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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 126391201 | 12639120 | 1 | I | 20160728 | 20160803 | 20160810 | 20160810 | EXP | NL-AMGEN-NLDSL2016102050 | AMGEN | 80.00 | YR | E | M | Y | 0.00000 | 20160809 | CN | NL | NL |
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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 126391201 | 12639120 | 1 | PS | ARANESP | DARBEPOETIN ALFA | 1 | Subcutaneous | 500 MUG, Q3WK | U | 1056169 | 103951 | 500 | UG | SOLUTION FOR INJECTION IN PRE-FILLED SYRINGE | Q3W |
Indications of drugs used
| Event ID | CASEID | INDI DRUG SEQ | INDI PT |
|---|---|---|---|
| 126391201 | 12639120 | 1 | Myelodysplastic syndrome |
Outcome of event
| Event ID | CASEID | OUTC COD |
|---|---|---|
| 126391201 | 12639120 | OT |
| 126391201 | 12639120 | HO |
Reactions reported
| Event ID | CASEID | DRUG REC ACT | PT |
|---|---|---|---|
| 126391201 | 12639120 | Hospitalisation | |
| 126391201 | 12639120 | Off label use | |
| 126391201 | 12639120 | Pain |
Reporting Sources (this data is often not reported and may therefore be missing here)
| no results found |
Therapies reported
| no results found |