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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 69805193 | 6980519 | 3 | F | 2008 | 20160801 | 20090429 | 20160810 | EXP | US-AMGEN-QUU343746 | AMGEN | 73.00 | YR | E | F | Y | 0.00000 | 20160810 | MD | US | US |
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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 69805193 | 6980519 | 1 | PS | ENBREL | ETANERCEPT | 1 | Subcutaneous | 50 MG, QWK | Y | 1054341 | 103795 | 50 | MG | SOLUTION FOR INJECTION IN PRE-FILLED SYRINGE | /wk | ||||
| 69805193 | 6980519 | 2 | SS | ENBREL | ETANERCEPT | 1 | Unknown | UNK | Y | 1051348 | 103795 | SOLUTION FOR INJECTION IN PRE-FILLED SYRINGE | |||||||
| 69805193 | 6980519 | 3 | SS | ENBREL | ETANERCEPT | 1 | Unknown | UNK | Y | 1063527 | 103795 | SOLUTION FOR INJECTION IN PRE-FILLED SYRINGE | |||||||
| 69805193 | 6980519 | 4 | C | METHOTREXATE. | METHOTREXATE | 1 | Oral | 12.5 MG, QWK | 0 | 12.5 | MG | /wk | |||||||
| 69805193 | 6980519 | 5 | C | CALCIUM | CALCIUM | 1 | UNK | 0 | |||||||||||
| 69805193 | 6980519 | 6 | C | VITAMIN D3 | CHOLECALCIFEROL | 1 | UNK | 0 | |||||||||||
| 69805193 | 6980519 | 7 | C | TYLENOL | ACETAMINOPHEN | 1 | UNK | 0 | |||||||||||
| 69805193 | 6980519 | 8 | C | HYDROXYCHLOROQUINE SULFATE. | HYDROXYCHLOROQUINE SULFATE | 1 | Oral | 200 MG, QD | 0 | 200 | MG | QD |
Indications of drugs used
| Event ID | CASEID | INDI DRUG SEQ | INDI PT |
|---|---|---|---|
| 69805193 | 6980519 | 1 | Rheumatoid arthritis |
| 69805193 | 6980519 | 2 | Arthritis |
| 69805193 | 6980519 | 3 | Psoriatic arthropathy |
| 69805193 | 6980519 | 4 | Rheumatoid arthritis |
Outcome of event
| Event ID | CASEID | OUTC COD |
|---|---|---|
| 69805193 | 6980519 | HO |
| 69805193 | 6980519 | OT |
Reactions reported
| Event ID | CASEID | DRUG REC ACT | PT |
|---|---|---|---|
| 69805193 | 6980519 | Arthralgia | |
| 69805193 | 6980519 | Atrial fibrillation | |
| 69805193 | 6980519 | Barrett's oesophagus | |
| 69805193 | 6980519 | Breast neoplasm | |
| 69805193 | 6980519 | Foot deformity | |
| 69805193 | 6980519 | Impaired healing | |
| 69805193 | 6980519 | Infection | |
| 69805193 | 6980519 | Injection site pain | |
| 69805193 | 6980519 | Macular degeneration | |
| 69805193 | 6980519 | Ovarian cancer | |
| 69805193 | 6980519 | Pain | |
| 69805193 | 6980519 | Rheumatoid arthritis | |
| 69805193 | 6980519 | Skin ulcer | |
| 69805193 | 6980519 | Uterine cancer | |
| 69805193 | 6980519 | Wisdom teeth removal |
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 |
|---|---|---|---|---|---|---|
| 69805193 | 6980519 | 1 | 200411 | 0 |