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
126295761 12629576 1 I 20160726 20160808 20160808 EXP BR-ALEXION PHARMACEUTICALS INC.-A201605625 ALEXION 31.00 YR F Y 0.00000 20160808 CN BR BR

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
126295761 12629576 1 PS SOLIRIS ECULIZUMAB 1 Intravenous (not otherwise specified) 600 MG, QW P0004102 125166 600 MG CONCENTRATE FOR SOLUTION FOR INFUSION /wk
126295761 12629576 2 SS SOLIRIS ECULIZUMAB 1 Intravenous (not otherwise specified) 900 MG, EVERY 15 DAYS P0004102 125166 900 MG CONCENTRATE FOR SOLUTION FOR INFUSION

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
126295761 12629576 1 Paroxysmal nocturnal haemoglobinuria

Outcome of event

Event ID CASEID OUTC COD
126295761 12629576 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
126295761 12629576 Blood lactate dehydrogenase abnormal
126295761 12629576 Drug ineffective
126295761 12629576 Haemoglobin decreased
126295761 12629576 Incorrect product storage
126295761 12629576 Reticulocyte count increased

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
126295761 12629576 1 20120619 0