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
127271191 12727119 1 I 20160526 20160909 20160909 EXP GB-ALEXION PHARMACEUTICALS INC.-A201604083 ALEXION 0.00 F Y 0.00000 20160909 CN GB GB

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
127271191 12727119 1 PS SOLIRIS ECULIZUMAB 1 Intravenous (not otherwise specified) UNK 125166 CONCENTRATE FOR SOLUTION FOR INFUSION
127271191 12727119 2 SS SOLIRIS ECULIZUMAB 1 Intravenous (not otherwise specified) 1200 MG, Q2W P0004707 125166 1200 MG CONCENTRATE FOR SOLUTION FOR INFUSION QOW
127271191 12727119 3 SS SOLIRIS ECULIZUMAB 1 Intravenous (not otherwise specified) 1200 MG, Q2W P0005002 125166 1200 MG CONCENTRATE FOR SOLUTION FOR INFUSION QOW
127271191 12727119 4 SS SIMVASTATIN. SIMVASTATIN 1 Unknown UNK U 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
127271191 12727119 1 Haemolytic uraemic syndrome
127271191 12727119 4 Product used for unknown indication

Outcome of event

Event ID CASEID OUTC COD
127271191 12727119 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
127271191 12727119 Back pain
127271191 12727119 Chronic obstructive pulmonary disease
127271191 12727119 Dyspnoea
127271191 12727119 Fatigue
127271191 12727119 Hot flush
127271191 12727119 Muscle spasms

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
127271191 12727119 2 20111231 0
127271191 12727119 3 20111231 0