Person who experienced the adverse event (patient)
| Event ID | CASEID | CASEVERSION | I F COD | EVENT DT | MFR DT | INIT FDA DT | FDA DT | REPT COD | AUTH NUM | MFR NUM | MFR SNDR | LIT REF | AGE | AGE COD | AGE GRP | GNDR COD | E SUB | WT | WT COD | REPT DT | TO MFR | OCCP COD | REPORTER COUNTRY | OCCR COUNTRY |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 120009673 | 12000967 | 3 | F | 20050425 | 20160818 | 20160204 | 20160826 | EXP | CA-PFIZER INC-HQWYE695901JUN06 | PFIZER | 65.00 | YR | M | Y | 0.00000 | 20160826 | CN | CA | CA |
Drug(s) used by person
| Event ID | CASEID | DRUG SEQ | ROLE COD | DRUGNAME | PROD AI | VAL VBM | ROUTE | DOSE VBM | CUM DOSE CHR | CUM DOSE UNIT | DECHAL | RECHAL | LOT NUM | EXP DT | NDA NUM | DOSE AMT | DOSE UNIT | DOSE FORM | DOSE FREQ |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 120009673 | 12000967 | 1 | SS | ENBREL | ETANERCEPT | 1 | Subcutaneous | 25 MG, 2X/WK | U | 0 | 25 | MG | POWDER AND SOLVENT FOR SOLUTION FOR INJECTION | BIW | |||||
| 120009673 | 12000967 | 2 | PS | METHOTREXATE SODIUM. | METHOTREXATE SODIUM | 1 | UNK | 11719 | |||||||||||
| 120009673 | 12000967 | 3 | SS | CELEBREX | CELECOXIB | 1 | UNK | 20998 | CAPSULE, HARD | ||||||||||
| 120009673 | 12000967 | 4 | SS | HUMIRA | ADALIMUMAB | 1 | UNK | 0 | |||||||||||
| 120009673 | 12000967 | 5 | SS | ORENCIA | ABATACEPT | 1 | UNK | 0 | |||||||||||
| 120009673 | 12000967 | 6 | SS | PREDNISONE. | PREDNISONE | 1 | UNK | 0 | |||||||||||
| 120009673 | 12000967 | 7 | SS | PLAQUENIL | HYDROXYCHLOROQUINE SULFATE | 1 | UNK | 0 | TABLET |
Indications of drugs used
| Event ID | CASEID | INDI DRUG SEQ | INDI PT |
|---|---|---|---|
| 120009673 | 12000967 | 1 | Psoriatic arthropathy |
| 120009673 | 12000967 | 2 | Rheumatoid arthritis |
| 120009673 | 12000967 | 3 | Rheumatoid arthritis |
| 120009673 | 12000967 | 4 | Rheumatoid arthritis |
| 120009673 | 12000967 | 5 | Rheumatoid arthritis |
| 120009673 | 12000967 | 6 | Rheumatoid arthritis |
| 120009673 | 12000967 | 7 | Rheumatoid arthritis |
Outcome of event
| Event ID | CASEID | OUTC COD |
|---|---|---|
| 120009673 | 12000967 | OT |
Reactions reported
| Event ID | CASEID | DRUG REC ACT | PT |
|---|---|---|---|
| 120009673 | 12000967 | Condition aggravated | |
| 120009673 | 12000967 | Hypoaesthesia | |
| 120009673 | 12000967 | Multiple sclerosis | |
| 120009673 | 12000967 | Paraesthesia | |
| 120009673 | 12000967 | Rheumatoid arthritis |
Reporting Sources (this data is often not reported and may therefore be missing here)
| no results found |
Therapies reported
| Event ID | CASEID | DSG DRUG SEQ | START DT | END DT | DUR | DUR COD |
|---|---|---|---|---|---|---|
| 120009673 | 12000967 | 1 | 20050425 | 0 | ||
| 120009673 | 12000967 | 4 | 20160127 | 0 |