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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 4655343 | 5807769 | I | 4655343-3 | 20050120 | 20050331 | PER | UK108765 | AMGEN | F | N | 20050224 |
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 |
|---|---|---|---|---|---|---|---|---|---|---|---|
| 4655343 | 1005954370 | PS | NEULASTA | 1 | SUBCUTANEOUS | 6 MG, 1 IN 4 WEEKS, SC | U | U |
Indications of drugs used
| Event ID | DRUG SEQ | INDI PT |
|---|---|---|
| 4655343 | 1005954370 | CHEMOTHERAPY |
Outcome of event
| no results found |
Reactions reported
| Event ID | PT |
|---|---|
| 4655343 | MUSCULOSKELETAL PAIN |
Reporting Sources (this data is often not reported and may therefore be missing here)
| Event ID | RPSR COD |
|---|---|
| 4655343 | FGN |
| 4655343 | HP |
Therapies reported
| no results found |