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
125810671 12581067 1 I 20160714 20160721 20160721 EXP CA-PFIZER INC-2016352283 PFIZER 74.00 YR F Y 0.00000 20160721 MD 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
125810671 12581067 1 SS ENBREL ETANERCEPT 1 Subcutaneous UNK U 0
125810671 12581067 2 PS METHOTREXATE SODIUM. METHOTREXATE SODIUM 1 Unknown UNK U 11719
125810671 12581067 3 SS REMICADE INFLIXIMAB 1 Intravenous (not otherwise specified) UNK U 0
125810671 12581067 4 SS ANAKINRA ANAKINRA 1 Unknown UNK U 0
125810671 12581067 5 SS HYDROXYCHLOROQUINE HYDROXYCHLOROQUINE 1 Unknown UNK U 0 TABLET
125810671 12581067 6 SS IMURAN AZATHIOPRINE 1 Unknown UNK U 0
125810671 12581067 7 SS LEFLUNOMIDE. LEFLUNOMIDE 1 Unknown UNK U 0 TABLET
125810671 12581067 8 SS RITUXAN RITUXIMAB 1 Intravenous (not otherwise specified) UNK U 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
125810671 12581067 1 Rheumatoid arthritis

Outcome of event

Event ID CASEID OUTC COD
125810671 12581067 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
125810671 12581067 Rheumatoid arthritis
125810671 12581067 Treatment failure

Reporting Sources (this data is often not reported and may therefore be missing here)

no results found

Therapies reported

no results found