Person who experienced the adverse event (patient)
Event ID | CASEID | CASEVERSION | I F COD | EVENT DT | MFR DT | INIT FDA DT | FDA DT | REPT COD | AUTH NUM | MFR NUM | MFR SNDR | LIT REF | AGE | AGE COD | AGE GRP | GNDR COD | E SUB | WT | WT COD | REPT DT | TO MFR | OCCP COD | REPORTER COUNTRY | OCCR COUNTRY |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
125466631 | 12546663 | 1 | I | 20160704 | 20160708 | 20160711 | 20160711 | EXP | US-GLAXOSMITHKLINE-US2016098016 | GLAXOSMITHKLINE | 59.00 | YR | F | Y | 0.00000 | 20160711 | CN | US | US |
Drug(s) used by person
Event ID | CASEID | DRUG SEQ | ROLE COD | DRUGNAME | PROD AI | VAL VBM | ROUTE | DOSE VBM | CUM DOSE CHR | CUM DOSE UNIT | DECHAL | RECHAL | LOT NUM | EXP DT | NDA NUM | DOSE AMT | DOSE UNIT | DOSE FORM | DOSE FREQ |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
125466631 | 12546663 | 1 | PS | NICODERM CQ | NICOTINE | 1 | 21 MG, UNK | Y | 1514382 | 20165 | 21 | MG | TRANSDERMAL PATCH | ||||||
125466631 | 12546663 | 2 | SS | NICORETTE | NICOTINE | 1 | UNK | U | UNK | 0 | MEDICATED CHEWING-GUM |
Indications of drugs used
Event ID | CASEID | INDI DRUG SEQ | INDI PT |
---|---|---|---|
125466631 | 12546663 | 1 | Smoking cessation therapy |
125466631 | 12546663 | 2 | Smoking cessation therapy |
Outcome of event
no results found |
Reactions reported
Event ID | CASEID | DRUG REC ACT | PT |
---|---|---|---|
125466631 | 12546663 | Feeling abnormal | |
125466631 | 12546663 | Nausea | |
125466631 | 12546663 | Restlessness | |
125466631 | 12546663 | Withdrawal syndrome |
Reporting Sources (this data is often not reported and may therefore be missing here)
no results found |
Therapies reported
Event ID | CASEID | DSG DRUG SEQ | START DT | END DT | DUR | DUR COD |
---|---|---|---|---|---|---|
125466631 | 12546663 | 1 | 20160704 | 20160708 | 0 |