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
1043567123 10435671 23 F 20140818 20160921 20140908 20160926 EXP PHHY2014LB106614 NOVARTIS 38.26 YR M Y 0.00000 20160926 MD LB LB

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
1043567123 10435671 1 PS TASIGNA NILOTINIB 1 Oral 600 MG, QD 22068 600 MG CAPSULE QD
1043567123 10435671 2 SS TASIGNA NILOTINIB 1 Oral 300 MG, QD 22068 300 MG CAPSULE QD
1043567123 10435671 3 SS TASIGNA NILOTINIB 1 Oral 450 MG, QD 22068 450 MG CAPSULE QD
1043567123 10435671 4 C ADVIL-CS 2 Oral PRN U 0
1043567123 10435671 5 C ZYLORIC ALLOPURINOL 1 Oral 1 DF, QD U 0 1 DF TABLET QD
1043567123 10435671 6 C GALVUS MET METFORMIN HYDROCHLORIDEVILDAGLIPTIN 1 Oral 1 DF, QD U 0 1 DF TABLET QD
1043567123 10435671 7 C NEXIUM I.V. ESOMEPRAZOLE SODIUM 1 Oral 1 DF, QD Y 0 1 DF TABLET QD
1043567123 10435671 8 C PEPTAZOL PANTOPRAZOLE SODIUM 1 Oral 1 DF, QD U 0 1 DF TABLET QD
1043567123 10435671 9 C ADVIL IBUPROFEN 1 Oral PRN U 0
1043567123 10435671 10 C ADVIL IBUPROFEN 1 U 0
1043567123 10435671 11 C ADVIL IBUPROFEN 1 U 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
1043567123 10435671 1 Chronic myeloid leukaemia
1043567123 10435671 4 Product used for unknown indication
1043567123 10435671 5 Product used for unknown indication
1043567123 10435671 6 Product used for unknown indication
1043567123 10435671 7 Product used for unknown indication
1043567123 10435671 8 Product used for unknown indication
1043567123 10435671 9 Gastroenteritis
1043567123 10435671 10 Pyrexia
1043567123 10435671 11 Chills

Outcome of event

no results found

Reactions reported

Event ID CASEID DRUG REC ACT PT
1043567123 10435671 Abdominal pain
1043567123 10435671 Abdominal pain upper
1043567123 10435671 Alopecia
1043567123 10435671 Arthralgia
1043567123 10435671 Chills
1043567123 10435671 Cytogenetic analysis abnormal
1043567123 10435671 Dermatitis allergic
1043567123 10435671 Dizziness
1043567123 10435671 Erectile dysfunction
1043567123 10435671 Erythema
1043567123 10435671 Exposure via father
1043567123 10435671 Fatigue
1043567123 10435671 Furuncle
1043567123 10435671 Gastroenteritis
1043567123 10435671 Headache
1043567123 10435671 Hyperglycaemia
1043567123 10435671 Hypersensitivity
1043567123 10435671 Hypertension
1043567123 10435671 Hypoglycaemia
1043567123 10435671 Inappropriate schedule of drug administration
1043567123 10435671 Leukocytosis
1043567123 10435671 Libido decreased
1043567123 10435671 Melanocytic naevus
1043567123 10435671 Myalgia
1043567123 10435671 Nausea
1043567123 10435671 Nervousness
1043567123 10435671 Pain
1043567123 10435671 Pruritus
1043567123 10435671 Pyrexia
1043567123 10435671 Rash
1043567123 10435671 Skin disorder
1043567123 10435671 Tooth infection
1043567123 10435671 Toothache

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
1043567123 10435671 1 20140817 0
1043567123 10435671 2 20140821 0
1043567123 10435671 3 201608 0