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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 7076728 | 7934227 | I | 7076728-4 | 20101010 | 20101029 | DIR | 59 | YR | M | N | 20101015 | OT | 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|
| 7076728 | 1015020079 | PS | BUPROPION HCL | 1 | ORAL | 150MG DAILY PO | Y | Y |
Indications of drugs used
| Event ID | DRUG SEQ | INDI PT |
|---|---|---|
| 7076728 | 1015020079 | ANXIETY |
Outcome of event
| no results found |
Reactions reported
| Event ID | PT |
|---|---|
| 7076728 | ERECTILE DYSFUNCTION |
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 |
|---|---|---|---|---|---|
| 7076728 | 1015020079 | 20100501 | 20101001 |