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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 116888843 | 11688884 | 3 | F | 20160714 | 20151102 | 20160719 | EXP | CA-AMGEN-CANSP2015114325 | AMGEN | 71.00 | YR | E | F | Y | 0.00000 | 20160719 | OT | CA | CA |
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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 116888843 | 11688884 | 1 | PS | ENBREL | ETANERCEPT | 1 | Unknown | UNK | U | 103795 | UNKNOWN FORMULATION | ||||||||
| 116888843 | 11688884 | 2 | SS | PLAQUENIL | HYDROXYCHLOROQUINE SULFATE | 1 | Unknown | UNK | 0 | TABLET | |||||||||
| 116888843 | 11688884 | 3 | SS | GOLD | GOLD | 1 | Unknown | UNK | 0 | INJECTION | |||||||||
| 116888843 | 11688884 | 4 | SS | METHOTREXATE SODIUM. | METHOTREXATE SODIUM | 1 | Unknown | UNK | 0 | ||||||||||
| 116888843 | 11688884 | 5 | SS | SIMPONI | GOLIMUMAB | 1 | Unknown | UNK | 0 | ||||||||||
| 116888843 | 11688884 | 6 | SS | ACTEMRA | TOCILIZUMAB | 1 | Unknown | UNK | 0 | ||||||||||
| 116888843 | 11688884 | 7 | C | CELEBREX | CELECOXIB | 1 | UNK | 0 | |||||||||||
| 116888843 | 11688884 | 8 | C | CIMZIA | CERTOLIZUMAB PEGOL | 1 | UNK | 0 | |||||||||||
| 116888843 | 11688884 | 9 | C | FOLIC ACID. | FOLIC ACID | 1 | UNK | 0 |
Indications of drugs used
| Event ID | CASEID | INDI DRUG SEQ | INDI PT |
|---|---|---|---|
| 116888843 | 11688884 | 1 | Rheumatoid arthritis |
| 116888843 | 11688884 | 2 | Rheumatoid arthritis |
| 116888843 | 11688884 | 3 | Rheumatoid arthritis |
| 116888843 | 11688884 | 4 | Rheumatoid arthritis |
| 116888843 | 11688884 | 5 | Rheumatoid arthritis |
| 116888843 | 11688884 | 6 | Rheumatoid arthritis |
Outcome of event
| Event ID | CASEID | OUTC COD |
|---|---|---|
| 116888843 | 11688884 | OT |
Reactions reported
| Event ID | CASEID | DRUG REC ACT | PT |
|---|---|---|---|
| 116888843 | 11688884 | Burning sensation | |
| 116888843 | 11688884 | Discomfort | |
| 116888843 | 11688884 | Drug ineffective | |
| 116888843 | 11688884 | Hyperaesthesia | |
| 116888843 | 11688884 | Memory impairment | |
| 116888843 | 11688884 | Pain | |
| 116888843 | 11688884 | Rheumatoid arthritis | |
| 116888843 | 11688884 | Therapeutic response decreased |
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 |
|---|---|---|---|---|---|---|
| 116888843 | 11688884 | 8 | 20151019 | 0 |