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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 5075124 | 6088461 | I | 5075124-9 | 20050101 | 20050919 | 20060809 | PER | US-AMGEN-US151087 | AMGEN | F | Y | 88.8 | KG | 20060809 | CN | 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|
| 5075124 | 1007558795 | PS | EPOGEN | 1 | NOT PROVIDED | ||||||
| 5075124 | 1007558796 | C | CALCITRIOL | 1 | |||||||
| 5075124 | 1007558797 | C | BLOOD CELLS, PACKED HUMAN | 2 |
Indications of drugs used
| Event ID | DRUG SEQ | INDI PT |
|---|---|---|
| 5075124 | 1007558795 | DIALYSIS |
Outcome of event
| Event ID | OUTC COD |
|---|---|
| 5075124 | HO |
Reactions reported
| Event ID | PT |
|---|---|
| 5075124 | HAEMOGLOBIN 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 |
|---|---|---|---|---|---|
| 5075124 | 1007558795 | 20041101 | |||
| 5075124 | 1007558796 | 20050901 | |||
| 5075124 | 1007558797 | 20050901 |