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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 125902991 | 12590299 | 1 | I | 201509 | 20141020 | 20160725 | 20160725 | EXP | CA-PFIZER INC-2015272227 | PFIZER | 47.00 | YR | F | Y | 0.00000 | 20160725 | 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 125902991 | 12590299 | 1 | SS | ENBREL | ETANERCEPT | 1 | Subcutaneous | UNK | Y | 0 | |||||||||
| 125902991 | 12590299 | 2 | PS | METHOTREXATE SODIUM. | METHOTREXATE SODIUM | 1 | Subcutaneous | 25 MG, UNK | 11719 | 25 | MG | SOLUTION FOR INJECTION | |||||||
| 125902991 | 12590299 | 3 | SS | XELJANZ | TOFACITINIB CITRATE | 1 | Oral | 5 MG, 2X/DAY | 203214 | 5 | MG | TABLET | BID | ||||||
| 125902991 | 12590299 | 4 | SS | XELJANZ | TOFACITINIB CITRATE | 1 | Oral | 10 MG, 2 EVERY DAY | 203214 | 10 | MG | TABLET | BID | ||||||
| 125902991 | 12590299 | 5 | SS | PREDNISONE. | PREDNISONE | 1 | Unknown | UNK | U | 0 | |||||||||
| 125902991 | 12590299 | 6 | SS | REMICADE | INFLIXIMAB | 1 | Intravenous (not otherwise specified) | UNK | U | 0 | POWDER AND SOLVENT FOR SOLUTION FOR INFUSION |
Indications of drugs used
| Event ID | CASEID | INDI DRUG SEQ | INDI PT |
|---|---|---|---|
| 125902991 | 12590299 | 1 | Rheumatoid arthritis |
| 125902991 | 12590299 | 2 | Rheumatoid arthritis |
| 125902991 | 12590299 | 3 | Rheumatoid arthritis |
| 125902991 | 12590299 | 5 | Rheumatoid arthritis |
| 125902991 | 12590299 | 6 | Rheumatoid arthritis |
Outcome of event
| Event ID | CASEID | OUTC COD |
|---|---|---|
| 125902991 | 12590299 | OT |
Reactions reported
| Event ID | CASEID | DRUG REC ACT | PT |
|---|---|---|---|
| 125902991 | 12590299 | Bone erosion | |
| 125902991 | 12590299 | Condition aggravated | |
| 125902991 | 12590299 | Drug ineffective | |
| 125902991 | 12590299 | Malaise | |
| 125902991 | 12590299 | Pain | |
| 125902991 | 12590299 | Rheumatoid arthritis | |
| 125902991 | 12590299 | Sensitivity to weather change | |
| 125902991 | 12590299 | Stress | |
| 125902991 | 12590299 | Swelling | |
| 125902991 | 12590299 | Weight decreased |
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 |
|---|---|---|---|---|---|---|
| 125902991 | 12590299 | 3 | 20141023 | 0 |