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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 6527775 | 7014375 | F | 2 | 6527775-X | 20080504 | 20091218 | 20091231 | EXP | 8033874 | UCB. INC. | 80 | F | N | 55 | KG | 20091230 | CZECH REPUBLIC |
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 |
|---|---|---|---|---|---|---|---|---|---|---|---|
| 6527775 | 1012904014 | PS | CERTOLIZUMAB PEGOL (CDP870) | 2 | SUBCUTANEOUS | (400 MG, ONCE MONTHLY SUBCUTANEOUS), (400 MG , DOSE FREQ. : ONCE MONTHLY SUBCUTANEOUS) | Y |
Indications of drugs used
| Event ID | DRUG SEQ | INDI PT |
|---|---|---|
| 6527775 | 1012904014 | RHEUMATOID ARTHRITIS |
Outcome of event
| Event ID | OUTC COD |
|---|---|
| 6527775 | HO |
Reactions reported
| Event ID | PT |
|---|---|
| 6527775 | BLOOD CREATININE INCREASED |
| 6527775 | CALCULUS URETERIC |
| 6527775 | CULTURE URINE POSITIVE |
| 6527775 | ESCHERICHIA URINARY TRACT INFECTION |
| 6527775 | HYDRONEPHROSIS |
| 6527775 | PYELONEPHRITIS |
Reporting Sources (this data is often not reported and may therefore be missing here)
| Event ID | RPSR COD |
|---|---|
| 6527775 | FGN |
| 6527775 | HP |
| 6527775 | SDY |
Therapies reported
| Event ID | DRUG SEQ | START DT | END DT | DUR | DUR COD |
|---|---|---|---|---|---|
| 6527775 | 1012904014 | 20040602 | 20080519 | ||
| 6527775 | 1012904014 | 20031016 |