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
121739392 12173939 2 F 20160810 20160314 20160817 EXP US-ALEXION PHARMACEUTICALS INC-A201601581 ALEXION 0.00 M Y 0.00000 20160817 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
121739392 12173939 1 PS SOLIRIS ECULIZUMAB 1 Intravenous (not otherwise specified) N T3-AE3114B04 125166 CONCENTRATE FOR SOLUTION FOR INFUSION
121739392 12173939 2 C CYCLOSPORINE. CYCLOSPORINE 1 Unknown 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
121739392 12173939 1 Haemolytic uraemic syndrome
121739392 12173939 2 Product used for unknown indication

Outcome of event

Event ID CASEID OUTC COD
121739392 12173939 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
121739392 12173939 Aggression
121739392 12173939 Blood pressure fluctuation
121739392 12173939 Depression
121739392 12173939 Feeling abnormal
121739392 12173939 Gout
121739392 12173939 Insomnia
121739392 12173939 Morbid thoughts
121739392 12173939 Pain
121739392 12173939 Sleep disorder
121739392 12173939 Suicidal ideation

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

no results found

Therapies reported

no results found