Does OMEPRAZOLE Cause Device issue? 78 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 78 reports of Device issue have been filed in association with OMEPRAZOLE (omeprazole sodium bicarbonate). This represents 0.1% of all adverse event reports for OMEPRAZOLE.
78
Reports of Device issue with OMEPRAZOLE
0.1%
of all OMEPRAZOLE reports
0
Deaths
16
Hospitalizations
How Dangerous Is Device issue From OMEPRAZOLE?
Of the 78 reports, 16 (20.5%) required hospitalization, and 2 (2.6%) were considered life-threatening.
Is Device issue Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for OMEPRAZOLE. However, 78 reports have been filed with the FAERS database.
What Other Side Effects Does OMEPRAZOLE Cause?
Chronic kidney disease (35,759)
Acute kidney injury (19,260)
Renal failure (14,721)
End stage renal disease (10,356)
Renal injury (9,482)
Tubulointerstitial nephritis (4,809)
Drug ineffective (4,355)
Gastrooesophageal reflux disease (3,929)
Pain (3,602)
Nephrogenic anaemia (2,873)
What Other Drugs Cause Device issue?
ADALIMUMAB (17,630)
SOMATROPIN (5,131)
PEGFILGRASTIM (5,071)
ETANERCEPT (4,143)
INSULIN GLARGINE (3,175)
EXENATIDE (2,862)
LEVONORGESTREL (2,623)
CARBIDOPA\LEVODOPA (2,574)
GOLIMUMAB (1,827)
USTEKINUMAB (1,716)
Which OMEPRAZOLE Alternatives Have Lower Device issue Risk?
OMEPRAZOLE vs OMEPRAZOLE\SODIUM BICARBONATE
OMEPRAZOLE vs OMNIPAQUE
OMEPRAZOLE vs OMNISCAN
OMEPRAZOLE vs ONABOTULINUMTOXINA
OMEPRAZOLE vs ONASEMNOGENE ABEPARVOVEC