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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
125252751 | 12525275 | 1 | I | 2015 | 20160629 | 20160704 | 20160704 | EXP | ZA-AMGEN-ZAFSL2016086353 | AMGEN | 58.00 | YR | A | F | Y | 0.00000 | 20160704 | 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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
125252751 | 12525275 | 1 | PS | ARANESP | DARBEPOETIN ALFA | 1 | Subcutaneous | 40 UNK, QWK | U | 103951 | SOLUTION FOR INJECTION | /wk |
Indications of drugs used
Event ID | CASEID | INDI DRUG SEQ | INDI PT |
---|---|---|---|
125252751 | 12525275 | 1 | Product used for unknown indication |
Outcome of event
Event ID | CASEID | OUTC COD |
---|---|---|
125252751 | 12525275 | OT |
125252751 | 12525275 | DE |
Reactions reported
Event ID | CASEID | DRUG REC ACT | PT |
---|---|---|---|
125252751 | 12525275 | Fall | |
125252751 | 12525275 | Joint injury | |
125252751 | 12525275 | Sepsis | |
125252751 | 12525275 | Wound sepsis |
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 |
---|---|---|---|---|---|---|
125252751 | 12525275 | 1 | 201103 | 0 |