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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
6028602 | 6877777 | I | 6028602-X | 20081231 | DIR | 56 | YR | M | N | 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 |
---|---|---|---|---|---|---|---|---|---|---|---|
6028602 | 1010954311 | PS | BUPROPION HCL | 1 | ORAL | 150 MG BID PO |
Indications of drugs used
Event ID | DRUG SEQ | INDI PT |
---|---|---|
6028602 | 1010954311 | SMOKING CESSATION THERAPY |
Outcome of event
Event ID | OUTC COD |
---|---|
6028602 | OT |
Reactions reported
Event ID | PT |
---|---|
6028602 | CONVULSION |
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 |
---|---|---|---|---|---|
6028602 | 1010954311 | 20071206 | 20071212 |