Does BUDESONIDE Cause Tubulointerstitial nephritis? 167 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 167 reports of Tubulointerstitial nephritis have been filed in association with BUDESONIDE (BREYNA). This represents 0.7% of all adverse event reports for BUDESONIDE.
167
Reports of Tubulointerstitial nephritis with BUDESONIDE
0.7%
of all BUDESONIDE reports
0
Deaths
24
Hospitalizations
How Dangerous Is Tubulointerstitial nephritis From BUDESONIDE?
Of the 167 reports, 24 (14.4%) required hospitalization, and 2 (1.2%) were considered life-threatening.
Is Tubulointerstitial nephritis Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for BUDESONIDE. However, 167 reports have been filed with the FAERS database.
What Other Side Effects Does BUDESONIDE Cause?
Asthma (4,544)
Dyspnoea (4,441)
Drug ineffective (4,384)
Off label use (3,033)
Wheezing (2,590)
Cough (2,269)
Therapeutic product effect incomplete (2,191)
Loss of personal independence in daily activities (1,890)
Condition aggravated (1,548)
Fatigue (1,508)
What Other Drugs Cause Tubulointerstitial nephritis?
OMEPRAZOLE (4,809)
ESOMEPRAZOLE (4,024)
LANSOPRAZOLE (3,860)
PANTOPRAZOLE (3,590)
DEXLANSOPRAZOLE (2,177)
RABEPRAZOLE (1,125)
PEMBROLIZUMAB (860)
IBUPROFEN (844)
VANCOMYCIN (523)
TACROLIMUS (486)
Which BUDESONIDE Alternatives Have Lower Tubulointerstitial nephritis Risk?
BUDESONIDE vs BUDESONIDE\FORMOTEROL
BUDESONIDE vs BUDESONIDE\FORMOTEROL\GLYCOPYRROLATE
BUDESONIDE vs BUDESONIDE\FORMOTEROL\GLYCOPYRRONIUM
BUDESONIDE vs BUMETANIDE
BUDESONIDE vs BUPIVACAINE