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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
6028603 | 6877778 | I | 6028603-1 | 20080919 | 20081231 | DIR | 70 | YR | M | N | 68.9 | KG | 20081230 | 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 |
---|---|---|---|---|---|---|---|---|---|---|---|
6028603 | 1010954312 | PS | VARENICLINE | 2 | ORAL | 0.5 MG EVERY DAY PO | Y | D |
Indications of drugs used
Event ID | DRUG SEQ | INDI PT |
---|---|---|
6028603 | 1010954312 | SMOKING CESSATION THERAPY |
Outcome of event
no results found |
Reactions reported
Event ID | PT |
---|---|
6028603 | RASH |
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 |
---|---|---|---|---|---|
6028603 | 1010954312 | 20070718 | 20070919 |