Does OMEPRAZOLE Cause Product label issue? 32 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 32 reports of Product label issue have been filed in association with OMEPRAZOLE (omeprazole sodium bicarbonate). This represents 0.0% of all adverse event reports for OMEPRAZOLE.
32
Reports of Product label issue with OMEPRAZOLE
0.0%
of all OMEPRAZOLE reports
0
Deaths
1
Hospitalizations
How Dangerous Is Product label issue From OMEPRAZOLE?
Of the 32 reports, 1 (3.1%) required hospitalization, and 1 (3.1%) were considered life-threatening.
Is Product label issue Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for OMEPRAZOLE. However, 32 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 Product label issue?
RIVAROXABAN (379)
ACETAMINOPHEN (276)
GUSELKUMAB (177)
USTEKINUMAB (164)
DIMETHICONE\LOPERAMIDE (154)
CETIRIZINE (138)
IBUPROFEN (99)
GOLIMUMAB (76)
POLYETHYLENE GLYCOL 3350 (76)
FENTANYL (72)
Which OMEPRAZOLE Alternatives Have Lower Product label issue Risk?
OMEPRAZOLE vs OMEPRAZOLE\SODIUM BICARBONATE
OMEPRAZOLE vs OMNIPAQUE
OMEPRAZOLE vs OMNISCAN
OMEPRAZOLE vs ONABOTULINUMTOXINA
OMEPRAZOLE vs ONASEMNOGENE ABEPARVOVEC