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
124543212 12454321 2 F 20160530 20160809 20160610 20160817 EXP CO-ALEXION PHARMACEUTICALS INC-A201604238 ALEXION 19.00 YR F Y 0.00000 20160817 CN CO CO

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
124543212 12454321 1 PS SOLIRIS ECULIZUMAB 1 Intravenous (not otherwise specified) 900 MG, QW 125166 900 MG CONCENTRATE FOR SOLUTION FOR INFUSION /wk
124543212 12454321 2 SS SOLIRIS ECULIZUMAB 1 Intravenous (not otherwise specified) 1200 MG, Q2W AE1235B05 125166 1200 MG CONCENTRATE FOR SOLUTION FOR INFUSION QOW

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
124543212 12454321 1 Haemolytic uraemic syndrome

Outcome of event

Event ID CASEID OUTC COD
124543212 12454321 HO
124543212 12454321 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
124543212 12454321 Fatigue
124543212 12454321 Haemoglobin decreased
124543212 12454321 Inappropriate schedule of drug administration
124543212 12454321 Platelet 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
124543212 12454321 1 20150730 20150820 0
124543212 12454321 2 20150903 0