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
126045461 12604546 1 I 20160711 20160720 20160728 20160728 EXP US-ALEXION PHARMACEUTICALS INC.-A201605433 ALEXION 0.00 F Y 0.00000 20160728 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
126045461 12604546 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
126045461 12604546 1 Paroxysmal nocturnal haemoglobinuria

Outcome of event

Event ID CASEID OUTC COD
126045461 12604546 OT
126045461 12604546 HO

Reactions reported

Event ID CASEID DRUG REC ACT PT
126045461 12604546 Acute kidney injury
126045461 12604546 Anaemia
126045461 12604546 Confusional state
126045461 12604546 Deep vein thrombosis
126045461 12604546 Erythema
126045461 12604546 Haemoglobin decreased
126045461 12604546 Mental status changes
126045461 12604546 Pain in extremity
126045461 12604546 Peripheral swelling
126045461 12604546 Platelet count decreased
126045461 12604546 Skin warm

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

no results found

Therapies reported

no results found