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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 126252741 | 12625274 | 1 | I | 20160728 | 20160805 | 20160805 | EXP | CA-AMGEN-CANSP2016100343 | AMGEN | 71.00 | YR | E | F | Y | 0.00000 | 20160805 | 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 126252741 | 12625274 | 1 | PS | ENBREL | ETANERCEPT | 1 | Unknown | UNK | U | 103795 | UNKNOWN FORMULATION | ||||||||
| 126252741 | 12625274 | 2 | SS | GOLD | GOLD | 1 | Unknown | UNK | 0 | ||||||||||
| 126252741 | 12625274 | 3 | SS | LEFLUNOMIDE. | LEFLUNOMIDE | 1 | Unknown | 20 MG, QD | 0 | 20 | MG | QD | |||||||
| 126252741 | 12625274 | 4 | SS | SULFASALAZINE. | SULFASALAZINE | 1 | Unknown | 1 G, BID | 0 | 1 | G | BID | |||||||
| 126252741 | 12625274 | 5 | SS | PLAQUENIL | HYDROXYCHLOROQUINE SULFATE | 1 | Unknown | 400 MG, QD | 0 | 400 | MG | QD | |||||||
| 126252741 | 12625274 | 6 | C | PREDNISONE. | PREDNISONE | 1 | 5 MG, QD | 0 | 5 | MG | QD |
Indications of drugs used
| Event ID | CASEID | INDI DRUG SEQ | INDI PT |
|---|---|---|---|
| 126252741 | 12625274 | 1 | Rheumatoid arthritis |
| 126252741 | 12625274 | 2 | Product used for unknown indication |
| 126252741 | 12625274 | 3 | Product used for unknown indication |
| 126252741 | 12625274 | 4 | Rheumatoid arthritis |
| 126252741 | 12625274 | 5 | Product used for unknown indication |
Outcome of event
| Event ID | CASEID | OUTC COD |
|---|---|---|
| 126252741 | 12625274 | OT |
Reactions reported
| Event ID | CASEID | DRUG REC ACT | PT |
|---|---|---|---|
| 126252741 | 12625274 | Anxiety | |
| 126252741 | 12625274 | Drug ineffective | |
| 126252741 | 12625274 | Drug intolerance | |
| 126252741 | 12625274 | Palpitations | |
| 126252741 | 12625274 | Rash | |
| 126252741 | 12625274 | Rheumatoid arthritis | |
| 126252741 | 12625274 | Therapeutic response decreased |
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 |
|---|---|---|---|---|---|---|
| 126252741 | 12625274 | 1 | 201303 | 201506 | 0 | |
| 126252741 | 12625274 | 3 | 2002 | 0 |