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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 103553207 | 10355320 | 7 | F | 2014 | 20160809 | 20140731 | 20160822 | EXP | NZ-ABBVIE-14K-118-1263857-00 | ABBVIE | 0.00 | F | Y | 0.00000 | 20160822 | MD | COUNTRY NOT SPECIFIED | NZ |
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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 103553207 | 10355320 | 1 | PS | HUMIRA | ADALIMUMAB | 1 | Subcutaneous | UNKNOWN | 125057 | 40 | MG | SOLUTION FOR INJECTION | QOW | ||||||
| 103553207 | 10355320 | 2 | SS | ARAVA | LEFLUNOMIDE | 1 | Unknown | U | UNKNOWN | 0 | |||||||||
| 103553207 | 10355320 | 3 | SS | ARAVA | LEFLUNOMIDE | 1 | Unknown | U | UNKNOWN | 0 | |||||||||
| 103553207 | 10355320 | 4 | SS | METHOTREXATE. | METHOTREXATE | 1 | Unknown | U | UNKNOWN | 0 | |||||||||
| 103553207 | 10355320 | 5 | SS | METHOTREXATE. | METHOTREXATE | 1 | Unknown | U | UNKNOWN | 0 | |||||||||
| 103553207 | 10355320 | 6 | C | PREDNISONE. | PREDNISONE | 1 | 0 |
Indications of drugs used
| Event ID | CASEID | INDI DRUG SEQ | INDI PT |
|---|---|---|---|
| 103553207 | 10355320 | 1 | Rheumatoid arthritis |
| 103553207 | 10355320 | 2 | Product used for unknown indication |
| 103553207 | 10355320 | 4 | Product used for unknown indication |
| 103553207 | 10355320 | 6 | Product used for unknown indication |
Outcome of event
| Event ID | CASEID | OUTC COD |
|---|---|---|
| 103553207 | 10355320 | DS |
| 103553207 | 10355320 | OT |
Reactions reported
| Event ID | CASEID | DRUG REC ACT | PT |
|---|---|---|---|
| 103553207 | 10355320 | Acquired claw toe | |
| 103553207 | 10355320 | Arthralgia | |
| 103553207 | 10355320 | Drug ineffective | |
| 103553207 | 10355320 | Emotional disorder | |
| 103553207 | 10355320 | Fatigue | |
| 103553207 | 10355320 | Frustration tolerance decreased | |
| 103553207 | 10355320 | Joint contracture | |
| 103553207 | 10355320 | Musculoskeletal stiffness | |
| 103553207 | 10355320 | Pain | |
| 103553207 | 10355320 | Pain in extremity | |
| 103553207 | 10355320 | 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 |
|---|---|---|---|---|---|---|
| 103553207 | 10355320 | 1 | 201004 | 0 | ||
| 103553207 | 10355320 | 3 | 201405 | 0 | ||
| 103553207 | 10355320 | 5 | 201405 | 0 |