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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 8480330 | 8536263 | F | 8480330-7 | 20110422 | 20120625 | 20120630 | EXP | KR-TEVA-334403ISR | TEVA | 60 | YR | M | Y | 20120630 | MD | KOREA, REPUBLIC OF |
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 |
|---|---|---|---|---|---|---|---|---|---|---|---|
| 8480330 | 1020135232 | C | CELECOXIB | 1 | |||||||
| 8480330 | 1020135231 | SS | ABATACEPT | 2 | INTRAVENOUS | ||||||
| 8480330 | 1020135233 | C | PREDNISOLONE | 1 | |||||||
| 8480330 | 1020135234 | C | FOLIC ACID | 1 | |||||||
| 8480330 | 1020135230 | PS | METHOTREXATE | 1 | 081099 | ||||||
| 8480330 | 1020135235 | C | CIMETIDINE | 1 |
Indications of drugs used
| Event ID | DRUG SEQ | INDI PT |
|---|---|---|
| 8480330 | 1020135231 | RHEUMATOID ARTHRITIS |
| 8480330 | 1020135230 | RHEUMATOID ARTHRITIS |
Outcome of event
| Event ID | OUTC COD |
|---|---|
| 8480330 | OT |
Reactions reported
| Event ID | PT |
|---|---|
| 8480330 | LYMPH NODE TUBERCULOSIS |
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 |
|---|---|---|---|---|---|
| 8480330 | 1020135232 | 20060125 | |||
| 8480330 | 1020135231 | 20070801 | 20110607 | ||
| 8480330 | 1020135233 | 20060125 | |||
| 8480330 | 1020135234 | 20110125 | |||
| 8480330 | 1020135230 | 20060125 | |||
| 8480330 | 1020135235 | 20110125 |