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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
110473113 | 11047311 | 3 | F | 2004 | 20160628 | 20150420 | 20160701 | PER | US-009507513-1504USA017805 | MERCK | 0.00 | M | Y | 0.00000 | 20160701 | 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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
110473113 | 11047311 | 1 | PS | PROPECIA | FINASTERIDE | 1 | Oral | 1 MG, UNKNOWN | 20788 | 1 | MG | FILM-COATED TABLET | |||||||
110473113 | 11047311 | 2 | SS | FINASTERIDE. | FINASTERIDE | 1 | Oral | 1 MG, UNKNOWN | 20788 | 1 | MG | FILM-COATED TABLET |
Indications of drugs used
Event ID | CASEID | INDI DRUG SEQ | INDI PT |
---|---|---|---|
110473113 | 11047311 | 1 | Alopecia |
110473113 | 11047311 | 2 | Alopecia |
Outcome of event
no results found |
Reactions reported
Event ID | CASEID | DRUG REC ACT | PT |
---|---|---|---|
110473113 | 11047311 | Erectile dysfunction | |
110473113 | 11047311 | Hypercholesterolaemia | |
110473113 | 11047311 | Hyperglycaemia | |
110473113 | 11047311 | Loss of libido | |
110473113 | 11047311 | Myalgia | |
110473113 | 11047311 | Overweight | |
110473113 | 11047311 | 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 |
---|---|---|---|---|---|---|
110473113 | 11047311 | 1 | 20030312 | 0 | ||
110473113 | 11047311 | 2 | 2009 | 0 |