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
122391724 12239172 4 F 20160726 20160405 20160803 EXP US-ALEXION PHARMACEUTICALS INC-A201602278 ALEXION 0.00 M Y 0.00000 20160803 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
122391724 12239172 1 PS SOLIRIS ECULIZUMAB 1 Intravenous (not otherwise specified) UNK T3-AE4582B02 125166 CONCENTRATE FOR SOLUTION FOR INFUSION
122391724 12239172 2 SS SOLIRIS ECULIZUMAB 1 Intravenous (not otherwise specified) 900 MG, Q2W 125166 900 MG CONCENTRATE FOR SOLUTION FOR INFUSION QOW

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
122391724 12239172 1 Paroxysmal nocturnal haemoglobinuria

Outcome of event

Event ID CASEID OUTC COD
122391724 12239172 LT
122391724 12239172 OT
122391724 12239172 DE

Reactions reported

Event ID CASEID DRUG REC ACT PT
122391724 12239172 Drug ineffective
122391724 12239172 Immune thrombocytopenic purpura
122391724 12239172 Neutropenia
122391724 12239172 Thrombocytopenia

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
122391724 12239172 1 20160208 0
122391724 12239172 2 20160519 0