The Safety Rates Drug Report

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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
125843011 12584301 1 I 20151102 20160722 20160722 EXP CA-PFIZER INC-2015375987 PFIZER 44.00 YR 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
125843011 12584301 1 SS ENBREL ETANERCEPT 1 UNK 0
125843011 12584301 2 PS METHOTREXATE SODIUM. METHOTREXATE SODIUM 1 20 DF, WEEKLY 11719 20 DF /wk
125843011 12584301 3 SS LEFLUNOMIDE. LEFLUNOMIDE 1 20 DF, 1X/DAY U 0 20 DF TABLET QD
125843011 12584301 4 SS PLAQUENIL HYDROXYCHLOROQUINE SULFATE 1 400 MG, 1X/DAY 0 400 MG TABLET QD
125843011 12584301 5 SS HUMIRA ADALIMUMAB 1 0
125843011 12584301 6 SS ORENCIA ABATACEPT 1 UNK 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
125843011 12584301 1 Rheumatoid arthritis
125843011 12584301 2 Rheumatoid arthritis
125843011 12584301 3 Rheumatoid arthritis
125843011 12584301 4 Rheumatoid arthritis
125843011 12584301 5 Rheumatoid arthritis
125843011 12584301 6 Rheumatoid arthritis

Outcome of event

Event ID CASEID OUTC COD
125843011 12584301 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
125843011 12584301 Arthralgia
125843011 12584301 Drug ineffective
125843011 12584301 Drug intolerance
125843011 12584301 Gastric ulcer
125843011 12584301 Treatment failure

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
125843011 12584301 6 201508 0