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
900241423 9002414 23 F 20140912 20160915 20130107 20160923 EXP PHHY2009CA51459 SANDOZ 67.76 YR M Y 0.00000 20160923 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
900241423 9002414 1 SS GLEEVEC IMATINIB MESYLATE 1 Oral 400 MG, BID 0 400 MG TABLET BID
900241423 9002414 2 PS HYDROCHLOROTHIAZIDE. HYDROCHLOROTHIAZIDE 1 Unknown UNK Y 84912
900241423 9002414 3 C AMLODIPINE AMLODIPINE BESYLATE 1 Unknown 10 MG, UNK U 0 10 MG
900241423 9002414 4 C NORVASC AMLODIPINE BESYLATE 1 Unknown UNK 0
900241423 9002414 5 C WATER PILLS UNSPECIFIED INGREDIENT 1 Unknown U 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
900241423 9002414 1 Chronic myeloid leukaemia
900241423 9002414 2 Product used for unknown indication
900241423 9002414 3 Product used for unknown indication
900241423 9002414 4 Product used for unknown indication
900241423 9002414 5 Product used for unknown indication

Outcome of event

Event ID CASEID OUTC COD
900241423 9002414 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
900241423 9002414 Abdominal discomfort
900241423 9002414 Abscess limb
900241423 9002414 Alopecia
900241423 9002414 Arthralgia
900241423 9002414 Arthritis
900241423 9002414 Blood creatinine increased
900241423 9002414 Blood lactate dehydrogenase increased
900241423 9002414 Blood potassium decreased
900241423 9002414 Blood pressure decreased
900241423 9002414 Bone marrow failure
900241423 9002414 Bone pain
900241423 9002414 Bowel movement irregularity
900241423 9002414 Chest pain
900241423 9002414 Diarrhoea
900241423 9002414 Drug ineffective
900241423 9002414 Dyspepsia
900241423 9002414 Dysphonia
900241423 9002414 Dyspnoea
900241423 9002414 Erythema
900241423 9002414 Eye haemorrhage
900241423 9002414 Eye oedema
900241423 9002414 Eye pain
900241423 9002414 Eye swelling
900241423 9002414 Fall
900241423 9002414 Fatigue
900241423 9002414 Fluid retention
900241423 9002414 Hyperhidrosis
900241423 9002414 Incision site swelling
900241423 9002414 Joint swelling
900241423 9002414 Limb injury
900241423 9002414 Localised infection
900241423 9002414 Lymphocyte count decreased
900241423 9002414 Malaise
900241423 9002414 Mean cell volume increased
900241423 9002414 Muscle spasms
900241423 9002414 Musculoskeletal stiffness
900241423 9002414 Myalgia
900241423 9002414 Nasopharyngitis
900241423 9002414 Nausea
900241423 9002414 Night sweats
900241423 9002414 Oedema
900241423 9002414 Pain in extremity
900241423 9002414 Peripheral swelling
900241423 9002414 Prostatomegaly
900241423 9002414 Pyrexia
900241423 9002414 Rash
900241423 9002414 Red blood cell count decreased
900241423 9002414 Renal impairment
900241423 9002414 Skin exfoliation
900241423 9002414 Sunburn
900241423 9002414 Swelling
900241423 9002414 Testicular disorder
900241423 9002414 Urticaria
900241423 9002414 Weight decreased
900241423 9002414 Weight increased
900241423 9002414 Wound complication

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
900241423 9002414 1 20090901 0