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
121778423 12177842 3 F 20160708 20160314 20160714 EXP US-ALEXION PHARMACEUTICALS INC-A201601625 ALEXION 0.00 M Y 0.00000 20160714 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
121778423 12177842 1 PS SOLIRIS ECULIZUMAB 1 Intravenous (not otherwise specified) UNK U 125166 CONCENTRATE FOR SOLUTION FOR INFUSION

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
121778423 12177842 1 Paroxysmal nocturnal haemoglobinuria

Outcome of event

Event ID CASEID OUTC COD
121778423 12177842 HO

Reactions reported

Event ID CASEID DRUG REC ACT PT
121778423 12177842 Abdominal distension
121778423 12177842 Abdominal tenderness
121778423 12177842 Blood creatinine increased
121778423 12177842 Chromaturia
121778423 12177842 Hypertension
121778423 12177842 Nausea
121778423 12177842 Peripheral swelling
121778423 12177842 Renal disorder
121778423 12177842 Urine output decreased
121778423 12177842 Vomiting
121778423 12177842 Weight increased

Reporting Sources (this data is often not reported and may therefore be missing here)

no results found

Therapies reported

no results found