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
115889438 11588943 8 F 201505 20160715 20151002 20160726 EXP AU-ALEXION PHARMACEUTICALS INC-A201503775 ALEXION 63.12 YR F Y 0.00000 20160726 CN AU AU

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
115889438 11588943 1 PS SOLIRIS ECULIZUMAB 1 Intravenous (not otherwise specified) 900 MG, Q2W 125166 900 MG CONCENTRATE FOR SOLUTION FOR INFUSION QOW
115889438 11588943 2 C ZOLOFT SERTRALINE HYDROCHLORIDE 1 Unknown 100 MG, BID 0 100 MG BID
115889438 11588943 3 C ISOPTIN VERAPAMIL HYDROCHLORIDE 1 Unknown 240 MG, BID 0 240 MG BID
115889438 11588943 4 C ATACAND PLUS CANDESARTAN CILEXETILHYDROCHLOROTHIAZIDE 1 Unknown UNK, BID, 16/12.5 0 BID
115889438 11588943 5 C SPIRONOLACTONE. SPIRONOLACTONE 1 Unknown 25 MG, QD 0 25 MG QD
115889438 11588943 6 C ALLOPURINOL. ALLOPURINOL 1 Unknown 300 MG, QD 0 300 MG QD
115889438 11588943 7 C AMITRIPTYLINE AMITRIPTYLINE 1 Unknown 25 MG, AT NIGHT 0 25 MG
115889438 11588943 8 C FOLIC ACID. FOLIC ACID 1 Unknown 5 MG, QD 0 5 MG QD

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
115889438 11588943 1 Paroxysmal nocturnal haemoglobinuria
115889438 11588943 2 Product used for unknown indication
115889438 11588943 3 Product used for unknown indication
115889438 11588943 4 Product used for unknown indication
115889438 11588943 5 Product used for unknown indication
115889438 11588943 6 Product used for unknown indication
115889438 11588943 7 Product used for unknown indication
115889438 11588943 8 Product used for unknown indication

Outcome of event

Event ID CASEID OUTC COD
115889438 11588943 HO
115889438 11588943 DE
115889438 11588943 OT
115889438 11588943 LT

Reactions reported

Event ID CASEID DRUG REC ACT PT
115889438 11588943 Back pain
115889438 11588943 Cancer pain
115889438 11588943 Loss of consciousness
115889438 11588943 Pain
115889438 11588943 Pancreatic carcinoma
115889438 11588943 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
115889438 11588943 1 201105 0