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
112397595 11239759 5 F 20160823 20150706 20160901 EXP PHHY2015CA080905 NOVARTIS 0.00 F Y 0.00000 20160902 CN COUNTRY NOT SPECIFIED CA

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
112397595 11239759 1 PS TASIGNA NILOTINIB 1 Oral 300 MG, BID 22068 300 MG CAPSULE BID

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
112397595 11239759 1 Chronic myeloid leukaemia

Outcome of event

no results found

Reactions reported

Event ID CASEID DRUG REC ACT PT
112397595 11239759 Acne
112397595 11239759 Alopecia
112397595 11239759 Anxiety
112397595 11239759 Asthenia
112397595 11239759 Chest discomfort
112397595 11239759 Constipation
112397595 11239759 Diabetes mellitus
112397595 11239759 Discomfort
112397595 11239759 Dry skin
112397595 11239759 Dyspepsia
112397595 11239759 Hyperchlorhydria
112397595 11239759 Impaired healing
112397595 11239759 Nasopharyngitis
112397595 11239759 Oropharyngeal pain
112397595 11239759 Pain
112397595 11239759 Pruritus
112397595 11239759 Rash papular
112397595 11239759 Secretion discharge
112397595 11239759 Skin disorder
112397595 11239759 Skin hypertrophy
112397595 11239759 Urinary tract infection
112397595 11239759 Uterine disorder
112397595 11239759 Vaginal discharge
112397595 11239759 Vaginal infection
112397595 11239759 Vaginal lesion
112397595 11239759 Vulvovaginal discomfort

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
112397595 11239759 1 20150512 0