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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
127084381 | 12708438 | 1 | I | 20160829 | 20160901 | 20160901 | EXP | CA-GLAXOSMITHKLINE-CA2016GSK125597 | GLAXOSMITHKLINE | 76.00 | YR | M | Y | 0.00000 | 20160901 | PH | CA | CA |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
127084381 | 12708438 | 1 | PS | AVODART | DUTASTERIDE | 1 | 0.5 MG, 1D | U | 21319 | .5 | MG | CAPSULE | QD | ||||||
127084381 | 12708438 | 2 | SS | FLOMAX | TAMSULOSIN HYDROCHLORIDE | 1 | 0.4 MG, 1D | U | 0 | .4 | MG | TABLET | QD |
Indications of drugs used
Event ID | CASEID | INDI DRUG SEQ | INDI PT |
---|---|---|---|
127084381 | 12708438 | 1 | Benign prostatic hyperplasia |
127084381 | 12708438 | 2 | Product used for unknown indication |
Outcome of event
Event ID | CASEID | OUTC COD |
---|---|---|
127084381 | 12708438 | OT |
Reactions reported
Event ID | CASEID | DRUG REC ACT | PT |
---|---|---|---|
127084381 | 12708438 | Cardiac failure |
Reporting Sources (this data is often not reported and may therefore be missing here)
no results found |
Therapies reported
no results found |