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
124145732 12414573 2 F 20160912 20160528 20160919 EXP PHEH2014US026021 NOVARTIS 0.00 M Y 0.00000 20160919 CN US US

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
124145732 12414573 1 PS TASIGNA NILOTINIB 1 Unknown 2 DF, BID U F0032 22068 2 DF CAPSULE BID
124145732 12414573 2 SS TASIGNA NILOTINIB 1 Unknown 1 DF, QD U 22068 1 DF CAPSULE QD
124145732 12414573 3 SS TASIGNA NILOTINIB 1 Oral 150 MG, BID U F00406/F0054A 22068 150 MG CAPSULE BID
124145732 12414573 4 C DUETACT GLIMEPIRIDEPIOGLITAZONE HYDROCHLORIDE 1 Unknown U 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
124145732 12414573 1 Chronic myeloid leukaemia
124145732 12414573 4 Type 2 diabetes mellitus

Outcome of event

Event ID CASEID OUTC COD
124145732 12414573 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
124145732 12414573 Blood glucose increased
124145732 12414573 Dyspnoea at rest
124145732 12414573 Palpitations
124145732 12414573 Pruritus
124145732 12414573 Rash
124145732 12414573 Wheezing

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
124145732 12414573 1 20141211 0