Person who experienced the adverse event (patient)
| Event ID | CASEID | CASEVERSION | I F COD | EVENT DT | MFR DT | INIT FDA DT | FDA DT | REPT COD | AUTH NUM | MFR NUM | MFR SNDR | LIT REF | AGE | AGE COD | AGE GRP | GNDR COD | E SUB | WT | WT COD | REPT DT | TO MFR | OCCP COD | REPORTER COUNTRY | OCCR COUNTRY |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 89643682 | 8964368 | 2 | F | 20160804 | 20121214 | 20160822 | EXP | US-GLAXOSMITHKLINE-A0977163A | GLAXOSMITHKLINE | 0.00 | M | Y | 0.00000 | 20160822 | CN | US | US |
Drug(s) used by person
| Event ID | CASEID | DRUG SEQ | ROLE COD | DRUGNAME | PROD AI | VAL VBM | ROUTE | DOSE VBM | CUM DOSE CHR | CUM DOSE UNIT | DECHAL | RECHAL | LOT NUM | EXP DT | NDA NUM | DOSE AMT | DOSE UNIT | DOSE FORM | DOSE FREQ |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 89643682 | 8964368 | 1 | PS | AVODART | DUTASTERIDE | 1 | Oral | Y | 1ZP8476 | 21319 | 1 | DF | CAPSULE | QD | |||||
| 89643682 | 8964368 | 2 | SS | AVODART | DUTASTERIDE | 1 | 0.50 MG, QOD | Y | 21319 | .5 | MG | CAPSULE | QOD | ||||||
| 89643682 | 8964368 | 3 | C | ADVIL | IBUPROFEN | 1 | U | 0 |
Indications of drugs used
| Event ID | CASEID | INDI DRUG SEQ | INDI PT |
|---|---|---|---|
| 89643682 | 8964368 | 1 | Benign prostatic hyperplasia |
Outcome of event
| no results found |
Reactions reported
| Event ID | CASEID | DRUG REC ACT | PT |
|---|---|---|---|
| 89643682 | 8964368 | Alopecia | |
| 89643682 | 8964368 | Ejaculation disorder | |
| 89643682 | 8964368 | Erectile dysfunction | |
| 89643682 | 8964368 | Libido decreased |
Reporting Sources (this data is often not reported and may therefore be missing here)
| no results found |
Therapies reported
| Event ID | CASEID | DSG DRUG SEQ | START DT | END DT | DUR | DUR COD |
|---|---|---|---|---|---|---|
| 89643682 | 8964368 | 1 | 2009 | 0 | ||
| 89643682 | 8964368 | 2 | 2013 | 0 |