol: New Research: A real-world pharmacovigilance analysis of FDA adverse event reporting system database for upadacitinib #…