Person who experienced the adverse event (patient)
Event ID | CASE | I F COD | FOLL SEQ | IMAGE | EVENT DT | MFR DT | FDA DT | REPT COD | MFR NUM | MFR SNDR | AGE | AGE COD | GNDR COD | E SUB | WT | WT COD | REPT DT | OCCP COD | DEATH DT | TO MFR | CONFID | REPORTER COUNTRY |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
5117832 | 6123299 | F | 5117832-7 | 20060601 | 20060825 | 20060929 | EXP | US-AMGEN-US191526 | AMGEN | M | Y | 59 | KG | 20060929 | MD | UNITED STATES |
Drug(s) used by person
Event ID | DRUG SEQ | ROLE COD | DRUGNAME | VAL VBM | ROUTE | DOSE VBM | DECHAL | RECHAL | LOT NUM | EXP DT | NDA NUM |
---|---|---|---|---|---|---|---|---|---|---|---|
5117832 | 1007717869 | PS | PROCRIT | 1 | SUBCUTANEOUS | NOT PROVIDED | |||||
5117832 | 1007717870 | SS | ARANESP | 1 | SUBCUTANEOUS | NOT PROVIDED |
Indications of drugs used
Event ID | DRUG SEQ | INDI PT |
---|---|---|
5117832 | 1007717869 | RENAL FAILURE CHRONIC |
5117832 | 1007717870 | RENAL FAILURE CHRONIC |
Outcome of event
Event ID | OUTC COD |
---|---|
5117832 | HO |
5117832 | OT |
Reactions reported
Event ID | PT |
---|---|
5117832 | APLASIA PURE RED CELL |
5117832 | BONE MARROW FAILURE |
5117832 | CHEST PAIN |
5117832 | THERAPEUTIC RESPONSE DECREASED |
Reporting Sources (this data is often not reported and may therefore be missing here)
no results found |
Therapies reported
Event ID | DRUG SEQ | START DT | END DT | DUR | DUR COD |
---|---|---|---|---|---|
5117832 | 1007717869 | 20050503 | |||
5117832 | 1007717870 | 20040811 | 20060627 |