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
124558895 12455889 5 F 20160811 20160610 20160822 EXP PHHY2016ZA073413 NOVARTIS 0.00 F Y 0.00000 20160822 MD ZA ZA

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
124558895 12455889 1 PS TASIGNA NILOTINIB 1 Oral 200 MG, UNK 22068 200 MG CAPSULE
124558895 12455889 2 SS TASIGNA NILOTINIB 1 Oral 400 MG, UNK 22068 400 MG CAPSULE
124558895 12455889 3 SS TASIGNA NILOTINIB 1 Oral 300 MG, UNK 22068 300 MG CAPSULE
124558895 12455889 4 SS TASIGNA NILOTINIB 1 Oral 1 X 200 MG AM AND 2X200 MG PM (600 MG), QD 22068 600 MG CAPSULE QD
124558895 12455889 5 C SLOW K POTASSIUM CHLORIDE 1 Unknown U 0
124558895 12455889 6 C MAGNESIUM MAGNESIUM 1 Unknown U 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
124558895 12455889 1 Chronic myeloid leukaemia
124558895 12455889 5 Product used for unknown indication
124558895 12455889 6 Product used for unknown indication

Outcome of event

Event ID CASEID OUTC COD
124558895 12455889 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
124558895 12455889 Dry eye
124558895 12455889 Dry skin
124558895 12455889 Feeling hot
124558895 12455889 Gout
124558895 12455889 Pain
124558895 12455889 Peripheral swelling
124558895 12455889 Skin disorder
124558895 12455889 Tenderness
124558895 12455889 Thrombosis

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
124558895 12455889 1 201511 0