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
125798671 12579867 1 I 20160630 20160721 20160721 EXP PHHY2016CO091458 NOVARTIS 0.00 F Y 51.00000 KG 20160721 CN COUNTRY NOT SPECIFIED CO

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
125798671 12579867 1 PS TASIGNA NILOTINIB 1 Oral 150 MG, Q12H U 22068 150 MG CAPSULE Q12H
125798671 12579867 2 C AMOXICILLIN. AMOXICILLIN 1 Oral 500 MG, TID U 0 500 MG CAPSULE TID
125798671 12579867 3 C IBUPROFEN. IBUPROFEN 1 Oral 250 MG, TID U 0 250 MG TABLET TID
125798671 12579867 4 C ADVIL IBUPROFEN 1 Oral PRN U 0 TABLET

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
125798671 12579867 1 Chronic myeloid leukaemia
125798671 12579867 2 Tonsillitis
125798671 12579867 3 Pain
125798671 12579867 4 Product used for unknown indication

Outcome of event

no results found

Reactions reported

Event ID CASEID DRUG REC ACT PT
125798671 12579867 Diarrhoea
125798671 12579867 Dizziness
125798671 12579867 Food interaction
125798671 12579867 Headache

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
125798671 12579867 1 20160622 0