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
126169012 12616901 2 F 20160719 20160921 20160802 20160929 EXP PHHY2016CA104108 NOVARTIS 79.00 YR F Y 71.50000 KG 20160929 CN COUNTRY NOT SPECIFIED CA

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
126169012 12616901 1 PS EXJADE DEFERASIROX 1 Oral UNK 21882 DISPERSIBLE TABLET
126169012 12616901 2 SS KEFLEX CEPHALEXIN 1 Unknown UNK 0
126169012 12616901 3 SS KEFLEX CEPHALEXIN 1 0
126169012 12616901 4 SS VITAMIN D CHOLECALCIFEROL 1 Oral UNK 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
126169012 12616901 1 Iron overload
126169012 12616901 2 Groin infection
126169012 12616901 3 Inguinal mass
126169012 12616901 4 Supplementation therapy

Outcome of event

Event ID CASEID OUTC COD
126169012 12616901 HO

Reactions reported

Event ID CASEID DRUG REC ACT PT
126169012 12616901 Electrocardiogram abnormal
126169012 12616901 Myocardial ischaemia
126169012 12616901 Urinary tract infection
126169012 12616901 Ventricular extrasystoles

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
126169012 12616901 1 2014 0
126169012 12616901 2 20160624 0
126169012 12616901 4 2014 0