Does NICOTINE Cause Product dose omission issue? 115 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 115 reports of Product dose omission issue have been filed in association with NICOTINE (Nicotine Polacrilex). This represents 0.4% of all adverse event reports for NICOTINE.
115
Reports of Product dose omission issue with NICOTINE
0.4%
of all NICOTINE reports
0
Deaths
5
Hospitalizations
How Dangerous Is Product dose omission issue From NICOTINE?
Of the 115 reports, 5 (4.3%) required hospitalization.
Is Product dose omission issue Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for NICOTINE. However, 115 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 issue?
DUPILUMAB (18,189)
USTEKINUMAB (9,405)
GUSELKUMAB (9,267)
LENALIDOMIDE (8,145)
MEPOLIZUMAB (5,873)
TOFACITINIB (5,646)
VOXELOTOR (5,122)
BELIMUMAB (4,671)
SECUKINUMAB (4,572)
APREMILAST (4,460)
Which NICOTINE Alternatives Have Lower Product dose omission issue Risk?
NICOTINE vs NIFEDIPINE
NICOTINE vs NILOTINIB
NICOTINE vs NIMESULIDE
NICOTINE vs NIMODIPINE
NICOTINE vs NINTEDANIB