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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 87782244 | 8778224 | 4 | F | 2012 | 20160915 | 20120911 | 20160922 | EXP | BR-AMGEN-BRASP2012056192 | AMGEN | 54.00 | YR | A | F | Y | 57.00000 | KG | 20160922 | OT | 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 87782244 | 8778224 | 1 | PS | ENBREL | ETANERCEPT | 1 | Subcutaneous | 50 MG, ONCE WEEKLY | F95872 | 103795 | 50 | MG | SOLUTION FOR INJECTION IN PRE-FILLED SYRINGE | /wk | |||||
| 87782244 | 8778224 | 2 | SS | METHOTREXATE SODIUM. | METHOTREXATE SODIUM | 1 | Unknown | UNK, WEEKLY | 0 | /wk | |||||||||
| 87782244 | 8778224 | 3 | C | ARAVA | LEFLUNOMIDE | 1 | 20 MG, 1X/DAY | 0 | |||||||||||
| 87782244 | 8778224 | 4 | C | NIMESULIDE | NIMESULIDE | 1 | 20 MG, UNK | 0 | 20 | MG | |||||||||
| 87782244 | 8778224 | 5 | C | CORTIZONE 10 | HYDROCORTISONE | 1 | UNK | 0 |
Indications of drugs used
| Event ID | CASEID | INDI DRUG SEQ | INDI PT |
|---|---|---|---|
| 87782244 | 8778224 | 1 | Rheumatoid arthritis |
| 87782244 | 8778224 | 2 | Rheumatoid arthritis |
| 87782244 | 8778224 | 3 | Rheumatoid arthritis |
| 87782244 | 8778224 | 4 | Rheumatoid arthritis |
Outcome of event
| Event ID | CASEID | OUTC COD |
|---|---|---|
| 87782244 | 8778224 | OT |
Reactions reported
| Event ID | CASEID | DRUG REC ACT | PT |
|---|---|---|---|
| 87782244 | 8778224 | Haematoma | |
| 87782244 | 8778224 | Hyperaemia | |
| 87782244 | 8778224 | Injection site erythema | |
| 87782244 | 8778224 | Injection site mass | |
| 87782244 | 8778224 | Injection site pain | |
| 87782244 | 8778224 | Injection site pruritus | |
| 87782244 | 8778224 | Injection site ulcer | |
| 87782244 | 8778224 | Lung disorder | |
| 87782244 | 8778224 | Nausea | |
| 87782244 | 8778224 | Pruritus |
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 |
|---|---|---|---|---|---|---|
| 87782244 | 8778224 | 1 | 201208 | 201301 | 0 | |
| 87782244 | 8778224 | 2 | 20120904 | 0 |