Does ZEGERID OTC Cause Product quality issue? 6 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 6 reports of Product quality issue have been filed in association with ZEGERID OTC. This represents 10.0% of all adverse event reports for ZEGERID OTC.
6
Reports of Product quality issue with ZEGERID OTC
10.0%
of all ZEGERID OTC reports
0
Deaths
0
Hospitalizations
How Dangerous Is Product quality issue From ZEGERID OTC?
Of the 6 reports.
Is Product quality issue Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for ZEGERID OTC. However, 6 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 physical issue (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)