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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 90578307 | 9057830 | 7 | F | 2003 | 20160711 | 20130204 | 20160714 | EXP | US-009507513-1301USA013372 | MERCK | 0.00 | M | Y | 76.19000 | KG | 20160714 | 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 90578307 | 9057830 | 1 | PS | PROPECIA | FINASTERIDE | 1 | Oral | 1 MG, QD | 20788 | 1 | MG | FILM-COATED TABLET | QD | ||||||
| 90578307 | 9057830 | 2 | SS | PROPECIA | FINASTERIDE | 1 | Oral | 1 MG, QD | 20788 | 1 | MG | FILM-COATED TABLET | QD | ||||||
| 90578307 | 9057830 | 3 | SS | FINASTERIDE. | FINASTERIDE | 1 | Oral | 2.5 MG, QD | 20788 | 2.5 | MG | FILM-COATED TABLET | QD | ||||||
| 90578307 | 9057830 | 4 | SS | FINASTERIDE. | FINASTERIDE | 1 | Oral | 2.5 MG, QD | 1612 | MG | U | U | 0 | 2.5 | MG | TABLET | QD |
Indications of drugs used
| Event ID | CASEID | INDI DRUG SEQ | INDI PT |
|---|---|---|---|
| 90578307 | 9057830 | 1 | Alopecia |
| 90578307 | 9057830 | 3 | Alopecia |
| 90578307 | 9057830 | 4 | Alopecia |
Outcome of event
| Event ID | CASEID | OUTC COD |
|---|---|---|
| 90578307 | 9057830 | OT |
Reactions reported
| Event ID | CASEID | DRUG REC ACT | PT |
|---|---|---|---|
| 90578307 | 9057830 | Anorgasmia | |
| 90578307 | 9057830 | Back disorder | |
| 90578307 | 9057830 | Blood testosterone decreased | |
| 90578307 | 9057830 | Cognitive disorder | |
| 90578307 | 9057830 | Depression | |
| 90578307 | 9057830 | Disturbance in sexual arousal | |
| 90578307 | 9057830 | Erectile dysfunction | |
| 90578307 | 9057830 | Gastroenteritis | |
| 90578307 | 9057830 | Goitre | |
| 90578307 | 9057830 | Hyperthyroidism | |
| 90578307 | 9057830 | Intervertebral disc disorder | |
| 90578307 | 9057830 | Intervertebral disc operation | |
| 90578307 | 9057830 | Libido decreased | |
| 90578307 | 9057830 | Mole excision | |
| 90578307 | 9057830 | Muscle strain | |
| 90578307 | 9057830 | Myelopathy | |
| 90578307 | 9057830 | Overdose | |
| 90578307 | 9057830 | Scoliosis | |
| 90578307 | 9057830 | Semen volume decreased | |
| 90578307 | 9057830 | Sexual dysfunction | |
| 90578307 | 9057830 | Viral infection | |
| 90578307 | 9057830 | Wrong technique in product usage process |
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 |
|---|---|---|---|---|---|---|
| 90578307 | 9057830 | 1 | 20021002 | 20050201 | 0 | |
| 90578307 | 9057830 | 2 | 2005 | 200702 | 0 | |
| 90578307 | 9057830 | 3 | 2007 | 201101 | 0 | |
| 90578307 | 9057830 | 4 | 20090202 | 20101108 | 0 |