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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 6474353 | 7217461 | I | 6474353-7 | 20090728 | 20090804 | 20091123 | PER | 8049868 | UCB, INC. | 45 | YR | F | N | 20091028 | MD | UNITED STATES |
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 |
|---|---|---|---|---|---|---|---|---|---|---|---|
| 6474353 | 1012713849 | PS | CIMZIA | 1 | SUBCUTANEOUS | 400 MG SC | D | D | |||
| 6474353 | 1012785480 | C | ZYRTEC | 1 | |||||||
| 6474353 | 1012785481 | C | NEXIUM | 1 | |||||||
| 6474353 | 1012785482 | C | CLARITIN | 1 | |||||||
| 6474353 | 1012785483 | C | METHOTREXATE | 1 | |||||||
| 6474353 | 1012785485 | C | VITAMIN D | 1 | |||||||
| 6474353 | 1012785486 | C | BACLOFEN | 1 | |||||||
| 6474353 | 1012785487 | C | HYDROCODONE | 2 | |||||||
| 6474353 | 1012785488 | C | GLUCOSAMINE | 2 | |||||||
| 6474353 | 1012785489 | C | SYNTHROID | 1 | |||||||
| 6474353 | 1012785490 | C | CYMBALTA | 1 | |||||||
| 6474353 | 1012785491 | C | ALPRAZOLAM | 1 | |||||||
| 6474353 | 1012785492 | C | TRIAMTERENE | 2 |
Indications of drugs used
| Event ID | DRUG SEQ | INDI PT |
|---|---|---|
| 6474353 | 1012713849 | RHEUMATOID ARTHRITIS |
Outcome of event
| no results found |
Reactions reported
| Event ID | PT |
|---|---|
| 6474353 | ARTHRALGIA |
| 6474353 | INFLUENZA LIKE ILLNESS |
Reporting Sources (this data is often not reported and may therefore be missing here)
| Event ID | RPSR COD |
|---|---|
| 6474353 | CR |
| 6474353 | HP |
Therapies reported
| Event ID | DRUG SEQ | START DT | END DT | DUR | DUR COD |
|---|---|---|---|---|---|
| 6474353 | 1012713849 | 20090728 |