Does OMEPRAZOLE Cause Product dispensing error? 109 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 109 reports of Product dispensing error have been filed in association with OMEPRAZOLE (omeprazole sodium bicarbonate). This represents 0.1% of all adverse event reports for OMEPRAZOLE.
109
Reports of Product dispensing error with OMEPRAZOLE
0.1%
of all OMEPRAZOLE reports
19
Deaths
34
Hospitalizations
How Dangerous Is Product dispensing error From OMEPRAZOLE?
Of the 109 reports, 19 (17.4%) resulted in death, 34 (31.2%) required hospitalization, and 7 (6.4%) were considered life-threatening.
Is Product dispensing error Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for OMEPRAZOLE. However, 109 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 dispensing error?
INSULIN GLARGINE (1,048)
FLUTICASONE FUROATE\UMECLIDINIUM\VILANTEROL TRIFENATATE (692)
ADALIMUMAB (386)
SEMAGLUTIDE (379)
PREGABALIN (323)
NIRMATRELVIR\RITONAVIR (310)
ETANERCEPT (305)
SECUKINUMAB (300)
APIXABAN (299)
PALBOCICLIB (299)
Which OMEPRAZOLE Alternatives Have Lower Product dispensing error Risk?
OMEPRAZOLE vs OMEPRAZOLE\SODIUM BICARBONATE
OMEPRAZOLE vs OMNIPAQUE
OMEPRAZOLE vs OMNISCAN
OMEPRAZOLE vs ONABOTULINUMTOXINA
OMEPRAZOLE vs ONASEMNOGENE ABEPARVOVEC