Person who experienced the adverse event (patient)
Event ID | CASE | I F COD | FOLL SEQ | IMAGE | EVENT DT | MFR DT | FDA DT | REPT COD | MFR NUM | MFR SNDR | AGE | AGE COD | GNDR COD | E SUB | WT | WT COD | REPT DT | OCCP COD | DEATH DT | TO MFR | CONFID | REPORTER COUNTRY |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
6142813 | 7202801 | I | 6142813-4 | 20070709 | 20090402 | DIR | 62 | YR | M | N | 96.62 | KG | PH | N | Y | UNITED STATES |
Drug(s) used by person
Event ID | DRUG SEQ | ROLE COD | DRUGNAME | VAL VBM | ROUTE | DOSE VBM | DECHAL | RECHAL | LOT NUM | EXP DT | NDA NUM |
---|---|---|---|---|---|---|---|---|---|---|---|
6142813 | 1011376402 | PS | VARENICLINE | 2 | ORAL | 1 TAB EVERY DAY PO | Y |
Indications of drugs used
Event ID | DRUG SEQ | INDI PT |
---|---|---|
6142813 | 1011376402 | SMOKING CESSATION THERAPY |
Outcome of event
no results found |
Reactions reported
Event ID | PT |
---|---|
6142813 | DIARRHOEA |
6142813 | DYSPNOEA |
6142813 | NAUSEA |
6142813 | VOMITING |
Reporting Sources (this data is often not reported and may therefore be missing here)
no results found |
Therapies reported
Event ID | DRUG SEQ | START DT | END DT | DUR | DUR COD |
---|---|---|---|---|---|
6142813 | 1011376402 | 20070706 | 20070709 |