Does NICOTINE Cause Incorrect product administration duration? 264 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 264 reports of Incorrect product administration duration have been filed in association with NICOTINE (Nicotine Polacrilex). This represents 0.8% of all adverse event reports for NICOTINE.
264
Reports of Incorrect product administration duration with NICOTINE
0.8%
of all NICOTINE reports
1
Deaths
2
Hospitalizations
How Dangerous Is Incorrect product administration duration From NICOTINE?
Of the 264 reports, 1 (0.4%) resulted in death, 2 (0.8%) required hospitalization.
Is Incorrect product administration duration Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for NICOTINE. However, 264 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 Incorrect product administration duration?
ETONOGESTREL (3,974)
POLYETHYLENE GLYCOL 3350 (2,129)
NIRMATRELVIR\RITONAVIR (744)
DOCOSANOL (634)
LANSOPRAZOLE (564)
LOPERAMIDE (543)
NAPROXEN (499)
INSULIN LISPRO (479)
DICLOFENAC (362)
OMEPRAZOLE (302)
Which NICOTINE Alternatives Have Lower Incorrect product administration duration Risk?
NICOTINE vs NIFEDIPINE
NICOTINE vs NILOTINIB
NICOTINE vs NIMESULIDE
NICOTINE vs NIMODIPINE
NICOTINE vs NINTEDANIB