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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 106637033 | 10663703 | 3 | F | 2014 | 20160722 | 20141219 | 20160727 | EXP | BR-AMGEN-BRASP2014098285 | AMGEN | 42.00 | YR | A | F | Y | 75.00000 | KG | 20160727 | CN | BR | BR |
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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 106637033 | 10663703 | 1 | PS | ENBREL | ETANERCEPT | 1 | Subcutaneous | 50 MG, WEEKLY | 103795 | 50 | MG | SOLUTION FOR INJECTION IN PRE-FILLED SYRINGE | /wk | ||||||
| 106637033 | 10663703 | 2 | SS | ARAVA | LEFLUNOMIDE | 1 | Unknown | UNK | 0 | ||||||||||
| 106637033 | 10663703 | 3 | C | METHOTREXATE. | METHOTREXATE | 1 | UNK, WEEKLY | 0 | /wk | ||||||||||
| 106637033 | 10663703 | 4 | C | METHOTREXATE. | METHOTREXATE | 1 | 3 ^CP^ PER WEEK | 0 | 3 | DF | /wk | ||||||||
| 106637033 | 10663703 | 5 | C | FOLIC ACID. | FOLIC ACID | 1 | UNK, WEEKLY | 0 | /wk | ||||||||||
| 106637033 | 10663703 | 6 | C | FOLIC ACID. | FOLIC ACID | 1 | UNK, WEEKLY | 0 | /wk | ||||||||||
| 106637033 | 10663703 | 7 | C | TRAMAL | TRAMADOL | 1 | 50 UNK, 3X/DAY | 0 | TID | ||||||||||
| 106637033 | 10663703 | 8 | C | PREDNISONE. | PREDNISONE | 1 | 5 MG, UNK | 0 | 5 | MG | |||||||||
| 106637033 | 10663703 | 9 | C | PREDNISONE. | PREDNISONE | 1 | 5 MG, UNK | 0 | 5 | MG |
Indications of drugs used
| Event ID | CASEID | INDI DRUG SEQ | INDI PT |
|---|---|---|---|
| 106637033 | 10663703 | 1 | Juvenile idiopathic arthritis |
| 106637033 | 10663703 | 2 | Product used for unknown indication |
Outcome of event
| Event ID | CASEID | OUTC COD |
|---|---|---|
| 106637033 | 10663703 | OT |
Reactions reported
| Event ID | CASEID | DRUG REC ACT | PT |
|---|---|---|---|
| 106637033 | 10663703 | Cholelithiasis | |
| 106637033 | 10663703 | Condition aggravated | |
| 106637033 | 10663703 | Injection site erythema | |
| 106637033 | 10663703 | Juvenile idiopathic arthritis | |
| 106637033 | 10663703 | Malaise | |
| 106637033 | 10663703 | Tachycardia |
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 |
|---|---|---|---|---|---|---|
| 106637033 | 10663703 | 1 | 20141003 | 2015 | 0 |