The Safety Rates Drug Report

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Drug     Injury     Quarter    

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
124966334 12496633 4 F 2013 20160810 20160624 20160818 EXP CA-PFIZER INC-2016311785 PFIZER 60.00 YR F Y 0.00000 20160818 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
124966334 12496633 1 PS METHOTREXATE SODIUM. METHOTREXATE SODIUM 1 UNK Y 11719
124966334 12496633 2 SS HYDROXYCHLOROQUINE HYDROXYCHLOROQUINE 1 UNK Y 0
124966334 12496633 3 C LEFLUNOMIDE. LEFLUNOMIDE 1 UNK 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
124966334 12496633 1 Rheumatoid arthritis

Outcome of event

Event ID CASEID OUTC COD
124966334 12496633 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
124966334 12496633 Arthritis
124966334 12496633 Diarrhoea
124966334 12496633 Drug intolerance
124966334 12496633 Eye disorder
124966334 12496633 Infection
124966334 12496633 Lower respiratory tract infection
124966334 12496633 Tongue injury
124966334 12496633 Tuberculosis

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
124966334 12496633 1 2013 2014 0