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
125810391 12581039 1 I 20160427 20160721 20160721 EXP CA-PFIZER INC-2016246968 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
125810391 12581039 1 SS ENBREL ETANERCEPT 1 Subcutaneous UNK U 0
125810391 12581039 2 PS METHOTREXATE SODIUM. METHOTREXATE SODIUM 1 Unknown UNK U 11719
125810391 12581039 3 SS ANAKINRA ANAKINRA 1 Unknown UNK U 0
125810391 12581039 4 SS HYDROXYCHLOROQUINE HYDROXYCHLOROQUINE 1 Unknown UNK U 0 TABLET
125810391 12581039 5 SS IMURAN AZATHIOPRINE 1 Unknown UNK U 0
125810391 12581039 6 SS LEFLUNOMIDE. LEFLUNOMIDE 1 Unknown UNK U 0 TABLET
125810391 12581039 7 SS REMICADE INFLIXIMAB 1 Intravenous (not otherwise specified) UNK U 0
125810391 12581039 8 SS RITUXAN RITUXIMAB 1 Unknown UNK U 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
125810391 12581039 1 Rheumatoid arthritis

Outcome of event

Event ID CASEID OUTC COD
125810391 12581039 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
125810391 12581039 Rheumatoid arthritis
125810391 12581039 Treatment failure

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

no results found

Therapies reported

no results found