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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 ZEGERID OTC Cause Product physical issue? 7 Reports in FDA Database

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According to the FDA Adverse Event Reporting System (FAERS), 7 reports of Product physical issue have been filed in association with ZEGERID OTC. This represents 11.7% of all adverse event reports for ZEGERID OTC.

7
Reports of Product physical issue with ZEGERID OTC
11.7%
of all ZEGERID OTC reports
0
Deaths
0
Hospitalizations

How Dangerous Is Product physical issue From ZEGERID OTC?

Of the 7 reports.

Is Product physical issue Listed in the Official Label?

This adverse event is not currently listed in the official FDA drug label for ZEGERID OTC. However, 7 reports have been filed with the FAERS database.

What Other Side Effects Does ZEGERID OTC Cause?

Drug ineffective (13) Incorrect drug administration duration (13) Off label use (11) Overdose (11) Inappropriate schedule of drug administration (9) Product quality issue (6)

What Other Drugs Cause Product physical issue?

SUMATRIPTAN (2,349) TIOTROPIUM (807) ICOSAPENT ETHYL (666) LISDEXAMFETAMINE DIMESYLATE (652) AMPHETAMINE ASPARTATE\AMPHETAMINE\DEXTROAMPHETAMINE SACCHARATE\DEXTROAMPHETAMINE (387) IBUPROFEN (337) ESTRADIOL\LEVONORGESTREL (305) ESTRADIOL (302) RUXOLITINIB (302) IXAZOMIB (298)

Related Pages

ZEGERID OTC Full Profile All Product physical issue Reports All Drugs Causing Product physical issue ZEGERID OTC Demographics