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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 125802362 | 12580236 | 2 | F | 2016 | 20160715 | 20160721 | 20160725 | EXP | CA-AMGEN-CANSP2016093623 | AMGEN | 60.00 | YR | A | F | Y | 0.00000 | 20160725 | 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 125802362 | 12580236 | 1 | PS | ENBREL | ETANERCEPT | 1 | Unknown | UNK | U | 103795 | UNKNOWN FORMULATION | ||||||||
| 125802362 | 12580236 | 2 | SS | ENBREL | ETANERCEPT | 1 | Unknown | UNK | U | 103795 | UNKNOWN FORMULATION | ||||||||
| 125802362 | 12580236 | 3 | SS | METHOTREXATE. | METHOTREXATE | 1 | Unknown | 20 MG, UNK | 0 | 20 | MG | ||||||||
| 125802362 | 12580236 | 4 | SS | HYDROXYCHLOROQUINE | HYDROXYCHLOROQUINE | 1 | Unknown | 400 MG, UNK | 0 | 400 | MG | ||||||||
| 125802362 | 12580236 | 5 | SS | SULFASALAZINE. | SULFASALAZINE | 1 | Oral | 1 G, BID | 0 | 1 | G | BID | |||||||
| 125802362 | 12580236 | 6 | SS | HUMIRA | ADALIMUMAB | 1 | Unknown | UNK | 0 |
Indications of drugs used
| Event ID | CASEID | INDI DRUG SEQ | INDI PT |
|---|---|---|---|
| 125802362 | 12580236 | 1 | Rheumatoid arthritis |
| 125802362 | 12580236 | 3 | Rheumatoid arthritis |
| 125802362 | 12580236 | 4 | Rheumatoid arthritis |
| 125802362 | 12580236 | 5 | Rheumatoid arthritis |
| 125802362 | 12580236 | 6 | Rheumatoid arthritis |
Outcome of event
| Event ID | CASEID | OUTC COD |
|---|---|---|
| 125802362 | 12580236 | OT |
Reactions reported
| Event ID | CASEID | DRUG REC ACT | PT |
|---|---|---|---|
| 125802362 | 12580236 | Abdominal pain upper | |
| 125802362 | 12580236 | Drug hypersensitivity | |
| 125802362 | 12580236 | Drug intolerance | |
| 125802362 | 12580236 | Faeces soft | |
| 125802362 | 12580236 | 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 |
|---|---|---|---|---|---|---|
| 125802362 | 12580236 | 1 | 2013 | 0 | ||
| 125802362 | 12580236 | 2 | 201602 | 2016 | 0 | |
| 125802362 | 12580236 | 3 | 2013 | 2014 | 0 | |
| 125802362 | 12580236 | 4 | 201307 | 201311 | 0 | |
| 125802362 | 12580236 | 5 | 201407 | 201411 | 0 | |
| 125802362 | 12580236 | 6 | 201601 | 0 |