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
127081182 12708118 2 F 20160909 20160909 20160901 20160916 EXP GB-ALEXION PHARMACEUTICALS INC.-A201606432 ALEXION 31.37 YR F Y 0.00000 20160916 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
127081182 12708118 1 PS SOLIRIS ECULIZUMAB 1 Intravenous (not otherwise specified) UNK, QW 125166 CONCENTRATE FOR SOLUTION FOR INFUSION /wk
127081182 12708118 2 SS SOLIRIS ECULIZUMAB 1 Intravenous (not otherwise specified) 900 MG, Q2W 125166 900 MG CONCENTRATE FOR SOLUTION FOR INFUSION QOW

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
127081182 12708118 1 Paroxysmal nocturnal haemoglobinuria

Outcome of event

Event ID CASEID OUTC COD
127081182 12708118 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
127081182 12708118 Dyspnoea exertional
127081182 12708118 Fatigue
127081182 12708118 Haemoglobin decreased
127081182 12708118 Hypotension
127081182 12708118 Lower respiratory tract infection

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
127081182 12708118 1 20100603 20120419 0
127081182 12708118 2 20120419 0