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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 126222471 | 12622247 | 1 | I | 2010 | 20151210 | 20160804 | 20160804 | EXP | CA-PFIZER INC-2015444509 | PFIZER | 60.00 | YR | F | Y | 0.00000 | 20160804 | 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 126222471 | 12622247 | 1 | SS | ENBREL | ETANERCEPT | 1 | UNK | U | 0 | ||||||||||
| 126222471 | 12622247 | 2 | PS | METHOTREXATE SODIUM. | METHOTREXATE SODIUM | 1 | Oral | UNK | U | 11719 | |||||||||
| 126222471 | 12622247 | 3 | SS | METHOTREXATE SODIUM. | METHOTREXATE SODIUM | 1 | Subcutaneous | UNK | U | 11719 | |||||||||
| 126222471 | 12622247 | 4 | SS | PLAQUENIL | HYDROXYCHLOROQUINE SULFATE | 1 | UNK | N | 0 | TABLET | |||||||||
| 126222471 | 12622247 | 5 | SS | SIMPONI | GOLIMUMAB | 1 | UNK | U | 0 | ||||||||||
| 126222471 | 12622247 | 6 | SS | ACTEMRA | TOCILIZUMAB | 1 | UNK | N | 0 | ||||||||||
| 126222471 | 12622247 | 7 | SS | ARAVA | LEFLUNOMIDE | 1 | 20 MG, 1X/DAY | 0 | 20 | MG | QD | ||||||||
| 126222471 | 12622247 | 8 | SS | PREDNISONE. | PREDNISONE | 1 | 10 MG, 1X/DAY | 0 | 10 | MG | QD |
Indications of drugs used
| Event ID | CASEID | INDI DRUG SEQ | INDI PT |
|---|---|---|---|
| 126222471 | 12622247 | 1 | Rheumatoid arthritis |
| 126222471 | 12622247 | 2 | Rheumatoid arthritis |
| 126222471 | 12622247 | 4 | Rheumatoid arthritis |
| 126222471 | 12622247 | 5 | Rheumatoid arthritis |
| 126222471 | 12622247 | 6 | Rheumatoid arthritis |
| 126222471 | 12622247 | 7 | Rheumatoid arthritis |
| 126222471 | 12622247 | 8 | Rheumatoid arthritis |
Outcome of event
| Event ID | CASEID | OUTC COD |
|---|---|---|
| 126222471 | 12622247 | OT |
Reactions reported
| Event ID | CASEID | DRUG REC ACT | PT |
|---|---|---|---|
| 126222471 | 12622247 | Arthralgia | |
| 126222471 | 12622247 | Back injury | |
| 126222471 | 12622247 | Back pain | |
| 126222471 | 12622247 | Drug ineffective | |
| 126222471 | 12622247 | Intervertebral disc compression | |
| 126222471 | 12622247 | Intervertebral disc space narrowing | |
| 126222471 | 12622247 | Joint stiffness | |
| 126222471 | 12622247 | Joint swelling | |
| 126222471 | 12622247 | Local swelling | |
| 126222471 | 12622247 | Malaise | |
| 126222471 | 12622247 | Musculoskeletal pain | |
| 126222471 | 12622247 | Musculoskeletal stiffness | |
| 126222471 | 12622247 | Nausea | |
| 126222471 | 12622247 | Neck pain | |
| 126222471 | 12622247 | Pain | |
| 126222471 | 12622247 | Peripheral swelling |
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 |
|---|---|---|---|---|---|---|
| 126222471 | 12622247 | 6 | 201505 | 0 |