Does OMEPRAZOLE Cause Wrong product administered? 67 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 67 reports of Wrong product administered have been filed in association with OMEPRAZOLE (omeprazole sodium bicarbonate). This represents 0.1% of all adverse event reports for OMEPRAZOLE.
67
Reports of Wrong product administered with OMEPRAZOLE
0.1%
of all OMEPRAZOLE reports
2
Deaths
29
Hospitalizations
How Dangerous Is Wrong product administered From OMEPRAZOLE?
Of the 67 reports, 2 (3.0%) resulted in death, 29 (43.3%) required hospitalization.
Is Wrong product administered Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for OMEPRAZOLE. However, 67 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 Wrong product administered?
INSULIN LISPRO (337)
INSULIN GLARGINE (226)
RISPERIDONE (141)
QUETIAPINE (137)
ACETAMINOPHEN (133)
INSULIN ASPART (112)
CLOZAPINE (106)
INSULIN HUMAN (104)
TUBERCULIN PURIFIED PROTEIN DERIVATIVE (104)
IBUPROFEN (102)
Which OMEPRAZOLE Alternatives Have Lower Wrong product administered Risk?
OMEPRAZOLE vs OMEPRAZOLE\SODIUM BICARBONATE
OMEPRAZOLE vs OMNIPAQUE
OMEPRAZOLE vs OMNISCAN
OMEPRAZOLE vs ONABOTULINUMTOXINA
OMEPRAZOLE vs ONASEMNOGENE ABEPARVOVEC