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
125301031 12530103 1 I 20150118 20150120 20160706 20160706 EXP PHHY2015IL008064 NOVARTIS 79.05 YR M Y 93.40000 KG 20160706 CN COUNTRY NOT SPECIFIED IL

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
125301031 12530103 1 PS TASIGNA NILOTINIB 1 Oral 200 MG, BID U SO086, SO122 22068 200 MG CAPSULE BID
125301031 12530103 2 C FUSID FUROSEMIDE 1 Unknown 1 DF, UNK (1 PILL) Y 0 1 DF
125301031 12530103 3 C FUSID FUROSEMIDE 1 Unknown 0.5 DF, UNK (HALF PILL) Y 0 .5 DF
125301031 12530103 4 C HUMALOG MIX INSULIN LISPRO 1 Unknown Y 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
125301031 12530103 1 Chronic myeloid leukaemia
125301031 12530103 2 Renal failure
125301031 12530103 4 Type 2 diabetes mellitus

Outcome of event

Event ID CASEID OUTC COD
125301031 12530103 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
125301031 12530103 Allergic cough
125301031 12530103 Asthenia
125301031 12530103 Cough
125301031 12530103 Dyspnoea
125301031 12530103 Pneumonia
125301031 12530103 Rhinitis allergic

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
125301031 12530103 1 20141008 0