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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
106545794 | 10654579 | 4 | F | 200806 | 20160815 | 20141216 | 20160823 | EXP | US-009507513-1110USA03607 | MERCK | 0.00 | M | Y | 73.16000 | KG | 20160823 | 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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
106545794 | 10654579 | 1 | PS | PROPECIA | FINASTERIDE | 1 | Oral | 1 MG, QD | 20788 | 1 | MG | FILM-COATED TABLET | QD | ||||||
106545794 | 10654579 | 2 | SS | PROSCAR | FINASTERIDE | 1 | Oral | 5 MG, QD | U | 0 | 5 | MG | FILM-COATED TABLET | QD | |||||
106545794 | 10654579 | 3 | SS | PROSCAR | FINASTERIDE | 1 | Oral | 4 MG, QD, CUT IN QUARTER, TAKE 1.25 MG DAILY | U | 0 | 4 | MG | FILM-COATED TABLET | QD | |||||
106545794 | 10654579 | 4 | SS | PROSCAR | FINASTERIDE | 1 | Oral | 1.25 MG DOSE(FREQ NOT SPECIFIED) | U | 0 | FILM-COATED TABLET | ||||||||
106545794 | 10654579 | 5 | SS | FINASTERIDE. | FINASTERIDE | 1 | Oral | 1.25 MG DOSE (FREQ NOT SPECIFIED) | U | U | 0 |
Indications of drugs used
Event ID | CASEID | INDI DRUG SEQ | INDI PT |
---|---|---|---|
106545794 | 10654579 | 1 | Androgenetic alopecia |
106545794 | 10654579 | 2 | Androgenetic alopecia |
106545794 | 10654579 | 5 | Androgenetic alopecia |
Outcome of event
Event ID | CASEID | OUTC COD |
---|---|---|
106545794 | 10654579 | DS |
106545794 | 10654579 | OT |
Reactions reported
Event ID | CASEID | DRUG REC ACT | PT |
---|---|---|---|
106545794 | 10654579 | Anxiety | |
106545794 | 10654579 | Benign prostatic hyperplasia | |
106545794 | 10654579 | Brain injury | |
106545794 | 10654579 | Cognitive disorder | |
106545794 | 10654579 | Depression | |
106545794 | 10654579 | Drug administration error | |
106545794 | 10654579 | Dysuria | |
106545794 | 10654579 | Ejaculation disorder | |
106545794 | 10654579 | Ejaculation failure | |
106545794 | 10654579 | Feeling abnormal | |
106545794 | 10654579 | Hypogonadism male | |
106545794 | 10654579 | Incorrect dose administered | |
106545794 | 10654579 | Insomnia | |
106545794 | 10654579 | Libido decreased | |
106545794 | 10654579 | Micturition urgency | |
106545794 | 10654579 | Muscle twitching | |
106545794 | 10654579 | Nocturia | |
106545794 | 10654579 | Organic erectile dysfunction | |
106545794 | 10654579 | Panic attack | |
106545794 | 10654579 | Paranoia | |
106545794 | 10654579 | Penis disorder | |
106545794 | 10654579 | Perineal pain | |
106545794 | 10654579 | Prostatic pain | |
106545794 | 10654579 | Prostatitis | |
106545794 | 10654579 | Rectal spasm | |
106545794 | 10654579 | Retrograde ejaculation | |
106545794 | 10654579 | Semen volume decreased | |
106545794 | 10654579 | Sexual dysfunction | |
106545794 | 10654579 | Testicular disorder | |
106545794 | 10654579 | Testicular pain | |
106545794 | 10654579 | Urinary retention | |
106545794 | 10654579 | Urinary tract obstruction | |
106545794 | 10654579 | 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 |
---|---|---|---|---|---|---|
106545794 | 10654579 | 1 | 20070219 | 20080725 | 0 | |
106545794 | 10654579 | 2 | 20080725 | 201010 | 0 | |
106545794 | 10654579 | 3 | 200806 | 20101009 | 0 | |
106545794 | 10654579 | 4 | 200803 | 20101009 | 0 | |
106545794 | 10654579 | 5 | 20080802 | 2008 | 0 |