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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 125490021 | 12549002 | 1 | I | 20160630 | 20160712 | 20160712 | EXP | CA-ABBVIE-16K-028-1667201-00 | ABBVIE | 0.00 | F | Y | 0.00000 | 20160712 | 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 125490021 | 12549002 | 1 | PS | HUMIRA | ADALIMUMAB | 1 | Subcutaneous | UNKNOWN | 125057 | 40 | MG | SOLUTION FOR INJECTION | /wk | ||||||
| 125490021 | 12549002 | 2 | SS | ARTHROTEC | DICLOFENAC SODIUMMISOPROSTOL | 1 | Oral | UNKNOWN | 0 | 75 | MG | ||||||||
| 125490021 | 12549002 | 3 | SS | ACTEMRA | TOCILIZUMAB | 1 | Unknown | UNKNOWN | 0 | ||||||||||
| 125490021 | 12549002 | 4 | SS | ORENCIA | ABATACEPT | 1 | Unknown | UNKNOWN | 0 | ||||||||||
| 125490021 | 12549002 | 5 | SS | CIMZIA | CERTOLIZUMAB PEGOL | 1 | Unknown | UNKNOWN | 0 | ||||||||||
| 125490021 | 12549002 | 6 | SS | RITUXAN | RITUXIMAB | 1 | Unknown | UNKNOWN | 0 | ||||||||||
| 125490021 | 12549002 | 7 | C | METHOTREXATE. | METHOTREXATE | 1 | Subcutaneous | 0 | 20 | MG | /wk | ||||||||
| 125490021 | 12549002 | 8 | C | METHOTREXATE. | METHOTREXATE | 1 | Oral | 0 | 25 | MG | /wk |
Indications of drugs used
| Event ID | CASEID | INDI DRUG SEQ | INDI PT |
|---|---|---|---|
| 125490021 | 12549002 | 1 | Product used for unknown indication |
| 125490021 | 12549002 | 2 | Product used for unknown indication |
| 125490021 | 12549002 | 3 | Rheumatoid arthritis |
| 125490021 | 12549002 | 4 | Rheumatoid arthritis |
| 125490021 | 12549002 | 5 | Rheumatoid arthritis |
| 125490021 | 12549002 | 6 | Rheumatoid arthritis |
| 125490021 | 12549002 | 7 | Product used for unknown indication |
Outcome of event
| Event ID | CASEID | OUTC COD |
|---|---|---|
| 125490021 | 12549002 | OT |
Reactions reported
| Event ID | CASEID | DRUG REC ACT | PT |
|---|---|---|---|
| 125490021 | 12549002 | Drug ineffective | |
| 125490021 | 12549002 | 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 |
|---|---|---|---|---|---|---|
| 125490021 | 12549002 | 1 | 201106 | 201109 | 0 | |
| 125490021 | 12549002 | 7 | 2009 | 201503 | 0 | |
| 125490021 | 12549002 | 8 | 201503 | 0 |