Tocilizumab-induced pancreatitis: case report and review of data from the FDA Adverse Event Reporting System

Author:

Flaig T.1,Douros A.1,Bronder E.1,Klimpel A.1,Kreutz R.1,Garbe E.23

Affiliation:

1. Department of Clinical Pharmacology and Toxicology; Charité-Universitätsmedizin Berlin; Berlin Germany

2. Leibniz Institute for Prevention Research and Epidemiology BIPS; Bremen Germany

3. Faculty of Human and Health Sciences; University of Bremen; Bremen Germany

Funder

Federal Institute for Drugs and Medical Devices

GlaxoSmithKline

Bayer

Mundipharma

Novartis

Teva

Takeda Pharmaceuticals U.S.A.

Sanofi

Celgene

Bayer Pharma

Berlin Chemie Menarini

Bristol-Myers Squibb

Daiichi-Sankyo

Servier

Publisher

Wiley

Subject

Pharmacology (medical),Pharmacology

Reference33 articles.

1. Drug-induced pancreatitis;Nitsche;Curr Gastroenterol Rep,2012

2. Drug-induced pancreatitis: incidence, management and prevention;Balani;Drug Saf,2008

3. Incidence, severity, and etiology of drug-induced acute pancreatitis;Vinklerova;Dig Dis Sci,2010

4. Discrepancies between population-based data and adverse reaction reports in assessing drugs as causes of acute pancreatitis;Lancashire;Aliment Pharmacol Ther,2003

5. Risk of acute pancreatitis in users of azathioprine: a population-based case-control study;Floyd;Am J Gastroenterol,2003

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