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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 126008661 | 12600866 | 1 | I | 20160626 | 20160718 | 20160727 | 20160727 | EXP | FR-AMGEN-FRASP2016096263 | AMGEN | 48.00 | YR | A | F | Y | 0.00000 | 20160727 | OT | FR | FR |
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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 126008661 | 12600866 | 1 | PS | ENBREL | ETANERCEPT | 1 | Subcutaneous | 50 MG, WEEKLY | 50 | MG | Y | 103795 | 50 | MG | POWDER AND SOLVENT FOR SOLUTION FOR INJECTION | /wk | |||
| 126008661 | 12600866 | 2 | SS | CORTANCYL | PREDNISONE | 1 | Oral | 15 MG, 1X/DAY | 90 | MG | 0 | 15 | MG | QD | |||||
| 126008661 | 12600866 | 3 | C | BIPROFENID | KETOPROFEN | 1 | UNK | 0 | |||||||||||
| 126008661 | 12600866 | 4 | C | ALPRAZOLAM. | ALPRAZOLAM | 1 | UNK | 0 | |||||||||||
| 126008661 | 12600866 | 5 | C | MACROGOL STEARATE | POLYETHYLENE GLYCOLS | 1 | UNK | 0 | |||||||||||
| 126008661 | 12600866 | 6 | C | DAFALGAN | ACETAMINOPHEN | 1 | UNK | 0 | |||||||||||
| 126008661 | 12600866 | 7 | C | OXYNORM | OXYCODONE HYDROCHLORIDE | 1 | UNK | 0 | |||||||||||
| 126008661 | 12600866 | 8 | C | OXYCONTIN | OXYCODONE HYDROCHLORIDE | 1 | UNK | 0 | |||||||||||
| 126008661 | 12600866 | 9 | C | OXYCONTIN | OXYCODONE HYDROCHLORIDE | 1 | 0 |
Indications of drugs used
| Event ID | CASEID | INDI DRUG SEQ | INDI PT |
|---|---|---|---|
| 126008661 | 12600866 | 1 | Rheumatoid arthritis |
| 126008661 | 12600866 | 2 | Rheumatoid arthritis |
| 126008661 | 12600866 | 8 | Pain |
| 126008661 | 12600866 | 9 | Rheumatoid arthritis |
Outcome of event
| Event ID | CASEID | OUTC COD |
|---|---|---|
| 126008661 | 12600866 | HO |
| 126008661 | 12600866 | OT |
Reactions reported
| Event ID | CASEID | DRUG REC ACT | PT |
|---|---|---|---|
| 126008661 | 12600866 | Arthritis bacterial | |
| 126008661 | 12600866 | Back pain | |
| 126008661 | 12600866 | Drug effect incomplete | |
| 126008661 | 12600866 | Endocarditis staphylococcal | |
| 126008661 | 12600866 | 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 |
|---|---|---|---|---|---|---|
| 126008661 | 12600866 | 1 | 201511 | 20160701 | 0 | |
| 126008661 | 12600866 | 2 | 20160701 | 20160706 | 0 | |
| 126008661 | 12600866 | 3 | 20160701 | 0 |