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
126052651 12605265 1 I 20160719 20160720 20160729 20160729 EXP BR-ALEXION PHARMACEUTICALS INC-A201605486 ALEXION 38.66 YR F Y 0.00000 20160729 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
126052651 12605265 1 PS SOLIRIS ECULIZUMAB 1 Intravenous (not otherwise specified) 600 MG, UNK U 125166 600 MG CONCENTRATE FOR SOLUTION FOR INFUSION
126052651 12605265 2 SS SOLIRIS ECULIZUMAB 1 Intravenous (not otherwise specified) 900 MG, UNK U 125166 900 MG CONCENTRATE FOR SOLUTION FOR INFUSION

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
126052651 12605265 1 Paroxysmal nocturnal haemoglobinuria

Outcome of event

Event ID CASEID OUTC COD
126052651 12605265 HO
126052651 12605265 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
126052651 12605265 Abdominal pain
126052651 12605265 Chromaturia
126052651 12605265 Haematuria

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
126052651 12605265 1 20100325 0