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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 99237252 | 9923725 | 2 | F | 2003 | 20160719 | 20140225 | 20160729 | PER | US-AMGEN-USASP2014001055 | AMGEN | 44.00 | YR | A | F | Y | 0.00000 | 20160729 | 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 99237252 | 9923725 | 1 | PS | ENBREL | ETANERCEPT | 1 | Unknown | UNK | Y | 103795 | SOLUTION FOR INJECTION IN PRE-FILLED SYRINGE | ||||||||
| 99237252 | 9923725 | 2 | SS | ENBREL | ETANERCEPT | 1 | Unknown | UNK | Y | 103795 | SOLUTION FOR INJECTION IN PRE-FILLED SYRINGE | ||||||||
| 99237252 | 9923725 | 3 | SS | ENBREL | ETANERCEPT | 1 | Unknown | 50 MG, QWK | Y | 103795 | 50 | MG | SOLUTION FOR INJECTION IN PRE-FILLED SYRINGE | /wk | |||||
| 99237252 | 9923725 | 4 | SS | ORENCIA | ABATACEPT | 1 | Unknown | UNK | 0 | ||||||||||
| 99237252 | 9923725 | 5 | C | PREDNISONE. | PREDNISONE | 1 | UNK | 0 | |||||||||||
| 99237252 | 9923725 | 6 | C | PLAQUENIL | HYDROXYCHLOROQUINE SULFATE | 1 | UNK | 0 | |||||||||||
| 99237252 | 9923725 | 7 | C | REMICADE | INFLIXIMAB | 1 | UNK | 0 |
Indications of drugs used
| Event ID | CASEID | INDI DRUG SEQ | INDI PT |
|---|---|---|---|
| 99237252 | 9923725 | 1 | Rheumatoid arthritis |
| 99237252 | 9923725 | 4 | Product used for unknown indication |
Outcome of event
| no results found |
Reactions reported
| Event ID | CASEID | DRUG REC ACT | PT |
|---|---|---|---|
| 99237252 | 9923725 | Condition aggravated | |
| 99237252 | 9923725 | Drug effect decreased | |
| 99237252 | 9923725 | Injection site bruising | |
| 99237252 | 9923725 | Injection site mass | |
| 99237252 | 9923725 | Injection site pain | |
| 99237252 | 9923725 | Respiratory disorder |
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 |
|---|---|---|---|---|---|---|
| 99237252 | 9923725 | 1 | 2003 | 0 | ||
| 99237252 | 9923725 | 2 | 2005 | 0 | ||
| 99237252 | 9923725 | 3 | 20131115 | 0 |