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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
125310091 | 12531009 | 1 | I | 201601 | 20160630 | 20160706 | 20160706 | EXP | ZA-AMGEN-ZAFSL2016087080 | AMGEN | 47.00 | YR | A | F | Y | 0.00000 | 20160706 | 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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
125310091 | 12531009 | 1 | PS | ARANESP | DARBEPOETIN ALFA | 1 | Subcutaneous | 30 UNK, Q2WK | 103951 | SOLUTION FOR INJECTION | QOW |
Indications of drugs used
Event ID | CASEID | INDI DRUG SEQ | INDI PT |
---|---|---|---|
125310091 | 12531009 | 1 | Nephrogenic anaemia |
Outcome of event
Event ID | CASEID | OUTC COD |
---|---|---|
125310091 | 12531009 | DE |
Reactions reported
Event ID | CASEID | DRUG REC ACT | PT |
---|---|---|---|
125310091 | 12531009 | Death | |
125310091 | 12531009 | Haemoglobin abnormal |
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 |
---|---|---|---|---|---|---|
125310091 | 12531009 | 1 | 201508 | 0 |