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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
124747092 | 12474709 | 2 | F | 20160803 | 20160617 | 20160811 | EXP | GB-AMGEN-GBRSL2016075071 | AMGEN | 53.00 | YR | A | M | Y | 0.00000 | 20160811 | OT | GB | GB |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
124747092 | 12474709 | 1 | PS | ARANESP | DARBEPOETIN ALFA | 1 | Unknown | 30 MUG, UNK | U | 103951 | 30 | UG | SOLUTION FOR INJECTION IN PRE-FILLED SYRINGE |
Indications of drugs used
Event ID | CASEID | INDI DRUG SEQ | INDI PT |
---|---|---|---|
124747092 | 12474709 | 1 | Product used for unknown indication |
Outcome of event
Event ID | CASEID | OUTC COD |
---|---|---|
124747092 | 12474709 | HO |
124747092 | 12474709 | OT |
Reactions reported
Event ID | CASEID | DRUG REC ACT | PT |
---|---|---|---|
124747092 | 12474709 | Dialysis | |
124747092 | 12474709 | Dizziness | |
124747092 | 12474709 | Fall | |
124747092 | 12474709 | Hypertension | |
124747092 | 12474709 | Renal disorder |
Reporting Sources (this data is often not reported and may therefore be missing here)
no results found |
Therapies reported
no results found |