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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
6142796 | 7202767 | I | 6142796-7 | 20071008 | 20090402 | DIR | 50 | YR | F | N | 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 |
---|---|---|---|---|---|---|---|---|---|---|---|
6142796 | 1011376330 | PS | VARENICLINE | 2 | ORAL | 1 MG BID PO | Y |
Indications of drugs used
Event ID | DRUG SEQ | INDI PT |
---|---|---|
6142796 | 1011376330 | SMOKING CESSATION THERAPY |
Outcome of event
no results found |
Reactions reported
Event ID | PT |
---|---|
6142796 | CONSTIPATION |
6142796 | HEADACHE |
6142796 | NAUSEA |
6142796 | 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 |
---|---|---|---|---|---|
6142796 | 1011376330 | 20070808 | 20071001 |