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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 Device defective? 7 Reports in FDA Database

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According to the FDA Adverse Event Reporting System (FAERS), 7 reports of Device defective have been filed in association with OMEPRAZOLE (omeprazole sodium bicarbonate). This represents 0.0% of all adverse event reports for OMEPRAZOLE.

7
Reports of Device defective with OMEPRAZOLE
0.0%
of all OMEPRAZOLE reports
0
Deaths
0
Hospitalizations

How Dangerous Is Device defective From OMEPRAZOLE?

Of the 7 reports.

Is Device defective Listed in the Official Label?

This adverse event is not currently listed in the official FDA drug label for OMEPRAZOLE. However, 7 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 Device defective?

SOMATROPIN (1,719) USTEKINUMAB (1,071) SECUKINUMAB (666) GUSELKUMAB (574) GOLIMUMAB (539) ABATACEPT (458) ALBUTEROL (445) TOCILIZUMAB (400) INSULIN GLARGINE (397) EXENATIDE (387)

Which OMEPRAZOLE Alternatives Have Lower Device defective 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 Device defective Reports All Drugs Causing Device defective OMEPRAZOLE Demographics