NICOTINE
Generic: NICOTINE, NICOTINE TRANSDERMAL SYSTEM
MeijerManufacturer
TRANSDERMALRoute
NICOTINEActive Substance
1997-10-20Original Approval
NICOTINE is FDA application ANDA074612, sponsored by DIFGEN PHARMS. Any recalls listed below come from FDA drug enforcement reports, and reaction counts are the number of FAERS adverse event reports that mention the drug and that reaction; a report does not prove the drug caused it.
Top Reported Reactions
1
DRUG INEFFECTIVE
1,764 reports
2
NAUSEA
1,096 reports
3
PRODUCT ADHESION ISSUE
929 reports
4
OVERDOSE
778 reports
5
HEADACHE
772 reports
6
NICOTINE DEPENDENCE
754 reports
7
FOETAL EXPOSURE DURING PREGNANCY
750 reports
8
TREATMENT NONCOMPLIANCE
683 reports
9
DYSPNOEA
655 reports
10
PAIN
630 reports