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
118133366 11813336 6 F 20150810 20160826 20151209 20160830 EXP CA-ROCHE-1617771 ROCHE 15.76 YR F Y 50.40000 KG 20160831 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
118133366 11813336 1 PS ACTEMRA TOCILIZUMAB 1 Intravenous (not otherwise specified) N B2049,B2036,B20470,B2039,B2048 125276 380 MG SOLUTION FOR INFUSION
118133366 11813336 2 SS ACTEMRA TOCILIZUMAB 1 Intravenous (not otherwise specified) N B2049,B2036,B20470,B2039,B2048 125276 360 MG SOLUTION FOR INFUSION
118133366 11813336 3 SS ACTEMRA TOCILIZUMAB 1 Intravenous (not otherwise specified) N B2049,B2036,B20470,B2039,B2048 125276 360 MG SOLUTION FOR INFUSION Q3W
118133366 11813336 4 C PREDNISONE. PREDNISONE 1 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
118133366 11813336 1 Juvenile idiopathic arthritis

Outcome of event

Event ID CASEID OUTC COD
118133366 11813336 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
118133366 11813336 Hypotension
118133366 11813336 Lymphocyte count decreased
118133366 11813336 Neutrophil count abnormal
118133366 11813336 Neutrophil count decreased
118133366 11813336 Weight increased
118133366 11813336 White blood cell count decreased

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
118133366 11813336 1 20150706 0
118133366 11813336 2 20151109 0
118133366 11813336 3 20160302 0