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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 120721703 | 12072170 | 3 | F | 201507 | 20160825 | 20160212 | 20160830 | EXP | CA-AMGEN-CANSP2016016415 | AMGEN | 72.00 | YR | E | 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 120721703 | 12072170 | 1 | PS | ENBREL | ETANERCEPT | 1 | Unknown | UNK | U | 103795 | UNKNOWN FORMULATION | ||||||||
| 120721703 | 12072170 | 2 | SS | HUMIRA | ADALIMUMAB | 1 | Unknown | UNK | 0 | ||||||||||
| 120721703 | 12072170 | 3 | SS | METHOTREXATE SODIUM. | METHOTREXATE SODIUM | 1 | Unknown | UNK | 0 | ||||||||||
| 120721703 | 12072170 | 4 | C | TRAMADOL. | TRAMADOL | 1 | UNK | 0 |
Indications of drugs used
| Event ID | CASEID | INDI DRUG SEQ | INDI PT |
|---|---|---|---|
| 120721703 | 12072170 | 1 | Rheumatoid arthritis |
| 120721703 | 12072170 | 2 | Product used for unknown indication |
| 120721703 | 12072170 | 3 | Rheumatoid arthritis |
Outcome of event
| Event ID | CASEID | OUTC COD |
|---|---|---|
| 120721703 | 12072170 | OT |
Reactions reported
| Event ID | CASEID | DRUG REC ACT | PT |
|---|---|---|---|
| 120721703 | 12072170 | Alopecia | |
| 120721703 | 12072170 | Diabetes mellitus | |
| 120721703 | 12072170 | Drug effect decreased | |
| 120721703 | 12072170 | Drug ineffective | |
| 120721703 | 12072170 | Herpes zoster | |
| 120721703 | 12072170 | Hypertension | |
| 120721703 | 12072170 | Multiple sclerosis | |
| 120721703 | 12072170 | Oedema peripheral | |
| 120721703 | 12072170 | Renal impairment | |
| 120721703 | 12072170 | Skin discolouration | |
| 120721703 | 12072170 | Thyroid disorder | |
| 120721703 | 12072170 | Weight increased |
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 |
|---|---|---|---|---|---|---|
| 120721703 | 12072170 | 1 | 2000 | 201507 | 0 |