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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 5075640 | 6088290 | I | 5075640-X | 20051207 | 20051208 | 20060809 | PER | US-AMGEN-KDL161400 | AMGEN | F | Y | 86.3 | KG | 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|
| 5075640 | 1007560434 | PS | PROCRIT | 1 | NOT PROVIDED | ||||||
| 5075640 | 1007560435 | C | INSULIN | 1 | |||||||
| 5075640 | 1007560436 | C | TOPROL-XL | 1 |
Indications of drugs used
| Event ID | DRUG SEQ | INDI PT |
|---|---|---|
| 5075640 | 1007560434 | RENAL FAILURE CHRONIC |
Outcome of event
| no results found |
Reactions reported
| Event ID | PT |
|---|---|
| 5075640 | BLOOD GLUCOSE ABNORMAL |
| 5075640 | OEDEMA PERIPHERAL |
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 |
|---|---|---|---|---|---|
| 5075640 | 1007560434 | 20051120 | 20051207 |