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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
125322071 | 12532207 | 1 | I | 201508 | 20160624 | 20160706 | 20160706 | EXP | GB-MHRA-ADR 23524981 | GB-MYLANLABS-2016M1026786 | MYLAN | 0.00 | Y | 0.00000 | 20160706 | OT | GB | GB |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
125322071 | 12532207 | 1 | PS | FINASTERIDE. | FINASTERIDE | 1 | 1 MG, QD | N | U | 77578 | 1 | MG | QD | ||||||
125322071 | 12532207 | 2 | SS | FINASTERIDE. | FINASTERIDE | 1 | 1 MG, QD | N | U | 77578 | 1 | MG | QD |
Indications of drugs used
Event ID | CASEID | INDI DRUG SEQ | INDI PT |
---|---|---|---|
125322071 | 12532207 | 1 | Alopecia |
Outcome of event
Event ID | CASEID | OUTC COD |
---|---|---|
125322071 | 12532207 | DE |
125322071 | 12532207 | OT |
Reactions reported
Event ID | CASEID | DRUG REC ACT | PT |
---|---|---|---|
125322071 | 12532207 | Anxiety | |
125322071 | 12532207 | Completed suicide |
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 |
---|---|---|---|---|---|---|
125322071 | 12532207 | 1 | 2009 | 2011 | 0 | |
125322071 | 12532207 | 2 | 201404 | 201505 | 0 |