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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 125806481 | 12580648 | 1 | I | 2007 | 20151106 | 20160721 | 20160721 | EXP | CA-PFIZER INC-2015383958 | PFIZER | 49.00 | YR | F | Y | 0.00000 | 20160721 | CN | 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 125806481 | 12580648 | 1 | SS | ENBREL | ETANERCEPT | 1 | UNK | 0 | |||||||||||
| 125806481 | 12580648 | 2 | PS | METHOTREXATE SODIUM. | METHOTREXATE SODIUM | 1 | 25 MG, UNK | 11719 | 25 | MG | |||||||||
| 125806481 | 12580648 | 3 | SS | SULFASALAZINE. | SULFASALAZINE | 1 | 1500 MG, UNK | 7073 | 1500 | MG | |||||||||
| 125806481 | 12580648 | 4 | SS | HYDROXYCHLOROQUINE | HYDROXYCHLOROQUINE | 1 | 200 MG, DAILY | 0 | 200 | MG | |||||||||
| 125806481 | 12580648 | 5 | SS | ARAVA | LEFLUNOMIDE | 1 | 10 MG, DAILY | 0 | 10 | MG | TABLET | ||||||||
| 125806481 | 12580648 | 6 | SS | REMICADE | INFLIXIMAB | 1 | UNK | 0 | |||||||||||
| 125806481 | 12580648 | 7 | SS | ORENCIA | ABATACEPT | 1 | UNK | 0 | |||||||||||
| 125806481 | 12580648 | 8 | SS | ACTEMRA | TOCILIZUMAB | 1 | UNK | 0 | |||||||||||
| 125806481 | 12580648 | 9 | C | KINERET | ANAKINRA | 1 | UNK | 0 |
Indications of drugs used
| Event ID | CASEID | INDI DRUG SEQ | INDI PT |
|---|---|---|---|
| 125806481 | 12580648 | 1 | Rheumatoid arthritis |
| 125806481 | 12580648 | 2 | Rheumatoid arthritis |
| 125806481 | 12580648 | 3 | Rheumatoid arthritis |
| 125806481 | 12580648 | 4 | Rheumatoid arthritis |
| 125806481 | 12580648 | 5 | Rheumatoid arthritis |
| 125806481 | 12580648 | 6 | Rheumatoid arthritis |
| 125806481 | 12580648 | 7 | Rheumatoid arthritis |
| 125806481 | 12580648 | 8 | Rheumatoid arthritis |
Outcome of event
| Event ID | CASEID | OUTC COD |
|---|---|---|
| 125806481 | 12580648 | OT |
Reactions reported
| Event ID | CASEID | DRUG REC ACT | PT |
|---|---|---|---|
| 125806481 | 12580648 | Drug hypersensitivity | |
| 125806481 | 12580648 | Drug ineffective | |
| 125806481 | 12580648 | Drug intolerance | |
| 125806481 | 12580648 | Hepatitis | |
| 125806481 | 12580648 | Vomiting |
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 |
|---|---|---|---|---|---|---|
| 125806481 | 12580648 | 2 | 2007 | 2008 | 0 | |
| 125806481 | 12580648 | 5 | 2008 | 0 | ||
| 125806481 | 12580648 | 8 | 20151030 | 0 |