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
124866902 12486690 2 F 2013 20160726 20160621 20160803 EXP TR-ALEXION-A201502638 ALEXION 32.76 YR F Y 58.00000 KG 20160803 CN TR TR

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
124866902 12486690 1 PS SOLIRIS ECULIZUMAB 1 Intravenous (not otherwise specified) 900 MG, Q2W 125166 900 MG CONCENTRATE FOR SOLUTION FOR INFUSION QOW
124866902 12486690 2 C IRON IRON 1 Unknown 0
124866902 12486690 3 C MULTIVITAMIN /00097801/ VITAMINS 1 Unknown 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
124866902 12486690 1 Paroxysmal nocturnal haemoglobinuria
124866902 12486690 2 Product used for unknown indication
124866902 12486690 3 Product used for unknown indication

Outcome of event

Event ID CASEID OUTC COD
124866902 12486690 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
124866902 12486690 Exposure during pregnancy
124866902 12486690 Incorrect dose administered
124866902 12486690 Respiratory distress

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
124866902 12486690 1 2013 0