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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 6811417 | 7450030 | I | 6811417-X | 20100518 | 20100518 | 20100630 | PER | US-AMGEN-KDL413999 | AMGENSAFETY | YR | Y | 20100630 | 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|
| 6811417 | 1014011647 | PS | PROCRIT | 1 | SUBCUTANEOUS | NOT PROVIDED |
Indications of drugs used
| Event ID | DRUG SEQ | INDI PT |
|---|---|---|
| 6811417 | 1014011647 | DRUG USE FOR UNKNOWN INDICATION |
Outcome of event
| no results found |
Reactions reported
| Event ID | PT |
|---|---|
| 6811417 | MEDICAL DEVICE COMPLICATION |
Reporting Sources (this data is often not reported and may therefore be missing here)
| no results found |
Therapies reported
| no results found |