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
124623193 12462319 3 F 20160602 20160708 20160613 20160714 EXP JP-ALXN-A201604204AA ALEXION 4.00 DEC F Y 0.00000 20160714 MD JP JP

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
124623193 12462319 1 PS SOLIRIS ECULIZUMAB 1 Intravenous (not otherwise specified) 900 MG, QW 257.143005 MG AE5436B01 125166 900 MG CONCENTRATE FOR SOLUTION FOR INFUSION /wk
124623193 12462319 2 SS SOLIRIS ECULIZUMAB 1 Intravenous (not otherwise specified) 1200 MG, Q2W 257.143005 MG 125166 1200 MG CONCENTRATE FOR SOLUTION FOR INFUSION QOW

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
124623193 12462319 1 Haemolytic uraemic syndrome

Outcome of event

Event ID CASEID OUTC COD
124623193 12462319 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
124623193 12462319 Cardiac failure
124623193 12462319 Drug ineffective
124623193 12462319 Haemoglobin decreased
124623193 12462319 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
124623193 12462319 1 20160601 20160628 0
124623193 12462319 2 20160629 0