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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 6139045 | 6957267 | I | 6139045-2 | 20041201 | 20090326 | 20090331 | EXP | FR-AMGEN-UK334626 | AMGENSAFETY | 9 | F | Y | 59 | KG | 20090331 | MD | FRANCE |
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 |
|---|---|---|---|---|---|---|---|---|---|---|---|
| 6139045 | 1011360427 | PS | KINERET | 1 | UNKNOWN | UNKNOWN | |||||
| 6139045 | 1011360428 | SS | CORTANCYL | 2 | |||||||
| 6139045 | 1011360429 | C | UNSPECIFIED GROWTH HORMONE | 2 |
Indications of drugs used
| Event ID | DRUG SEQ | INDI PT |
|---|---|---|
| 6139045 | 1011360427 | JUVENILE ARTHRITIS |
Outcome of event
| Event ID | OUTC COD |
|---|---|
| 6139045 | DS |
| 6139045 | OT |
Reactions reported
| Event ID | PT |
|---|---|
| 6139045 | CATARACT |
| 6139045 | HYPERMETROPIA |
| 6139045 | INFLAMMATION |
| 6139045 | INJECTION SITE ERYTHEMA |
| 6139045 | INJECTION SITE PAIN |
| 6139045 | LIPOATROPHY |
| 6139045 | SKIN CHAPPED |
| 6139045 | VISUAL ACUITY REDUCED TRANSIENTLY |
| 6139045 | VISUAL FIELD DEFECT |
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 |
|---|---|---|---|---|---|
| 6139045 | 1011360427 | 20041117 |