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
127794541 12779454 1 I 20120210 20120627 20160926 20160926 EXP PHHY2012IQ055376 NOVARTIS 34.03 YR F Y 0.00000 20160926 CN COUNTRY NOT SPECIFIED IQ

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
127794541 12779454 1 SS GLIVEC IMATINIB MESYLATE 1 Oral 400 MG, QD Y 0 400 MG CAPSULE QD
127794541 12779454 2 SS GLIVEC IMATINIB MESYLATE 1 Oral 600 MG, QD Y 0 600 MG CAPSULE QD
127794541 12779454 3 SS GLIVEC IMATINIB MESYLATE 1 Oral 400 MG, QD Y 0 400 MG CAPSULE QD
127794541 12779454 4 SS GLIVEC IMATINIB MESYLATE 1 Oral 600 MG, QD Y 0 600 MG CAPSULE QD
127794541 12779454 5 SS GLIVEC IMATINIB MESYLATE 1 Oral 400 MG, QD Y 0 400 MG CAPSULE QD
127794541 12779454 6 PS TASIGNA NILOTINIB 1 Unknown U 22068 CAPSULE
127794541 12779454 7 C METFORMINE METFORMIN HYDROCHLORIDE 1 Oral 1 DF, BID U 0 1 DF BID
127794541 12779454 8 C DOSTINEX CABERGOLINE 1 Oral 0.5 DF, PER 03 DAYS U 0 .5 DF
127794541 12779454 9 C GLUCOBAY ACARBOSE 1 Oral 1 DF, Q12H U 0 1 DF TABLET Q12H
127794541 12779454 10 C SUPRAX//CEFIXIME 2 Unknown 400 MG, QD U 0 400 MG QD
127794541 12779454 11 C PARACETAMOL ACETAMINOPHEN 1 Oral UNK (SOS) U 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
127794541 12779454 1 Chronic myeloid leukaemia
127794541 12779454 6 Product used for unknown indication
127794541 12779454 7 Product used for unknown indication
127794541 12779454 8 Product used for unknown indication
127794541 12779454 9 Product used for unknown indication
127794541 12779454 10 Product used for unknown indication
127794541 12779454 11 Product used for unknown indication

Outcome of event

no results found

Reactions reported

Event ID CASEID DRUG REC ACT PT
127794541 12779454 Abdominal pain upper
127794541 12779454 Arthralgia
127794541 12779454 Asthenia
127794541 12779454 Blood creatinine increased
127794541 12779454 Blood uric acid increased
127794541 12779454 Bone pain
127794541 12779454 Cough
127794541 12779454 Diarrhoea
127794541 12779454 Dizziness
127794541 12779454 Dysgeusia
127794541 12779454 Dysmenorrhoea
127794541 12779454 Fatigue
127794541 12779454 Flushing
127794541 12779454 Headache
127794541 12779454 Hyperglycaemia
127794541 12779454 Hypertension
127794541 12779454 Influenza
127794541 12779454 Leukopenia
127794541 12779454 Menstrual disorder
127794541 12779454 Myalgia
127794541 12779454 Nausea
127794541 12779454 Neck pain
127794541 12779454 Oedema
127794541 12779454 Oedema peripheral
127794541 12779454 Ovarian cyst
127794541 12779454 Peripheral coldness
127794541 12779454 Pyrexia
127794541 12779454 Renal pain
127794541 12779454 Skin discolouration
127794541 12779454 Swelling
127794541 12779454 Syncope
127794541 12779454 Thrombocytosis
127794541 12779454 Tonsillitis
127794541 12779454 Tumour marker increased
127794541 12779454 Weight increased

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
127794541 12779454 1 20100120 201507 0
127794541 12779454 2 201507 201510 0
127794541 12779454 3 201510 201512 0
127794541 12779454 4 20151211 20151228 0
127794541 12779454 5 20151228 201603 0
127794541 12779454 7 201303 0
127794541 12779454 8 201303 0
127794541 12779454 9 201406 0
127794541 12779454 10 20141211 0