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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 126262481 | 12626248 | 1 | I | 20160721 | 20160805 | 20160805 | EXP | E2B_00566329 | CA-HQ SPECIALTY-CA-2016INT000677 | INTERCHEM | 0.00 | F | Y | 0.00000 | 20160805 | MD | 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 126262481 | 12626248 | 1 | PS | METHOTREXATE SODIUM. | METHOTREXATE SODIUM | 1 | 2.8571 MG (20 MG, 1 IN 1 W) | U | 201749 | 20 | MG | ||||||||
| 126262481 | 12626248 | 2 | SS | ENBREL | ETANERCEPT | 1 | UNK | U | 0 | ||||||||||
| 126262481 | 12626248 | 3 | SS | HUMIRA | ADALIMUMAB | 1 | Subcutaneous | UNK | U | 0 | |||||||||
| 126262481 | 12626248 | 4 | SS | LEFLUNOMIDE. | LEFLUNOMIDE | 1 | UNK, DAILY | U | 0 | ||||||||||
| 126262481 | 12626248 | 5 | SS | ORENCIA | ABATACEPT | 1 | UNK | U | 0 | ||||||||||
| 126262481 | 12626248 | 6 | SS | PLAQUENIL /00072602/ | HYDROXYCHLOROQUINE DIPHOSPHATE | 1 | 400 MG, 1 D | U | 0 | 400 | MG |
Indications of drugs used
| Event ID | CASEID | INDI DRUG SEQ | INDI PT |
|---|---|---|---|
| 126262481 | 12626248 | 1 | Product used for unknown indication |
| 126262481 | 12626248 | 2 | Product used for unknown indication |
| 126262481 | 12626248 | 3 | Rheumatoid arthritis |
| 126262481 | 12626248 | 4 | Product used for unknown indication |
| 126262481 | 12626248 | 5 | Product used for unknown indication |
| 126262481 | 12626248 | 6 | Product used for unknown indication |
Outcome of event
| Event ID | CASEID | OUTC COD |
|---|---|---|
| 126262481 | 12626248 | OT |
Reactions reported
| Event ID | CASEID | DRUG REC ACT | PT |
|---|---|---|---|
| 126262481 | 12626248 | Activities of daily living impaired | |
| 126262481 | 12626248 | Bone erosion | |
| 126262481 | 12626248 | Drug hypersensitivity | |
| 126262481 | 12626248 | Drug ineffective | |
| 126262481 | 12626248 | Drug intolerance | |
| 126262481 | 12626248 | Gastric ulcer | |
| 126262481 | 12626248 | Inflammation | |
| 126262481 | 12626248 | Pain | |
| 126262481 | 12626248 | Rheumatoid factor positive | |
| 126262481 | 12626248 | Synovitis |
Reporting Sources (this data is often not reported and may therefore be missing here)
| no results found |
Therapies reported
| no results found |