Elevated serum uric acid level was a notable adverse event during combination therapy with sofosbuvir and ribavirin

Author:

Sato Ken12,Naganuma Atsushi3ORCID,Nagashima Tamon4,Hoshino Takashi3,Uehara Daisuke3,Arai Yousuke4,Horiuchi Katsuhiko5,Yuasa Kazuhisa5,Takayama Hisashi6,Arai Hirotaka6,Hatanaka Takeshi3,Ohyama Tatsuya1,Tahara Hiroki5,Sohara Naondo3,Kobayashi Takeshi12,Horiguchi Norio12,Yamazaki Yuichi12,Kakizaki Satoru12,Kusano Motoyasu7,Yamada Masanobu1,Murase Takayo8,Nakamura Takashi8

Affiliation:

1. Department of Medicine and Molecular Science Gunma University Graduate School of Medicine Maebashi Japan

2. Department of Hepatology Heisei Hidaka Clinic Takasaki Japan

3. Department of Gastroenterology Takasaki General Medical Center, National Hospital Organization Takasaki Japan

4. Department of Gastroenterology Shibukawa General Medical Center, National Hospital Organization Shibukawa Japan

5. Department of Gastroenterology Gunma Chuo Hospital Maebashi Japan

6. Department of Gastroenterology Maebashi Red Cross Hospital Maebashi Japan

7. Department of Endoscopy and Endoscopic Surgery Gunma University Hospital Maebashi Japan

8. Sanwa Kagaku Kenkyusho Co., Ltd. Inaba Japan

Publisher

Wiley

Subject

Infectious Diseases,Hepatology

Reference17 articles.

1. Sofosbuvir plus ribavirin in Japanese patients with chronic genotype 2 HCV infection: an open‐label, phase 3 trial

2. A highly sensitive assay of human plasma xanthine oxidoreductase activity using stable isotope-labeled xanthine and LC/TQMS

3. Severe Interferon/Ribavirin‐Induced Hyperuricemia and Urate Nephropathy Requiring Rasburicase and Hemodialysis in a Liver Transplant Recipient;Knorr JP;Exp Clin Transplant,2015

4. Interview form of SOVALDI tablets 400 mg 6th edn.2017;71–72(in Japanese).

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