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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 124375583 | 12437558 | 3 | F | 20160701 | 20160606 | 20160708 | EXP | US-AMGEN-USASP2016070974 | AMGEN | 49.00 | YR | A | M | Y | 0.00000 | 20160708 | MD | 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 124375583 | 12437558 | 1 | PS | ARANESP | DARBEPOETIN ALFA | 1 | Unknown | UNK | 103951 | SOLUTION FOR INJECTION | |||||||||
| 124375583 | 12437558 | 2 | SS | ARANESP | DARBEPOETIN ALFA | 1 | Unknown | 500 MUG, Q3WK | 103951 | 500 | UG | SOLUTION FOR INJECTION | Q3W |
Indications of drugs used
| Event ID | CASEID | INDI DRUG SEQ | INDI PT |
|---|---|---|---|
| 124375583 | 12437558 | 1 | Anaemia |
Outcome of event
| Event ID | CASEID | OUTC COD |
|---|---|---|
| 124375583 | 12437558 | OT |
Reactions reported
| Event ID | CASEID | DRUG REC ACT | PT |
|---|---|---|---|
| 124375583 | 12437558 | Haemoglobin abnormal | |
| 124375583 | 12437558 | Therapy non-responder |
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 |
|---|---|---|---|---|---|---|
| 124375583 | 12437558 | 2 | 20160310 | 20160516 | 0 |