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
124366384 12436638 4 F 20160715 20160606 20160726 EXP US-ALEXION-A201604022 ALEXION 0.00 F Y 0.00000 20160726 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
124366384 12436638 1 PS SOLIRIS ECULIZUMAB 1 Intravenous (not otherwise specified) 900 MG, UNK U 125166 900 MG CONCENTRATE FOR SOLUTION FOR INFUSION
124366384 12436638 2 SS 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
124366384 12436638 1 Paroxysmal nocturnal haemoglobinuria

Outcome of event

Event ID CASEID OUTC COD
124366384 12436638 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
124366384 12436638 Asthenia
124366384 12436638 Blood glucose increased
124366384 12436638 Blood lactate dehydrogenase increased
124366384 12436638 Dyspnoea
124366384 12436638 Dyspnoea exertional
124366384 12436638 Fatigue
124366384 12436638 Haemoglobin decreased
124366384 12436638 Hyperhidrosis
124366384 12436638 Muscle spasms

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
124366384 12436638 1 20140912 20160429 0
124366384 12436638 2 20160610 0