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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 118498784 | 11849878 | 4 | F | 2015 | 20160725 | 20151218 | 20160728 | EXP | CA-AMGEN-CANSP2015134910 | AMGEN | 0.00 | F | Y | 0.00000 | 20160728 | 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 118498784 | 11849878 | 1 | PS | ENBREL | ETANERCEPT | 1 | Unknown | UNK | U | 103795 | UNKNOWN FORMULATION | ||||||||
| 118498784 | 11849878 | 2 | SS | GOLD | GOLD | 1 | Unknown | UNK | 0 | ||||||||||
| 118498784 | 11849878 | 3 | SS | MINOCYCLINE | MINOCYCLINEMINOCYCLINE HYDROCHLORIDE | 1 | Unknown | UNK | 0 | ||||||||||
| 118498784 | 11849878 | 4 | SS | PLAQUENIL | HYDROXYCHLOROQUINE SULFATE | 1 | Unknown | UNK | 0 | ||||||||||
| 118498784 | 11849878 | 5 | SS | HUMIRA | ADALIMUMAB | 1 | Unknown | UNK | 0 | ||||||||||
| 118498784 | 11849878 | 6 | SS | ORENCIA | ABATACEPT | 1 | Intravenous (not otherwise specified) | UNK | 0 | ||||||||||
| 118498784 | 11849878 | 7 | SS | PREDNISONE. | PREDNISONE | 1 | Unknown | 3 MG, UNK | 0 | 3 | MG | ||||||||
| 118498784 | 11849878 | 8 | SS | METHOTREXATE SODIUM. | METHOTREXATE SODIUM | 1 | Unknown | 20 MG, QWK | 0 | 20 | MG | /wk |
Indications of drugs used
| Event ID | CASEID | INDI DRUG SEQ | INDI PT |
|---|---|---|---|
| 118498784 | 11849878 | 1 | Rheumatoid arthritis |
| 118498784 | 11849878 | 2 | Product used for unknown indication |
| 118498784 | 11849878 | 3 | Product used for unknown indication |
| 118498784 | 11849878 | 4 | Rheumatoid arthritis |
| 118498784 | 11849878 | 5 | Rheumatoid arthritis |
| 118498784 | 11849878 | 6 | Rheumatoid arthritis |
| 118498784 | 11849878 | 7 | Rheumatoid arthritis |
| 118498784 | 11849878 | 8 | Product used for unknown indication |
Outcome of event
| Event ID | CASEID | OUTC COD |
|---|---|---|
| 118498784 | 11849878 | OT |
Reactions reported
| Event ID | CASEID | DRUG REC ACT | PT |
|---|---|---|---|
| 118498784 | 11849878 | Arthralgia | |
| 118498784 | 11849878 | Condition aggravated | |
| 118498784 | 11849878 | Disability | |
| 118498784 | 11849878 | Drug effect decreased | |
| 118498784 | 11849878 | Drug ineffective | |
| 118498784 | 11849878 | Musculoskeletal stiffness | |
| 118498784 | 11849878 | Pain |
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 |
|---|---|---|---|---|---|---|
| 118498784 | 11849878 | 6 | 20151203 | 0 |