The Safety Rates Drug Report

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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
124118522 12411852 2 F 20151022 20160818 20160527 20160923 EXP PHHY2016KR070366 NOVARTIS 69.22 YR M 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
124118522 12411852 1 PS TASIGNA NILOTINIB 1 Oral 600 MG, QD (PER DAY) 22068 600 MG CAPSULE QD
124118522 12411852 2 C TACROLIMUS. TACROLIMUS 1 Oral 0.5 MG, UNK 0 .5 MG
124118522 12411852 3 C TACROLIMUS. TACROLIMUS 1 Oral 0.25 MG, UNK 0 .25 MG
124118522 12411852 4 C UDCA URSODIOL 1 Oral 600 MG, UNK 0 600 MG
124118522 12411852 5 C LORAZEPAM. LORAZEPAM 1 Intravenous (not otherwise specified) 2 MG, UNK Y 0 2 MG

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
124118522 12411852 1 Chronic myeloid leukaemia
124118522 12411852 2 Prophylaxis against transplant rejection
124118522 12411852 4 Prophylaxis
124118522 12411852 5 Prophylaxis

Outcome of event

no results found

Reactions reported

Event ID CASEID DRUG REC ACT PT
124118522 12411852 Conjunctival hyperaemia
124118522 12411852 Dyspnoea
124118522 12411852 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
124118522 12411852 1 20150925 0
124118522 12411852 2 20150203 20151130 0
124118522 12411852 3 20151201 0
124118522 12411852 4 20100629 0
124118522 12411852 5 20160317 20160317 0