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
116079432 11607943 2 F 20150831 20160921 20151007 20160929 EXP PHHY2015DE120482 NOVARTIS 0.00 E F Y 0.00000 20160929 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
116079432 11607943 1 PS TASIGNA NILOTINIB 1 Oral 600 MG, QD 5400 MG D 22068 600 MG CAPSULE QD
116079432 11607943 2 C SALBUTAMOL ALBUTEROL 1 Unknown UNK 0
116079432 11607943 3 C OMEPRAZOL//OMEPRAZOLE 2 Unknown UNK D 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
116079432 11607943 1 Chronic myeloid leukaemia
116079432 11607943 2 Emphysema
116079432 11607943 3 Dyspepsia

Outcome of event

no results found

Reactions reported

Event ID CASEID DRUG REC ACT PT
116079432 11607943 Anaemia
116079432 11607943 Bronchitis

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
116079432 11607943 1 20150219 20150227 0
116079432 11607943 2 20141211 0
116079432 11607943 3 20150228 20150319 0