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
126446513 12644651 3 F 2016 20160922 20160811 20160930 EXP US-ALEXION PHARMACEUTICALS INC.-A201605748 ALEXION 28.74 YR M Y 0.00000 20160930 CN US US

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
126446513 12644651 1 PS SOLIRIS ECULIZUMAB 1 Intravenous (not otherwise specified) 900 MG, UNK U 125166 900 MG CONCENTRATE FOR SOLUTION FOR INFUSION
126446513 12644651 2 SS SOLIRIS ECULIZUMAB 1 Intravenous (not otherwise specified) 900 MG, EVERY 10 DAYS U 125166 900 MG CONCENTRATE FOR SOLUTION FOR INFUSION

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
126446513 12644651 1 Paroxysmal nocturnal haemoglobinuria

Outcome of event

Event ID CASEID OUTC COD
126446513 12644651 OT
126446513 12644651 HO

Reactions reported

Event ID CASEID DRUG REC ACT PT
126446513 12644651 Abdominal pain
126446513 12644651 Chromaturia
126446513 12644651 Device related thrombosis
126446513 12644651 Inappropriate schedule of drug administration
126446513 12644651 Jugular vein thrombosis
126446513 12644651 Superior sagittal sinus thrombosis

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
126446513 12644651 1 201410 0