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
121844573 12184457 3 F 20160316 20160711 20160316 20160721 EXP GB-ALEXION PHARMACEUTICALS INC-A201601720 ALEXION 41.32 YR M Y 0.00000 20160721 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
121844573 12184457 1 PS SOLIRIS ECULIZUMAB 1 Intravenous (not otherwise specified) UNK 125166 CONCENTRATE FOR SOLUTION FOR INFUSION
121844573 12184457 2 SS SOLIRIS ECULIZUMAB 1 Intravenous (not otherwise specified) 900 MG, Q2W P0004102 125166 900 MG CONCENTRATE FOR SOLUTION FOR INFUSION QOW

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
121844573 12184457 1 Paroxysmal nocturnal haemoglobinuria

Outcome of event

Event ID CASEID OUTC COD
121844573 12184457 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
121844573 12184457 Asthenia
121844573 12184457 Fatigue
121844573 12184457 Haemolysis
121844573 12184457 Sleep disorder

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
121844573 12184457 2 20151125 0