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
111696663 11169666 3 F 20140925 20160818 20150605 20160923 EXP PHHY2015KR061552 NOVARTIS 56.47 YR F Y 0.00000 20160923 MD KR KR

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
111696663 11169666 1 PS TASIGNA NILOTINIB 1 Oral 400 MG, QD 11200 MG 22068 400 MG CAPSULE QD
111696663 11169666 2 SS TASIGNA NILOTINIB 1 Oral 600 MG, QD 11200 MG 22068 600 MG CAPSULE QD
111696663 11169666 3 C OFAL//OFLOXACIN 2 Ophthalmic 2 DF, UNK Y 0 2 DF
111696663 11169666 4 C HYALURONATE NA 2 Ophthalmic 0.4 ML, UNK Y 0 .4 ML
111696663 11169666 5 C ALBIS BISMUTH SUBCITRATERANITIDINE HYDROCHLORIDESUCRALFATE 1 Oral 1 DF, UNK Y 0 1 DF TABLET

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
111696663 11169666 1 Chronic myeloid leukaemia
111696663 11169666 3 Blepharitis
111696663 11169666 4 Blepharitis
111696663 11169666 5 Abdominal pain upper

Outcome of event

no results found

Reactions reported

Event ID CASEID DRUG REC ACT PT
111696663 11169666 Alopecia
111696663 11169666 Arthralgia
111696663 11169666 Rash

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
111696663 11169666 1 20140529 20140625 0
111696663 11169666 2 20140626 0
111696663 11169666 3 20121128 20140728 0
111696663 11169666 4 20121128 20140728 0
111696663 11169666 5 20140529 20140625 0