Does NICOTINE Cause Product dose omission? 245 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 245 reports of Product dose omission have been filed in association with NICOTINE (Nicotine Polacrilex). This represents 0.8% of all adverse event reports for NICOTINE.
245
Reports of Product dose omission with NICOTINE
0.8%
of all NICOTINE reports
0
Deaths
0
Hospitalizations
How Dangerous Is Product dose omission From NICOTINE?
Of the 245 reports.
Is Product dose omission Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for NICOTINE. However, 245 reports have been filed with the FAERS database.
What Other Side Effects Does NICOTINE Cause?
Drug ineffective (5,690)
Nicotine dependence (3,699)
Nausea (2,162)
Product adhesion issue (2,133)
Application site pruritus (2,074)
Application site erythema (2,004)
Product quality issue (1,987)
Wrong technique in product usage process (1,673)
Treatment noncompliance (1,382)
Malaise (1,183)
What Other Drugs Cause Product dose omission?
APREMILAST (4,567)
DUPILUMAB (2,729)
ALBUTEROL (1,742)
USTEKINUMAB (1,653)
INSULIN GLARGINE (1,500)
ETANERCEPT (1,400)
LENALIDOMIDE (1,400)
RUXOLITINIB (1,376)
ALIROCUMAB (1,354)
DIMETHYL (1,248)
Which NICOTINE Alternatives Have Lower Product dose omission Risk?
NICOTINE vs NIFEDIPINE
NICOTINE vs NILOTINIB
NICOTINE vs NIMESULIDE
NICOTINE vs NIMODIPINE
NICOTINE vs NINTEDANIB