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
113171273 11317127 3 F 20140408 20160630 20150728 20160708 EXP JP-ALEXION-A201401173 ALEXION 74.00 YR M Y 57.00000 KG 20160708 MD JP JP

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
113171273 11317127 1 PS SOLIRIS ECULIZUMAB 1 Intravenous (not otherwise specified) 600 MG, QW 125166 600 MG CONCENTRATE FOR SOLUTION FOR INFUSION /wk
113171273 11317127 2 SS SOLIRIS ECULIZUMAB 1 Intravenous (not otherwise specified) 900 MG, Q2W AA8793B01 125166 900 MG CONCENTRATE FOR SOLUTION FOR INFUSION QOW
113171273 11317127 3 C PREDNISOLON /00016201/ PREDNISOLONE 1 Unknown 10 MG, DAILY 0 10 MG QD

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
113171273 11317127 1 Paroxysmal nocturnal haemoglobinuria
113171273 11317127 3 Paroxysmal nocturnal haemoglobinuria

Outcome of event

Event ID CASEID OUTC COD
113171273 11317127 HO
113171273 11317127 OT
113171273 11317127 LT

Reactions reported

Event ID CASEID DRUG REC ACT PT
113171273 11317127 Anaemia
113171273 11317127 C-reactive protein increased
113171273 11317127 Small intestine carcinoma

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
113171273 11317127 1 20130813 20130903 0
113171273 11317127 2 20130910 0
113171273 11317127 3 20130713 0