Does OMEPRAZOLE Cause Product dose omission issue? 296 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 296 reports of Product dose omission issue have been filed in association with OMEPRAZOLE (omeprazole sodium bicarbonate). This represents 0.3% of all adverse event reports for OMEPRAZOLE.
296
Reports of Product dose omission issue with OMEPRAZOLE
0.3%
of all OMEPRAZOLE reports
53
Deaths
135
Hospitalizations
How Dangerous Is Product dose omission issue From OMEPRAZOLE?
Of the 296 reports, 53 (17.9%) resulted in death, 135 (45.6%) required hospitalization, and 36 (12.2%) were considered life-threatening.
Is Product dose omission issue Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for OMEPRAZOLE. However, 296 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 dose omission issue?
DUPILUMAB (18,189)
USTEKINUMAB (9,405)
GUSELKUMAB (9,267)
LENALIDOMIDE (8,145)
MEPOLIZUMAB (5,873)
TOFACITINIB (5,646)
VOXELOTOR (5,122)
BELIMUMAB (4,671)
SECUKINUMAB (4,572)
APREMILAST (4,460)
Which OMEPRAZOLE Alternatives Have Lower Product dose omission issue Risk?
OMEPRAZOLE vs OMEPRAZOLE\SODIUM BICARBONATE
OMEPRAZOLE vs OMNIPAQUE
OMEPRAZOLE vs OMNISCAN
OMEPRAZOLE vs ONABOTULINUMTOXINA
OMEPRAZOLE vs ONASEMNOGENE ABEPARVOVEC