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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 6526949 | 7614073 | I | 6526949-1 | 20090921 | 20100104 | DIR | 66 | YR | M | N | 226 | LBS | 20091223 | CN | N | N | 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|
| 6526949 | 1012900367 | PS | FINASTERIDE | 1 | ORAL | 5MG TAB 1 TAB ORAL | Y | D |
Indications of drugs used
| Event ID | DRUG SEQ | INDI PT |
|---|---|---|
| 6526949 | 1012900367 | PROSTATOMEGALY |
Outcome of event
| Event ID | OUTC COD |
|---|---|
| 6526949 | OT |
Reactions reported
| Event ID | PT |
|---|---|
| 6526949 | MUSCLE TIGHTNESS |
| 6526949 | PRODUCT SUBSTITUTION ISSUE |
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 |
|---|---|---|---|---|---|
| 6526949 | 1012900367 | 20090909 |