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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 ZANTAC Cause Product quality issue? 7 Reports in FDA Database

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According to the FDA Adverse Event Reporting System (FAERS), 7 reports of Product quality issue have been filed in association with ZANTAC. This represents 3.6% of all adverse event reports for ZANTAC.

7
Reports of Product quality issue with ZANTAC
3.6%
of all ZANTAC reports
0
Deaths
0
Hospitalizations

How Dangerous Is Product quality issue From ZANTAC?

Of the 7 reports.

Is Product quality issue Listed in the Official Label?

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

What Other Side Effects Does ZANTAC Cause?

Drug ineffective (29) Off label use (20) Dyspepsia (10) Dyspnoea (10) Gastrooesophageal reflux disease (10) Headache (9) Nausea (9) Drug hypersensitivity (8) Diarrhoea (7) Dizziness (7)

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 ZANTAC Alternatives Have Lower Product quality issue Risk?

ZANTAC vs ZANTAC 150 ZANTAC vs ZANUBRUTINIB ZANTAC vs ZAVEGEPANT ZANTAC vs ZEAXANTHIN ZANTAC vs ZELBORAF

Related Pages

ZANTAC Full Profile All Product quality issue Reports All Drugs Causing Product quality issue ZANTAC Demographics