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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 FRESHMINT Cause Product quality issue? 8 Reports in FDA Database

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According to the FDA Adverse Event Reporting System (FAERS), 8 reports of Product quality issue have been filed in association with NICORETTE FRESHMINT. This represents 15.1% of all adverse event reports for NICORETTE FRESHMINT.

8
Reports of Product quality issue with NICORETTE FRESHMINT
15.1%
of all NICORETTE FRESHMINT reports
0
Deaths
0
Hospitalizations

How Dangerous Is Product quality issue From NICORETTE FRESHMINT?

Of the 8 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 FRESHMINT. However, 8 reports have been filed with the FAERS database.

What Other Side Effects Does NICORETTE FRESHMINT Cause?

Intentional drug misuse (29) Drug administration error (13) Drug ineffective (8) Nicotine dependence (7) Nausea (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 FRESHMINT Full Profile All Product quality issue Reports All Drugs Causing Product quality issue NICORETTE FRESHMINT Demographics