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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 126680061 | 12668006 | 1 | I | 20160804 | 20160819 | 20160819 | EXP | E2B_00586612 | CA-HQ SPECIALTY-CA-2016INT000797 | INTERCHEM | 60.00 | YR | F | Y | 0.00000 | 20160819 | 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 126680061 | 12668006 | 1 | PS | METHOTREXATE SODIUM. | METHOTREXATE SODIUM | 1 | Oral | UNK | U | 201749 | |||||||||
| 126680061 | 12668006 | 2 | SS | METHOTREXATE. | METHOTREXATE | 1 | Subcutaneous | UNK | U | 0 | |||||||||
| 126680061 | 12668006 | 3 | SS | ENBREL | ETANERCEPT | 1 | Unknown | UNK | U | 0 | |||||||||
| 126680061 | 12668006 | 4 | SS | PLAQUENIL | HYDROXYCHLOROQUINE SULFATE | 1 | Unknown | UNK | N | 0 | |||||||||
| 126680061 | 12668006 | 5 | SS | SIMPONI | GOLIMUMAB | 1 | Unknown | UNK | U | 0 | |||||||||
| 126680061 | 12668006 | 6 | SS | ACTEMRA | TOCILIZUMAB | 1 | Unknown | UNK | N | 0 | |||||||||
| 126680061 | 12668006 | 7 | SS | ARAVA | LEFLUNOMIDE | 1 | Unknown | 20 MG (20 MG,1 IN 1 D) | 0 | 20 | MG | ||||||||
| 126680061 | 12668006 | 8 | SS | PREDNISONE. | PREDNISONE | 1 | Unknown | 10 MG (10 MG,1 IN 1 D) | 0 | 10 | MG |
Indications of drugs used
| Event ID | CASEID | INDI DRUG SEQ | INDI PT |
|---|---|---|---|
| 126680061 | 12668006 | 1 | Rheumatoid arthritis |
| 126680061 | 12668006 | 2 | Rheumatoid arthritis |
| 126680061 | 12668006 | 3 | Rheumatoid arthritis |
| 126680061 | 12668006 | 4 | Rheumatoid arthritis |
| 126680061 | 12668006 | 5 | Rheumatoid arthritis |
| 126680061 | 12668006 | 6 | Rheumatoid arthritis |
| 126680061 | 12668006 | 7 | Rheumatoid arthritis |
| 126680061 | 12668006 | 8 | Rheumatoid arthritis |
Outcome of event
| Event ID | CASEID | OUTC COD |
|---|---|---|
| 126680061 | 12668006 | OT |
Reactions reported
| Event ID | CASEID | DRUG REC ACT | PT |
|---|---|---|---|
| 126680061 | 12668006 | Arthralgia | |
| 126680061 | 12668006 | Back injury | |
| 126680061 | 12668006 | Back pain | |
| 126680061 | 12668006 | Drug ineffective | |
| 126680061 | 12668006 | Intervertebral disc compression | |
| 126680061 | 12668006 | Intervertebral disc space narrowing | |
| 126680061 | 12668006 | Joint stiffness | |
| 126680061 | 12668006 | Joint swelling | |
| 126680061 | 12668006 | Local swelling | |
| 126680061 | 12668006 | Musculoskeletal stiffness | |
| 126680061 | 12668006 | Nausea | |
| 126680061 | 12668006 | Pain in extremity | |
| 126680061 | 12668006 | 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 |
|---|---|---|---|---|---|---|
| 126680061 | 12668006 | 6 | 201505 | 0 |