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
953984914 9539849 14 F 20160908 20130920 20160915 EXP PHHY2013CA104168 NOVARTIS 0.00 F Y 0.00000 20160915 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
953984914 9539849 1 PS TASIGNA NILOTINIB 1 Oral 300 MG, BID 22068 300 MG CAPSULE BID
953984914 9539849 2 SS TASIGNA NILOTINIB 1 Oral 300 MG BID ONE DAY AND 150 MG BID THE NEXT DAY 22068 CAPSULE
953984914 9539849 3 SS TASIGNA NILOTINIB 1 Oral 300 MG, BID 22068 300 MG CAPSULE BID
953984914 9539849 4 SS LASIX FUROSEMIDE 1 Unknown U 0
953984914 9539849 5 SS WELLBUTRIN BUPROPION HYDROCHLORIDE 1 Unknown Y 0
953984914 9539849 6 C MS CONTIN MORPHINE SULFATE 1 Unknown U 0
953984914 9539849 7 C FENTANYL. FENTANYL 1 Unknown U 0
953984914 9539849 8 C DEPO-PROVERA MEDROXYPROGESTERONE ACETATE 1 Unknown U 0 INJECTION

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
953984914 9539849 1 Chronic myeloid leukaemia
953984914 9539849 4 Product used for unknown indication
953984914 9539849 5 Product used for unknown indication
953984914 9539849 6 Pain
953984914 9539849 7 Arthralgia
953984914 9539849 8 Product used for unknown indication

Outcome of event

Event ID CASEID OUTC COD
953984914 9539849 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
953984914 9539849 Abdominal distension
953984914 9539849 Abdominal pain
953984914 9539849 Arrhythmia
953984914 9539849 Arthralgia
953984914 9539849 Asthenia
953984914 9539849 Balance disorder
953984914 9539849 Blister
953984914 9539849 Blood pressure fluctuation
953984914 9539849 Blood test abnormal
953984914 9539849 Decreased appetite
953984914 9539849 Depressed level of consciousness
953984914 9539849 Diabetes mellitus
953984914 9539849 Dizziness
953984914 9539849 Dry skin
953984914 9539849 Dyspnoea
953984914 9539849 Fatigue
953984914 9539849 Fluid retention
953984914 9539849 Gastrooesophageal reflux disease
953984914 9539849 Generalised oedema
953984914 9539849 Headache
953984914 9539849 Hunger
953984914 9539849 Hyperhidrosis
953984914 9539849 Hypoaesthesia
953984914 9539849 Laceration
953984914 9539849 Lactose intolerance
953984914 9539849 Lethargy
953984914 9539849 Loss of consciousness
953984914 9539849 Lung disorder
953984914 9539849 Migraine
953984914 9539849 Mouth swelling
953984914 9539849 Movement disorder
953984914 9539849 Nasal oedema
953984914 9539849 Oral mucosal blistering
953984914 9539849 Pain
953984914 9539849 Palpitations
953984914 9539849 Parosmia
953984914 9539849 Photophobia
953984914 9539849 Pollakiuria
953984914 9539849 Pruritus
953984914 9539849 Skin atrophy
953984914 9539849 Skin irritation
953984914 9539849 Skin sensitisation
953984914 9539849 Somnolence
953984914 9539849 Tunnel vision
953984914 9539849 Vaginal odour
953984914 9539849 Visual impairment
953984914 9539849 Vomiting
953984914 9539849 Weight increased
953984914 9539849 Wound
953984914 9539849 Wound haemorrhage

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
953984914 9539849 1 20130208 0