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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 106762007 | 10676200 | 7 | F | 2014 | 20160628 | 20141226 | 20160708 | EXP | AR-AMGEN-ARGSP2014100304 | AMGEN | 69.00 | YR | E | F | Y | 0.00000 | 20160708 | CN | AR | AR |
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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 106762007 | 10676200 | 1 | PS | ENBREL | ETANERCEPT | 1 | Unknown | 50 MG, WEEKLY | Y | 103795 | 50 | MG | SOLUTION FOR INJECTION IN PRE-FILLED SYRINGE | /wk |
Indications of drugs used
| Event ID | CASEID | INDI DRUG SEQ | INDI PT |
|---|---|---|---|
| 106762007 | 10676200 | 1 | Rheumatoid arthritis |
Outcome of event
| Event ID | CASEID | OUTC COD |
|---|---|---|
| 106762007 | 10676200 | OT |
| 106762007 | 10676200 | HO |
Reactions reported
| Event ID | CASEID | DRUG REC ACT | PT |
|---|---|---|---|
| 106762007 | 10676200 | Arthritis | |
| 106762007 | 10676200 | Balance disorder | |
| 106762007 | 10676200 | Blood pressure decreased | |
| 106762007 | 10676200 | Blood pressure fluctuation | |
| 106762007 | 10676200 | Blood sodium decreased | |
| 106762007 | 10676200 | Blood test normal | |
| 106762007 | 10676200 | Burning sensation | |
| 106762007 | 10676200 | Cervix disorder | |
| 106762007 | 10676200 | Condition aggravated | |
| 106762007 | 10676200 | Conjunctivitis viral | |
| 106762007 | 10676200 | Decreased immune responsiveness | |
| 106762007 | 10676200 | Diarrhoea | |
| 106762007 | 10676200 | Eye disorder | |
| 106762007 | 10676200 | Gait disturbance | |
| 106762007 | 10676200 | Headache | |
| 106762007 | 10676200 | Hypertension | |
| 106762007 | 10676200 | Insomnia | |
| 106762007 | 10676200 | Irritable bowel syndrome | |
| 106762007 | 10676200 | Ligament rupture | |
| 106762007 | 10676200 | Malaise | |
| 106762007 | 10676200 | Memory impairment | |
| 106762007 | 10676200 | Meniscus injury | |
| 106762007 | 10676200 | Mobility decreased | |
| 106762007 | 10676200 | Pain | |
| 106762007 | 10676200 | Pulmonary pain | |
| 106762007 | 10676200 | Spinal disorder | |
| 106762007 | 10676200 | Varicella zoster virus infection |
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 |
|---|---|---|---|---|---|---|
| 106762007 | 10676200 | 1 | 20080114 | 0 |