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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 8480326 | 8567783 | F | 8480326-5 | 20111101 | 20120622 | 20120630 | EXP | NL-AMGEN-NLDSP2012029777 | AMGENSAFETY | 69 | YR | M | Y | 20120630 | CN | NETHERLANDS |
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 |
|---|---|---|---|---|---|---|---|---|---|---|---|
| 8480326 | 1020135223 | PS | ENBREL | 1 | 50 MG, WEEKLY | ||||||
| 8480326 | 1020135224 | C | ASCAL /00002702/ | 2 | UNK |
Indications of drugs used
| Event ID | DRUG SEQ | INDI PT |
|---|---|---|
| 8480326 | 1020135223 | RHEUMATOID ARTHRITIS |
Outcome of event
| Event ID | OUTC COD |
|---|---|
| 8480326 | HO |
| 8480326 | DS |
| 8480326 | OT |
Reactions reported
| Event ID | PT |
|---|---|
| 8480326 | ARM AMPUTATION |
| 8480326 | EMBOLISM |
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 |
|---|---|---|---|---|---|
| 8480326 | 1020135223 | 20090101 |