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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 118836764 | 11883676 | 4 | F | 2015 | 20160119 | 20160101 | 20160823 | PER | US-AMGEN-USASP2015138494 | AMGEN | 61.00 | YR | A | M | Y | 0.00000 | 20160823 | 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 118836764 | 11883676 | 1 | PS | ENBREL | ETANERCEPT | 1 | Unknown | UNK | U | 1059239 | 103795 | SOLUTION FOR INJECTION IN PRE-FILLED SYRINGE |
Indications of drugs used
| Event ID | CASEID | INDI DRUG SEQ | INDI PT |
|---|---|---|---|
| 118836764 | 11883676 | 1 | Ankylosing spondylitis |
Outcome of event
| no results found |
Reactions reported
| Event ID | CASEID | DRUG REC ACT | PT |
|---|---|---|---|
| 118836764 | 11883676 | Injection site haemorrhage | |
| 118836764 | 11883676 | Injection site induration | |
| 118836764 | 11883676 | Injection site pruritus | |
| 118836764 | 11883676 | Injection site reaction | |
| 118836764 | 11883676 | Somnolence | |
| 118836764 | 11883676 | Underdose | |
| 118836764 | 11883676 | Wrong technique in product usage process |
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 |
|---|---|---|---|---|---|---|
| 118836764 | 11883676 | 1 | 20151110 | 0 |