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
119910594 11991059 4 F 20160117 20160628 20160202 20160707 EXP GB-ALEXION-A201600552 ALEXION 40.23 YR F Y 0.00000 20160707 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
119910594 11991059 1 PS SOLIRIS ECULIZUMAB 1 Intravenous (not otherwise specified) 900 MG, Q2W P0003801 125166 900 MG CONCENTRATE FOR SOLUTION FOR INFUSION QOW
119910594 11991059 2 C CIPROFLOXACIN. CIPROFLOXACIN 1 Unknown 0
119910594 11991059 3 C CIPROFLOXACIN. CIPROFLOXACIN 1 0
119910594 11991059 4 C NYSTATIN. NYSTATIN 1 Unknown 0
119910594 11991059 5 C NYSTATIN. NYSTATIN 1 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
119910594 11991059 1 Paroxysmal nocturnal haemoglobinuria
119910594 11991059 2 Leukaemia
119910594 11991059 3 Neutropenia
119910594 11991059 4 Leukaemia
119910594 11991059 5 Neutropenia

Outcome of event

Event ID CASEID OUTC COD
119910594 11991059 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
119910594 11991059 Device issue
119910594 11991059 Dysphagia
119910594 11991059 Fatigue
119910594 11991059 Hypotension
119910594 11991059 Leukaemia
119910594 11991059 Oral pain
119910594 11991059 Red blood cell count decreased

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
119910594 11991059 1 20101209 0