MINI NICOTINE
Generic: NICOTINE POLACRILEX
P & L DevelopmentManufacturer
ORALRoute
NICOTINEActive Substance
2019-02-07Original Approval
MINI NICOTINE is FDA application ANDA207868, sponsored by PLD ACQUISITIONS. 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
1,400 reports
2
NAUSEA
700 reports
3
NICOTINE DEPENDENCE
608 reports
4
MACULAR DEGENERATION
567 reports
5
WRONG TECHNIQUE IN PRODUCT USAGE PROCESS
419 reports
6
ORAL DISCOMFORT
329 reports
7
DYSPEPSIA
314 reports
8
INTENTIONAL DRUG MISUSE
291 reports
9
MALAISE
286 reports
10
HEADACHE
239 reports