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
126027611 12602761 1 I 20160718 20160728 20160728 PER US-ALEXION PHARMACEUTICALS INC-A201605370 ALEXION 0.00 M Y 0.00000 20160728 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
126027611 12602761 1 PS SOLIRIS ECULIZUMAB 1 Intravenous (not otherwise specified) UNK U 125166 CONCENTRATE FOR SOLUTION FOR INFUSION
126027611 12602761 2 SS MESALAMINE. MESALAMINE 1 Unknown UNK U 0
126027611 12602761 3 C VITAMIN B12 CYANOCOBALAMIN 1 Unknown UNK, Q4WEEKS 0
126027611 12602761 4 C IRON IRON 1 Unknown UNK 0
126027611 12602761 5 C PROCRIT ERYTHROPOIETIN 1 Unknown UNK, Q2W 0 QOW

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
126027611 12602761 1 Paroxysmal nocturnal haemoglobinuria
126027611 12602761 2 Crohn's disease
126027611 12602761 3 Product used for unknown indication
126027611 12602761 4 Product used for unknown indication
126027611 12602761 5 Product used for unknown indication

Outcome of event

Event ID CASEID OUTC COD
126027611 12602761 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
126027611 12602761 Anaemia
126027611 12602761 Dyspnoea
126027611 12602761 Fatigue

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

no results found

Therapies reported

no results found