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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 6811163 | 7449784 | I | 6811163-2 | 20090731 | 20100630 | PER | US-AMGEN-KDL358344 | AMGENSAFETY | YR | F | Y | 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|
| 6811163 | 1014010649 | PS | EPOGEN | 1 | UNKNOWN | ||||||
| 6811163 | 1014010650 | C | ANTIDEPRESSANT NOS | 2 |
Indications of drugs used
| Event ID | DRUG SEQ | INDI PT |
|---|---|---|
| 6811163 | 1014010649 | DRUG USE FOR UNKNOWN INDICATION |
Outcome of event
| no results found |
Reactions reported
| Event ID | PT |
|---|---|
| 6811163 | FATIGUE |
| 6811163 | MALAISE |
Reporting Sources (this data is often not reported and may therefore be missing here)
| no results found |
Therapies reported
| no results found |