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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 6811162 | 7449783 | I | 6811162-0 | 20070101 | 20090728 | 20100630 | PER | US-AMGEN-KDL358202 | AMGENSAFETY | 70 | YR | F | Y | 54.5 | KG | 20100630 | 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|
| 6811162 | 1014010646 | PS | PROCRIT | 1 | SUBCUTANEOUS | NOT PROVIDED | |||||
| 6811162 | 1014010647 | C | IMURAN | 1 | |||||||
| 6811162 | 1014010648 | C | CYCLOSPORINE | 1 |
Indications of drugs used
| Event ID | DRUG SEQ | INDI PT |
|---|---|---|
| 6811162 | 1014010646 | RENAL FAILURE CHRONIC |
Outcome of event
| no results found |
Reactions reported
| Event ID | PT |
|---|---|
| 6811162 | FATIGUE |
| 6811162 | HAEMOGLOBIN DECREASED |
| 6811162 | LETHARGY |
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 |
|---|---|---|---|---|---|
| 6811162 | 1014010646 | 20060101 | |||
| 6811162 | 1014010647 | 19970101 | |||
| 6811162 | 1014010648 | 19970101 |