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
120954062 12095406 2 F 20130629 20160831 20160219 20160911 EXP JP-ALEXION PHARMACEUTICALS INC-A201600778 ALEXION 33.00 YR F Y 0.00000 20160911 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
120954062 12095406 1 PS SOLIRIS ECULIZUMAB 1 Intravenous (not otherwise specified) 600 MG, QW 125166 600 MG CONCENTRATE FOR SOLUTION FOR INFUSION /wk
120954062 12095406 2 SS SOLIRIS ECULIZUMAB 1 Intravenous (not otherwise specified) 900 MG, Q2W 125166 900 MG CONCENTRATE FOR SOLUTION FOR INFUSION QOW
120954062 12095406 3 C HEPARIN CALCIUM HEPARIN CALCIUM 1 Subcutaneous 10000 IU, QD 0 10000 IU QD

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
120954062 12095406 1 Paroxysmal nocturnal haemoglobinuria
120954062 12095406 3 Thrombosis

Outcome of event

Event ID CASEID OUTC COD
120954062 12095406 OT
120954062 12095406 HO

Reactions reported

Event ID CASEID DRUG REC ACT PT
120954062 12095406 Exposure during pregnancy
120954062 12095406 Haemoglobin decreased
120954062 12095406 Premature rupture of membranes
120954062 12095406 Small size placenta
120954062 12095406 Umbilical cord abnormality

Reporting Sources (this data is often not reported and may therefore be missing here)

no results found

Therapies reported

no results found