4.2 Review

Medication safety in chronic kidney disease

Journal

CURRENT OPINION IN NEPHROLOGY AND HYPERTENSION
Volume 32, Issue 5, Pages 434-438

Publisher

LIPPINCOTT WILLIAMS & WILKINS
DOI: 10.1097/MNH.0000000000000907

Keywords

acute kidney injury; chronic kidney disease; drug safety; medication safety

Ask authors/readers for more resources

The purpose of this review is to summarize recent evidence on drugs that increase the risk of nephrotoxicity, progression of chronic kidney disease (CKD), or drug-induced harm in CKD patients. Several medications increase the risk of acute kidney injury or CKD progression, and it is important to pay close attention to selecting appropriate doses or safer alternatives to reduce the risk of drug-induced harm in CKD patients.
Purpose of reviewSeveral drugs cause nephrotoxicity and accelerate progression of chronic kidney disease (CKD). The objective of this review is to summarize recent evidence on drugs that either increase the risk of nephrotoxicity, progression of CKD or drug induced harm in patients with CKD.Recent findingsBisphosphonates and hypnotics increase the progression of CKD, whereas denosumab does not accelerate progression of CKD. Tenofovir disoproxil fumarate (TDF) increases the risk of renal tubular toxicity and adverse effects on bone, but Tenofovir alafenamide (TAF) and Tenofovir amibufenamide (TMF) have favorable safety profile on the kidneys and bones. Although no dosage adjustment is needed for Oral Nirmatrelvir/Ritonavir in patients with mild renal impairment and coronavirus disease 2019, the dosage is reduced to twice daily in those with moderate renal impairment. It is not recommended in patients with severe renal impairment. The prescribing information does not recommend use of remdesevir below glomerular filtration rate (eGFR) < 30 ml/min but recent studies suggest that remdesevir may be safe and effective in patients with varying levels of CKD severity. Molnupiravir does not require dose adjustment in patients with CKD.Several medications increase the risk of development of acute kidney injury or progression of CKD. Close attention is needed to select the appropriate dose or safer alternatives to reduce the risk of drug-induced harm in patients with CKD.

Authors

I am an author on this paper
Click your name to claim this paper and add it to your profile.

Reviews

Primary Rating

4.2
Not enough ratings

Secondary Ratings

Novelty
-
Significance
-
Scientific rigor
-
Rate this paper

Recommended

No Data Available
No Data Available