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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 126786862 | 12678686 | 2 | F | 20160823 | 20160823 | 20160830 | EXP | CA-AMGEN-CANSP2016107898 | AMGEN | 54.00 | YR | A | F | Y | 0.00000 | 20160830 | OT | 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 126786862 | 12678686 | 1 | PS | ENBREL | ETANERCEPT | 1 | Subcutaneous | UNK | U | 103795 | UNKNOWN FORMULATION | ||||||||
| 126786862 | 12678686 | 2 | SS | CELEBREX | CELECOXIB | 1 | Unknown | UNK | 0 | CAPSULE | |||||||||
| 126786862 | 12678686 | 3 | SS | HUMIRA | ADALIMUMAB | 1 | Subcutaneous | UNK | 0 | ||||||||||
| 126786862 | 12678686 | 4 | SS | LEFLUNOMIDE. | LEFLUNOMIDE | 1 | Unknown | UNK | 0 | ||||||||||
| 126786862 | 12678686 | 5 | SS | METHOTREXATE SODIUM. | METHOTREXATE SODIUM | 1 | Unknown | UNK | 0 | ||||||||||
| 126786862 | 12678686 | 6 | SS | RITUXAN | RITUXIMAB | 1 | Unknown | UNK | 0 | ||||||||||
| 126786862 | 12678686 | 7 | SS | SIMPONI | GOLIMUMAB | 1 | Subcutaneous | UNK | 0 | ||||||||||
| 126786862 | 12678686 | 8 | SS | VIOXX | ROFECOXIB | 1 | Unknown | UNK | 0 | TABLET | |||||||||
| 126786862 | 12678686 | 9 | SS | XELJANZ | TOFACITINIB CITRATE | 1 | Oral | 5 MG, BID | 0 | 5 | MG | BID | |||||||
| 126786862 | 12678686 | 10 | SS | XELJANZ | TOFACITINIB CITRATE | 1 | Oral | 10 MG, BID | 0 | 10 | MG | BID |
Indications of drugs used
| Event ID | CASEID | INDI DRUG SEQ | INDI PT |
|---|---|---|---|
| 126786862 | 12678686 | 1 | Rheumatoid arthritis |
| 126786862 | 12678686 | 2 | Rheumatoid arthritis |
| 126786862 | 12678686 | 3 | Rheumatoid arthritis |
| 126786862 | 12678686 | 4 | Product used for unknown indication |
| 126786862 | 12678686 | 5 | Rheumatoid arthritis |
| 126786862 | 12678686 | 6 | Rheumatoid arthritis |
| 126786862 | 12678686 | 7 | Rheumatoid arthritis |
| 126786862 | 12678686 | 8 | Rheumatoid arthritis |
| 126786862 | 12678686 | 9 | Rheumatoid arthritis |
Outcome of event
| Event ID | CASEID | OUTC COD |
|---|---|---|
| 126786862 | 12678686 | OT |
Reactions reported
| Event ID | CASEID | DRUG REC ACT | PT |
|---|---|---|---|
| 126786862 | 12678686 | Bone erosion | |
| 126786862 | 12678686 | Drug effect decreased | |
| 126786862 | 12678686 | Drug ineffective | |
| 126786862 | 12678686 | Nasopharyngitis | |
| 126786862 | 12678686 | Rheumatoid arthritis | |
| 126786862 | 12678686 | Stress |
Reporting Sources (this data is often not reported and may therefore be missing here)
| no results found |
Therapies reported
| no results found |