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
124765992 12476599 2 F 20160404 20160801 20160617 20160805 EXP PHHY2013LB040757 NOVARTIS 33.49 YR M Y 0.00000 20160805 MD LB LB

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
124765992 12476599 1 PS TASIGNA NILOTINIB 1 Oral 800 MG, QD U 22068 800 MG CAPSULE QD
124765992 12476599 2 C EPANUTIN PHENYTOIN SODIUM 1 Oral U 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
124765992 12476599 1 Chronic myeloid leukaemia
124765992 12476599 2 Product used for unknown indication

Outcome of event

Event ID CASEID OUTC COD
124765992 12476599 HO
124765992 12476599 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
124765992 12476599 Blood potassium decreased
124765992 12476599 Cerebral haemorrhage
124765992 12476599 Dizziness
124765992 12476599 Exposure via father
124765992 12476599 Headache
124765992 12476599 Influenza
124765992 12476599 Intracranial aneurysm
124765992 12476599 Pyrexia
124765992 12476599 Wound complication

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
124765992 12476599 1 20130130 0
124765992 12476599 2 201607 0