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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 109906246 | 10990624 | 6 | F | 2007 | 20160706 | 20150406 | 20160707 | PER | US-009507513-1504USA001251 | MERCK | 0.00 | M | Y | 0.00000 | 20160707 | LW | 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 109906246 | 10990624 | 1 | PS | PROPECIA | FINASTERIDE | 1 | Oral | UNK | 20788 | FILM-COATED TABLET | |||||||||
| 109906246 | 10990624 | 2 | SS | FINASTERIDE. | FINASTERIDE | 1 | Oral | 5 MG, UNK | 0 | 5 | MG | FILM-COATED TABLET |
Indications of drugs used
| Event ID | CASEID | INDI DRUG SEQ | INDI PT |
|---|---|---|---|
| 109906246 | 10990624 | 1 | Androgenetic alopecia |
| 109906246 | 10990624 | 2 | Androgenetic alopecia |
Outcome of event
| no results found |
Reactions reported
| Event ID | CASEID | DRUG REC ACT | PT |
|---|---|---|---|
| 109906246 | 10990624 | Drug administration error | |
| 109906246 | 10990624 | Erectile dysfunction | |
| 109906246 | 10990624 | Libido decreased | |
| 109906246 | 10990624 | Sexual dysfunction |
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 |
|---|---|---|---|---|---|---|
| 109906246 | 10990624 | 1 | 2009 | 0 | ||
| 109906246 | 10990624 | 2 | 2007 | 2012 | 0 |