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
115514194 11551419 4 F 20150910 20160801 20150925 20160811 EXP US-ALEXION PHARMACEUTICALS INC-A201503606 ALEXION 27.72 YR M Y 0.00000 20160811 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
115514194 11551419 1 PS SOLIRIS ECULIZUMAB 1 Intravenous (not otherwise specified) 900 MG, Q2W 45731.9297 MG N T2-AD9022B02 125166 900 MG CONCENTRATE FOR SOLUTION FOR INFUSION QOW
115514194 11551419 2 C TACROLIMUS. TACROLIMUS 1 Unknown UNK 0
115514194 11551419 3 C FOLIC ACID. FOLIC ACID 1 Unknown UNK 0
115514194 11551419 4 C LOVENOX ENOXAPARIN SODIUM 1 Unknown UNK 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
115514194 11551419 1 Paroxysmal nocturnal haemoglobinuria
115514194 11551419 2 Product used for unknown indication
115514194 11551419 3 Product used for unknown indication
115514194 11551419 4 Product used for unknown indication

Outcome of event

Event ID CASEID OUTC COD
115514194 11551419 HO
115514194 11551419 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
115514194 11551419 Aplastic anaemia
115514194 11551419 Bone marrow failure
115514194 11551419 Condition aggravated
115514194 11551419 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
115514194 11551419 1 20130918 20160609 0