Liver safety of tolvaptan in patients with autosomal dominant polycystic kidney disease: interim data from a post-authorization safety study
ABSTRACT Background After the risk of drug-induced liver injury was detected during tolvaptan clinical development for the treatment of autosomal dominant polycystic kidney disease (ADPKD), a post-marketing pharmacovigilance study was required for European Union regulatory approval. Methods This is...
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Veröffentlicht in: | Clinical kidney journal 2024-11, Vol.17 (11), p.sfae324 |
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Sprache: | eng |
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