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
109619153 10961915 3 F 20141006 20160727 20150327 20160808 EXP PHHY2014DE137956 NOVARTIS 0.00 E F Y 0.00000 20160808 MD DE DE

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
109619153 10961915 1 PS TASIGNA NILOTINIB 1 Oral 600 MG, QD U 22068 600 MG CAPSULE QD
109619153 10961915 2 C PANTOPRAZOL PANTOPRAZOLE SODIUM 1 Unknown 40 MG, UNK 0 40 MG
109619153 10961915 3 C CIPROFLOXACIN. CIPROFLOXACIN 1 Unknown 500 MG/1000 MG, QD 5000 MG Y 0 1000 MG QD

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
109619153 10961915 1 Chronic myeloid leukaemia
109619153 10961915 2 Product used for unknown indication
109619153 10961915 3 Product used for unknown indication

Outcome of event

no results found

Reactions reported

Event ID CASEID DRUG REC ACT PT
109619153 10961915 Nasopharyngitis
109619153 10961915 Productive cough
109619153 10961915 Pruritus
109619153 10961915 Seborrhoea

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
109619153 10961915 1 20140801 0
109619153 10961915 2 20140723 0
109619153 10961915 3 20141006 20141010 0