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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
125833971 | 12583397 | 1 | I | 201309 | 20151023 | 20160722 | 20160722 | EXP | CA-PFIZER INC-2015363640 | PFIZER | 0.00 | F | Y | 0.00000 | 20160722 | 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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
125833971 | 12583397 | 1 | SS | ENBREL | ETANERCEPT | 1 | 50 MG, UNK | 0 | 50 | MG | |||||||||
125833971 | 12583397 | 2 | PS | METHOTREXATE SODIUM. | METHOTREXATE SODIUM | 1 | Subcutaneous | 20 MG, WEEKLY | U | 11719 | 20 | MG | /wk | ||||||
125833971 | 12583397 | 3 | SS | SULFASALAZINE. | SULFASALAZINE | 1 | 1000 MG, 2X/DAY | 7073 | 1000 | MG | BID | ||||||||
125833971 | 12583397 | 4 | SS | HUMIRA | ADALIMUMAB | 1 | 20 MG, DAILY | 0 | 20 | MG | |||||||||
125833971 | 12583397 | 5 | SS | PREDNISONE. | PREDNISONE | 1 | Oral | 5 MG, DAILY | 0 | 5 | MG | ||||||||
125833971 | 12583397 | 6 | SS | ARAVA | LEFLUNOMIDE | 1 | 20 MG, DAILY | 0 | 20 | MG | TABLET | ||||||||
125833971 | 12583397 | 7 | SS | PLAQUENIL | HYDROXYCHLOROQUINE SULFATE | 1 | 200 MG, 2X/DAY | U | 0 | 200 | MG | TABLET | BID | ||||||
125833971 | 12583397 | 8 | SS | ORENCIA | ABATACEPT | 1 | UNK | 0 | |||||||||||
125833971 | 12583397 | 9 | SS | ACTEMRA | TOCILIZUMAB | 1 | UNK | U | 0 |
Indications of drugs used
Event ID | CASEID | INDI DRUG SEQ | INDI PT |
---|---|---|---|
125833971 | 12583397 | 1 | Rheumatoid arthritis |
125833971 | 12583397 | 2 | Rheumatoid arthritis |
125833971 | 12583397 | 3 | Rheumatoid arthritis |
125833971 | 12583397 | 7 | Rheumatoid arthritis |
Outcome of event
Event ID | CASEID | OUTC COD |
---|---|---|
125833971 | 12583397 | OT |
Reactions reported
Event ID | CASEID | DRUG REC ACT | PT |
---|---|---|---|
125833971 | 12583397 | Activities of daily living impaired | |
125833971 | 12583397 | Arthralgia | |
125833971 | 12583397 | Condition aggravated | |
125833971 | 12583397 | Drug ineffective | |
125833971 | 12583397 | Fatigue | |
125833971 | 12583397 | Joint swelling | |
125833971 | 12583397 | Pain | |
125833971 | 12583397 | Peripheral swelling | |
125833971 | 12583397 | Rheumatoid arthritis |
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 |
---|---|---|---|---|---|---|
125833971 | 12583397 | 1 | 20130618 | 201309 | 0 | |
125833971 | 12583397 | 2 | 20130130 | 0 | ||
125833971 | 12583397 | 3 | 20121213 | 0 | ||
125833971 | 12583397 | 4 | 20130313 | 201309 | 0 | |
125833971 | 12583397 | 5 | 20130313 | 0 | ||
125833971 | 12583397 | 6 | 20130313 | 0 | ||
125833971 | 12583397 | 7 | 20121213 | 0 | ||
125833971 | 12583397 | 8 | 201309 | 201406 | 0 | |
125833971 | 12583397 | 9 | 201406 | 0 |