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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 5075639 | 6088291 | I | 5075639-3 | 20050311 | 20051208 | 20060809 | PER | US-AMGEN-US160629 | AMGEN | M | Y | 20060809 | OT | 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|
| 5075639 | 1007560433 | PS | EPOGEN | 1 | INTRAVENOUS | UNKNOWN |
Indications of drugs used
| Event ID | DRUG SEQ | INDI PT |
|---|---|---|
| 5075639 | 1007560433 | DIALYSIS |
Outcome of event
| no results found |
Reactions reported
| Event ID | PT |
|---|---|
| 5075639 | ABDOMINAL PAIN UPPER |
| 5075639 | DYSPNOEA |
| 5075639 | PRURITUS |
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 |
|---|---|---|---|---|---|
| 5075639 | 1007560433 | 20051122 |