Tolvaptan and Number Needed to Harm in Autosomal Dominant Polycystic Kidney Disease
Main Authors: | Keith A. Betts, PhD, Sasikiran Nunna, PhD, Retesh Kumar, MD, Xiaoyu Nie, PhD, Ancilla W. Fernandes, PhD |
---|---|
Format: | Article |
Language: | English |
Published: |
Elsevier
2024-04-01
|
Series: | Kidney Medicine |
Online Access: | http://www.sciencedirect.com/science/article/pii/S259005952400013X |
Similar Items
-
Effects of tolvaptan discontinuation in patients with autosomal dominant polycystic kidney disease: a post hoc pooled analysis
by: Michael Lioudis, et al.
Published: (2023-06-01) -
Bacterial Cholangitis in Autosomal Dominant Polycystic Kidney and Liver Disease
by: William P. Martin, MBChB, MSc, et al.
Published: (2019-06-01) -
Tolvaptan in the treatment of autosomal dominant polycystic kidney disease: patient selection and special considerations
by: Sans-Atxer L, et al.
Published: (2018-01-01) -
Clinical Utility and Tolerability of Tolvaptan in the Treatment of Autosomal Dominant Polycystic Kidney Disease (ADPKD)
by: Raina R, et al.
Published: (2022-09-01) -
Quality of Life in Autosomal Dominant Polycystic Kidney Disease Patients Treated With Tolvaptan
by: Manuel A. Anderegg, et al.
Published: (2020-03-01)