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Important: This site presents data from the FDA Adverse Event Reporting System (FAERS). A report does not mean the drug caused the event. Full disclaimer.

Does OMEPRAZOLE Cause Product solubility abnormal? 41 Reports in FDA Database

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According to the FDA Adverse Event Reporting System (FAERS), 41 reports of Product solubility abnormal have been filed in association with OMEPRAZOLE (omeprazole sodium bicarbonate). This represents 0.1% of all adverse event reports for OMEPRAZOLE.

41
Reports of Product solubility abnormal with OMEPRAZOLE
0.1%
of all OMEPRAZOLE reports
0
Deaths
0
Hospitalizations

How Dangerous Is Product solubility abnormal From OMEPRAZOLE?

Of the 41 reports.

Is Product solubility abnormal Listed in the Official Label?

This adverse event is not currently listed in the official FDA drug label for OMEPRAZOLE. However, 41 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 solubility abnormal?

BUPRENORPHINE (498) BUPRENORPHINE\NALOXONE (274) POLYETHYLENE GLYCOL 3350 (220) CHOLESTYRAMINE (193) PATIROMER (107) LEVOTHYROXINE (100) SOMATROPIN (98) EXENATIDE (97) ESTRADIOL (94) NITROGLYCERIN (81)

Which OMEPRAZOLE Alternatives Have Lower Product solubility abnormal Risk?

OMEPRAZOLE vs OMEPRAZOLE\SODIUM BICARBONATE OMEPRAZOLE vs OMNIPAQUE OMEPRAZOLE vs OMNISCAN OMEPRAZOLE vs ONABOTULINUMTOXINA OMEPRAZOLE vs ONASEMNOGENE ABEPARVOVEC

Related Pages

OMEPRAZOLE Full Profile All Product solubility abnormal Reports All Drugs Causing Product solubility abnormal OMEPRAZOLE Demographics