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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 121174765 | 12117476 | 5 | F | 201507 | 20160818 | 20160225 | 20160823 | EXP | CA-AMGEN-CANSP2016022145 | AMGEN | 69.00 | YR | E | F | Y | 0.00000 | 20160822 | 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 121174765 | 12117476 | 1 | PS | ENBREL | ETANERCEPT | 1 | Unknown | UNK | U | 103795 | UNKNOWN FORMULATION | ||||||||
| 121174765 | 12117476 | 2 | SS | METHOTREXATE SODIUM. | METHOTREXATE SODIUM | 1 | Unknown | 25 MG, QWK | 0 | 25 | MG | /wk | |||||||
| 121174765 | 12117476 | 3 | SS | XELJANZ | TOFACITINIB CITRATE | 1 | Oral | 5 MG, BID | 0 | 5 | MG | BID | |||||||
| 121174765 | 12117476 | 4 | SS | CELEBREX | CELECOXIB | 1 | Unknown | UNK | 0 | ||||||||||
| 121174765 | 12117476 | 5 | SS | PREDNISONE. | PREDNISONE | 1 | Unknown | UNK | 0 | ||||||||||
| 121174765 | 12117476 | 6 | C | FOLIC ACID. | FOLIC ACID | 1 | UNK | 0 | |||||||||||
| 121174765 | 12117476 | 7 | C | PLAQUENIL | HYDROXYCHLOROQUINE SULFATE | 1 | 200 MG, QD | 0 | 200 | MG | QD | ||||||||
| 121174765 | 12117476 | 8 | C | HYDROXYCHLOROQUINE | HYDROXYCHLOROQUINE | 1 | 200 MG/DAY | 0 | 200 | MG |
Indications of drugs used
| Event ID | CASEID | INDI DRUG SEQ | INDI PT |
|---|---|---|---|
| 121174765 | 12117476 | 1 | Rheumatoid arthritis |
| 121174765 | 12117476 | 2 | Rheumatoid arthritis |
| 121174765 | 12117476 | 3 | Rheumatoid arthritis |
| 121174765 | 12117476 | 4 | Product used for unknown indication |
| 121174765 | 12117476 | 5 | Product used for unknown indication |
| 121174765 | 12117476 | 7 | Rheumatoid arthritis |
Outcome of event
| Event ID | CASEID | OUTC COD |
|---|---|---|
| 121174765 | 12117476 | HO |
| 121174765 | 12117476 | OT |
Reactions reported
| Event ID | CASEID | DRUG REC ACT | PT |
|---|---|---|---|
| 121174765 | 12117476 | Ankle deformity | |
| 121174765 | 12117476 | Arthralgia | |
| 121174765 | 12117476 | Arthritis | |
| 121174765 | 12117476 | Condition aggravated | |
| 121174765 | 12117476 | Confusional state | |
| 121174765 | 12117476 | Cough | |
| 121174765 | 12117476 | Drug ineffective | |
| 121174765 | 12117476 | Fall | |
| 121174765 | 12117476 | Foot fracture | |
| 121174765 | 12117476 | Gait disturbance | |
| 121174765 | 12117476 | Hospitalisation | |
| 121174765 | 12117476 | Immobile | |
| 121174765 | 12117476 | Joint swelling | |
| 121174765 | 12117476 | Loss of consciousness | |
| 121174765 | 12117476 | Lower limb fracture | |
| 121174765 | 12117476 | Mouth ulceration | |
| 121174765 | 12117476 | Musculoskeletal discomfort | |
| 121174765 | 12117476 | Musculoskeletal stiffness | |
| 121174765 | 12117476 | Nausea | |
| 121174765 | 12117476 | Osteoporosis | |
| 121174765 | 12117476 | Pain | |
| 121174765 | 12117476 | Pain in extremity | |
| 121174765 | 12117476 | Rheumatoid arthritis | |
| 121174765 | 12117476 | Rhinorrhoea | |
| 121174765 | 12117476 | Spinal fracture |
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 |
|---|---|---|---|---|---|---|
| 121174765 | 12117476 | 1 | 201505 | 20160211 | 0 | |
| 121174765 | 12117476 | 3 | 20160412 | 0 | ||
| 121174765 | 12117476 | 8 | 2011 | 0 |