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
120720154 12072015 4 F 20140122 20160915 20160212 20160919 EXP CA-ROCHE-1339283 ROCHE 32.59 YR F Y 102.00000 KG 20160919 OT 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
120720154 12072015 1 PS ACTEMRA TOCILIZUMAB 1 Intravenous (not otherwise specified) B2062 125276 800 MG SOLUTION FOR INFUSION
120720154 12072015 2 C SYMBICORT BUDESONIDEFORMOTEROL FUMARATE DIHYDRATE 1 0
120720154 12072015 3 C LEFLUNOMIDE. LEFLUNOMIDE 1 0
120720154 12072015 4 C REMICADE INFLIXIMAB 1 0
120720154 12072015 5 C HYDROXYCHLOROQUINE HYDROXYCHLOROQUINE 1 0
120720154 12072015 6 C PREDNISONE. PREDNISONE 1 0
120720154 12072015 7 C ARTHROTEC DICLOFENAC SODIUMMISOPROSTOL 1 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
120720154 12072015 1 Rheumatoid arthritis

Outcome of event

Event ID CASEID OUTC COD
120720154 12072015 HO

Reactions reported

Event ID CASEID DRUG REC ACT PT
120720154 12072015 Appendix disorder
120720154 12072015 Blood pressure increased
120720154 12072015 Heart rate increased
120720154 12072015 Infusion related reaction
120720154 12072015 Weight increased

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
120720154 12072015 1 20140122 0