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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 6527777 | 7217352 | F | 2 | 6527777-3 | 20091104 | 20091221 | 20091231 | EXP | 8054510 | UCB, INC. | 35 | N | 60 | KG | 20091230 | SERBIA |
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 |
|---|---|---|---|---|---|---|---|---|---|---|---|
| 6527777 | 1012904016 | PS | CERTOLIZUMAB PEGOL (CERTOLIZUMAB PEGOL) | 2 | SUBCUTANEOUS | (200 MG 1X/2 WEEKS SUBCUTANEOUS), (400 MG QOD, - NR OF DOSES :31 SUBCUTANEOUS), ( 200 MG 1X/2 WEEKS, | Y |
Indications of drugs used
| Event ID | DRUG SEQ | INDI PT |
|---|---|---|
| 6527777 | 1012904016 | RHEUMATOID ARTHRITIS |
Outcome of event
| Event ID | OUTC COD |
|---|---|
| 6527777 | OT |
Reactions reported
| Event ID | PT |
|---|---|
| 6527777 | ESCHERICHIA URINARY TRACT INFECTION |
Reporting Sources (this data is often not reported and may therefore be missing here)
| Event ID | RPSR COD |
|---|---|
| 6527777 | FGN |
| 6527777 | HP |
| 6527777 | OTH |
| 6527777 | SDY |
Therapies reported
| Event ID | DRUG SEQ | START DT | END DT | DUR | DUR COD |
|---|---|---|---|---|---|
| 6527777 | 1012904016 | 20051228 | 20060612 | ||
| 6527777 | 1012904016 | 20060612 | 20071211 | ||
| 6527777 | 1012904016 | 20071225 | 20091110 | ||
| 6527777 | 1012904016 | 20091208 |