Does OMEPRAZOLE Cause Product prescribing issue? 30 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 30 reports of Product prescribing issue have been filed in association with OMEPRAZOLE (omeprazole sodium bicarbonate). This represents 0.0% of all adverse event reports for OMEPRAZOLE.
30
Reports of Product prescribing issue with OMEPRAZOLE
0.0%
of all OMEPRAZOLE reports
4
Deaths
17
Hospitalizations
How Dangerous Is Product prescribing issue From OMEPRAZOLE?
Of the 30 reports, 4 (13.3%) resulted in death, 17 (56.7%) required hospitalization, and 9 (30.0%) were considered life-threatening.
Is Product prescribing issue Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for OMEPRAZOLE. However, 30 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 prescribing issue?
DUPILUMAB (1,715)
POLYETHYLENE GLYCOL 3350 (1,439)
LENALIDOMIDE (948)
OXYCODONE (646)
RIVAROXABAN (359)
ACETAMINOPHEN\OXYCODONE (347)
ETONOGESTREL (311)
ACETAMINOPHEN\HYDROCODONE (298)
CERTOLIZUMAB PEGOL (297)
CABOZANTINIB S-MALATE (294)
Which OMEPRAZOLE Alternatives Have Lower Product prescribing issue Risk?
OMEPRAZOLE vs OMEPRAZOLE\SODIUM BICARBONATE
OMEPRAZOLE vs OMNIPAQUE
OMEPRAZOLE vs OMNISCAN
OMEPRAZOLE vs ONABOTULINUMTOXINA
OMEPRAZOLE vs ONASEMNOGENE ABEPARVOVEC