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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
125427121 | 12542712 | 1 | I | 20160406 | 20160704 | 20160709 | 20160709 | EXP | ZA-AMGEN-ZAFSL2016088305 | AMGEN | 77.00 | YR | E | M | Y | 0.00000 | 20160709 | CN | 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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
125427121 | 12542712 | 1 | PS | ARANESP | DARBEPOETIN ALFA | 1 | Subcutaneous | 80 MUG, Q2WK | 103951 | 80 | UG | SOLUTION FOR INJECTION IN PRE-FILLED SYRINGE | QOW |
Indications of drugs used
Event ID | CASEID | INDI DRUG SEQ | INDI PT |
---|---|---|---|
125427121 | 12542712 | 1 | Chronic kidney disease |
Outcome of event
Event ID | CASEID | OUTC COD |
---|---|---|
125427121 | 12542712 | HO |
125427121 | 12542712 | DE |
125427121 | 12542712 | OT |
Reactions reported
Event ID | CASEID | DRUG REC ACT | PT |
---|---|---|---|
125427121 | 12542712 | Coma | |
125427121 | 12542712 | Renal failure |
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 |
---|---|---|---|---|---|---|
125427121 | 12542712 | 1 | 201510 | 0 |