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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 87403614 | 8740361 | 4 | F | 201009 | 20160711 | 20120823 | 20160714 | PER | US-009507513-1208USA003683 | MERCK | 0.00 | M | Y | 84.35000 | KG | 20160714 | MD | 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 87403614 | 8740361 | 1 | PS | PROPECIA | FINASTERIDE | 1 | Oral | 1 MG, QD | U | 20788 | 1 | MG | FILM-COATED TABLET | QD | |||||
| 87403614 | 8740361 | 2 | C | ALBUTEROL. | ALBUTEROL | 1 | UNK | U | 0 |
Indications of drugs used
| Event ID | CASEID | INDI DRUG SEQ | INDI PT |
|---|---|---|---|
| 87403614 | 8740361 | 1 | Alopecia |
| 87403614 | 8740361 | 2 | Asthma |
Outcome of event
| no results found |
Reactions reported
| Event ID | CASEID | DRUG REC ACT | PT |
|---|---|---|---|
| 87403614 | 8740361 | Cognitive disorder | |
| 87403614 | 8740361 | Dermatitis | |
| 87403614 | 8740361 | Erectile dysfunction | |
| 87403614 | 8740361 | Hair transplant | |
| 87403614 | 8740361 | 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 |
|---|---|---|---|---|---|---|
| 87403614 | 8740361 | 1 | 20100607 | 20100910 | 0 | |
| 87403614 | 8740361 | 2 | 1993 | 0 |