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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 NICORETTE Cause Product quality issue? 5 Reports in FDA Database

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According to the FDA Adverse Event Reporting System (FAERS), 5 reports of Product quality issue have been filed in association with NICORETTE. This represents 14.7% of all adverse event reports for NICORETTE.

5
Reports of Product quality issue with NICORETTE
14.7%
of all NICORETTE reports
0
Deaths
0
Hospitalizations

How Dangerous Is Product quality issue From NICORETTE?

Of the 5 reports.

Is Product quality issue Listed in the Official Label?

This adverse event is not currently listed in the official FDA drug label for NICORETTE. However, 5 reports have been filed with the FAERS database.

What Other Side Effects Does NICORETTE Cause?

Drug administration error (7) Drug ineffective (5) Intentional drug misuse (5)

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)

Related Pages

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