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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
125989491 | 12598949 | 1 | I | 20160311 | 20160721 | 20160726 | 20160726 | EXP | ZA-AMGEN-ZAFSL2016096177 | AMGEN | 58.00 | YR | A | F | Y | 0.00000 | 20160726 | OT | ZA | ZA |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
125989491 | 12598949 | 1 | PS | ARANESP | DARBEPOETIN ALFA | 1 | Subcutaneous | 30 MUG, Q2WK | 103951 | 30 | UG | SOLUTION FOR INJECTION IN PRE-FILLED SYRINGE | QOW |
Indications of drugs used
Event ID | CASEID | INDI DRUG SEQ | INDI PT |
---|---|---|---|
125989491 | 12598949 | 1 | Nephrogenic anaemia |
Outcome of event
Event ID | CASEID | OUTC COD |
---|---|---|
125989491 | 12598949 | DE |
125989491 | 12598949 | OT |
Reactions reported
Event ID | CASEID | DRUG REC ACT | PT |
---|---|---|---|
125989491 | 12598949 | Death | |
125989491 | 12598949 | Haemoglobin abnormal | |
125989491 | 12598949 | Hypotension |
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 |
---|---|---|---|---|---|---|
125989491 | 12598949 | 1 | 20150414 | 0 |