Does OMEPRAZOLE Cause Product quality issue? 594 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 594 reports of Product quality issue have been filed in association with OMEPRAZOLE (omeprazole sodium bicarbonate). This represents 0.7% of all adverse event reports for OMEPRAZOLE.
594
Reports of Product quality issue with OMEPRAZOLE
0.7%
of all OMEPRAZOLE reports
8
Deaths
42
Hospitalizations
How Dangerous Is Product quality issue From OMEPRAZOLE?
Of the 594 reports, 8 (1.3%) resulted in death, 42 (7.1%) required hospitalization, and 12 (2.0%) were considered life-threatening.
Is Product quality issue Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for OMEPRAZOLE. However, 594 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 quality issue?
ETONOGESTREL (4,651)
ALBUTEROL (4,466)
TIOTROPIUM (3,821)
MOMETASONE FUROATE (3,406)
LIDOCAINE (3,126)
FLUTICASONE\SALMETEROL (2,986)
FORMOTEROL\MOMETASONE FUROATE (2,458)
FENTANYL (2,450)
NICOTINE (1,987)
EXENATIDE (1,839)
Which OMEPRAZOLE Alternatives Have Lower Product quality issue Risk?
OMEPRAZOLE vs OMEPRAZOLE\SODIUM BICARBONATE
OMEPRAZOLE vs OMNIPAQUE
OMEPRAZOLE vs OMNISCAN
OMEPRAZOLE vs ONABOTULINUMTOXINA
OMEPRAZOLE vs ONASEMNOGENE ABEPARVOVEC