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
125238451 12523845 1 I 20160624 20160704 20160704 EXP US-ALEXION PHARMACEUTICALS INC-A201604833 ALEXION 21.00 YR F Y 0.00000 20160704 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
125238451 12523845 1 PS SOLIRIS ECULIZUMAB 1 Intravenous (not otherwise specified) 900 MG, Q2W U 125166 900 MG CONCENTRATE FOR SOLUTION FOR INFUSION QOW
125238451 12523845 2 SS SOLIRIS ECULIZUMAB 1 Intravenous (not otherwise specified) 1200 MG, Q2W U 125166 1200 MG CONCENTRATE FOR SOLUTION FOR INFUSION QOW
125238451 12523845 3 SS SOLIRIS ECULIZUMAB 1 Intravenous (not otherwise specified) 900 MG, Q2W U 125166 900 MG CONCENTRATE FOR SOLUTION FOR INFUSION QOW

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
125238451 12523845 1 Paroxysmal nocturnal haemoglobinuria

Outcome of event

Event ID CASEID OUTC COD
125238451 12523845 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
125238451 12523845 Exposure during pregnancy
125238451 12523845 Granulocyte count decreased
125238451 12523845 Haemolysis
125238451 12523845 Incorrect dose administered
125238451 12523845 Platelet count decreased
125238451 12523845 Thrombosis
125238451 12523845 White blood cell count decreased

Reporting Sources (this data is often not reported and may therefore be missing here)

no results found

Therapies reported

no results found