Real-World Pharmacovigilance Study Identifies Drugs Linked to Hepatitis B Virus Reactivation.

J Med Virol

State Key Laboratory for Diagnosis and Treatment of Infectious Diseases, National Clinical Research Center for Infectious Diseases, National Medical Center for Infectious Diseases, Collaborative Innovation Center for Diagnosis and Treatment of Infectious Diseases, The First Affiliated Hospital, Zhejiang University School of Medicine, Hangzhou, China.

Published: November 2024

AI Article Synopsis

  • Hepatitis B virus reactivation (HBVr) is a serious issue linked to various drugs, but the specific drugs involved aren’t well-documented.
  • A study analyzed data from FDA and Japanese databases and found 44 drugs related to HBVr, with 35 lacking safety warnings on their labels; most were cancer and immune system medications.
  • The research highlighted early HBVr occurrences with certain drugs and identified safer alternatives (like entecavir and tenofovir) to help improve patient care and safety.

Article Abstract

Hepatitis B virus reactivation (HBVr) can be a serious clinical complication that has not been fully characterized in terms of the drugs associated with this adverse effect. Leveraging the expansive data available in the FDA Adverse Event Reporting System (FAERS) and the Japanese Adverse Drug Event Report (JADER) databases, we conducted a retrospective analysis to identify drugs significantly linked to HBVr using three disproportionality analyses. Our study identified 44 drugs associated with HBVr, of which 35 did not have warnings in their product labels. The majority of these drugs were antineoplastic and immunomodulating agents, with a tendency for early occurrence of HBVr, particularly among antineoplastic agents and systemic corticosteroids. Additionally, entecavir, tenofovir disoproxil and tenofovir alafenamide demonstrated better safety profiles in preventing HBVr. These findings enhance our understanding of the demographic characteristics of patients at risk for HBVr, the drugs that pose a high risk for HBVr, the timing of such events, and the appropriate preventive medications. This knowledge contributes to the development of better prevention and treatment strategies, ultimately optimizing patient outcomes.

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Source
http://dx.doi.org/10.1002/jmv.70055DOI Listing

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