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
125356332 12535633 2 F 201606 20160802 20160707 20160811 EXP US-ALEXION PHARMACEUTICALS INC-A201604898 ALEXION 73.48 YR F Y 0.00000 20160811 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
125356332 12535633 1 PS SOLIRIS ECULIZUMAB 1 Intravenous (not otherwise specified) 900 MG, Q2W Y 125166 900 MG CONCENTRATE FOR SOLUTION FOR INFUSION QOW

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
125356332 12535633 1 Paroxysmal nocturnal haemoglobinuria

Outcome of event

Event ID CASEID OUTC COD
125356332 12535633 HO
125356332 12535633 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
125356332 12535633 Blood pressure abnormal
125356332 12535633 Cough
125356332 12535633 Dizziness
125356332 12535633 Fatigue
125356332 12535633 Haemoglobin decreased
125356332 12535633 Haemorrhage
125356332 12535633 Nasopharyngitis
125356332 12535633 Pallor

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
125356332 12535633 1 20100211 20160623 0