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
119371042 11937104 2 F 20160105 20160824 20160121 20160830 EXP US-ALEXION PHARMACEUTICALS INC-A201600269 ALEXION 0.00 F Y 0.00000 20160830 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
119371042 11937104 1 PS SOLIRIS ECULIZUMAB 1 Intravenous (not otherwise specified) 900 MG, Q2W 160973.547 MG T2-AE3114B04 125166 900 MG CONCENTRATE FOR SOLUTION FOR INFUSION QOW
119371042 11937104 2 SS SOLIRIS ECULIZUMAB 1 Intravenous (not otherwise specified) 900 MG, Q2W 160973.547 MG T2-AE1225B01 125166 900 MG CONCENTRATE FOR SOLUTION FOR INFUSION QOW
119371042 11937104 3 C DANAZOL. DANAZOL 1 Oral 200 MG, UNK 0 200 MG

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
119371042 11937104 1 Paroxysmal nocturnal haemoglobinuria
119371042 11937104 3 Paroxysmal nocturnal haemoglobinuria

Outcome of event

Event ID CASEID OUTC COD
119371042 11937104 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
119371042 11937104 Haemoglobin decreased

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
119371042 11937104 1 20090116 0
119371042 11937104 2 20090116 20160816 0
119371042 11937104 3 20160822 0