Does OMEPRAZOLE Cause Incorrect product administration duration? 302 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 302 reports of Incorrect product administration duration have been filed in association with OMEPRAZOLE (omeprazole sodium bicarbonate). This represents 0.4% of all adverse event reports for OMEPRAZOLE.
302
Reports of Incorrect product administration duration with OMEPRAZOLE
0.4%
of all OMEPRAZOLE reports
1
Deaths
24
Hospitalizations
How Dangerous Is Incorrect product administration duration From OMEPRAZOLE?
Of the 302 reports, 1 (0.3%) resulted in death, 24 (7.9%) required hospitalization, and 2 (0.7%) were considered life-threatening.
Is Incorrect product administration duration Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for OMEPRAZOLE. However, 302 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 Incorrect product administration duration?
ETONOGESTREL (3,974)
POLYETHYLENE GLYCOL 3350 (2,129)
NIRMATRELVIR\RITONAVIR (744)
DOCOSANOL (634)
LANSOPRAZOLE (564)
LOPERAMIDE (543)
NAPROXEN (499)
INSULIN LISPRO (479)
DICLOFENAC (362)
ALENDRONATE (287)
Which OMEPRAZOLE Alternatives Have Lower Incorrect product administration duration Risk?
OMEPRAZOLE vs OMEPRAZOLE\SODIUM BICARBONATE
OMEPRAZOLE vs OMNIPAQUE
OMEPRAZOLE vs OMNISCAN
OMEPRAZOLE vs ONABOTULINUMTOXINA
OMEPRAZOLE vs ONASEMNOGENE ABEPARVOVEC