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
946364016 9463640 16 F 20131208 20160711 20130819 20160714 EXP PHHY2013CA088764 NOVARTIS 64.22 YR M Y 0.00000 20160714 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
946364016 9463640 1 PS GLEEVEC IMATINIB MESYLATE 1 Oral 400 MG, QD 21588 400 MG QD
946364016 9463640 2 SS GLEEVEC IMATINIB MESYLATE 1 Oral 400 MG, QD 21588 400 MG QD
946364016 9463640 3 SS GLEEVEC IMATINIB MESYLATE 1 Oral 400 MG, QD 21588 400 MG QD
946364016 9463640 4 SS GLEEVEC IMATINIB MESYLATE 1 Unknown 300 MG, QD 21588 300 MG QD
946364016 9463640 5 SS GLEEVEC IMATINIB MESYLATE 1 Oral 200 MG, QD 21588 200 MG QD
946364016 9463640 6 SS IMATINIB IMATINIB 1 Unknown UNK 21588
946364016 9463640 7 C FERROUS FUMARATE FERROUS FUMARATE 1 Oral 300 MG, QD 0 300 MG QD
946364016 9463640 8 C FUROSEMIDE. FUROSEMIDE 1 Oral 40 MG, BID 0 40 MG BID
946364016 9463640 9 C SPIRONOLACTONE. SPIRONOLACTONE 1 Unknown 25 MG, QD 0 25 MG QD
946364016 9463640 10 C NOVOLIN INSULIN HUMAN 1 Unknown 15 U, QD 0 15 DF QD
946364016 9463640 11 C INSULIN INSULIN NOS 1 Unknown 30 U, QAM 0 30 DF
946364016 9463640 12 C RABEPRAZOLE RABEPRAZOLE 1 Unknown UNK 0
946364016 9463640 13 C PANTOLOC//PANTOPRAZOLE SODIUM SESQUIHYDRATE PANTOPRAZOLE SODIUM 1 Unknown UNK 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
946364016 9463640 1 Chronic myeloid leukaemia
946364016 9463640 6 Product used for unknown indication
946364016 9463640 7 Product used for unknown indication
946364016 9463640 8 Product used for unknown indication
946364016 9463640 9 Product used for unknown indication
946364016 9463640 10 Product used for unknown indication
946364016 9463640 11 Diabetes mellitus
946364016 9463640 12 Product used for unknown indication
946364016 9463640 13 Product used for unknown indication

Outcome of event

Event ID CASEID OUTC COD
946364016 9463640 OT
946364016 9463640 HO
946364016 9463640 DE

Reactions reported

Event ID CASEID DRUG REC ACT PT
946364016 9463640 Abdominal discomfort
946364016 9463640 Abdominal pain upper
946364016 9463640 Anaemia
946364016 9463640 Arthritis infective
946364016 9463640 Blood creatinine increased
946364016 9463640 Blood iron decreased
946364016 9463640 Blood urea increased
946364016 9463640 Chills
946364016 9463640 Death
946364016 9463640 Decreased appetite
946364016 9463640 Device related infection
946364016 9463640 Diarrhoea
946364016 9463640 Dysgeusia
946364016 9463640 Escherichia infection
946364016 9463640 Faeces discoloured
946364016 9463640 Fatigue
946364016 9463640 Fluid retention
946364016 9463640 Gastrointestinal haemorrhage
946364016 9463640 Haematochezia
946364016 9463640 Haemoglobin decreased
946364016 9463640 Headache
946364016 9463640 Heart rate increased
946364016 9463640 Hepatic cirrhosis
946364016 9463640 Hepatic failure
946364016 9463640 Infection
946364016 9463640 Lung infection
946364016 9463640 Nausea
946364016 9463640 Peripheral swelling
946364016 9463640 Pyrexia
946364016 9463640 Red blood cell count decreased
946364016 9463640 Renal disorder
946364016 9463640 Renal failure
946364016 9463640 Serum ferritin increased
946364016 9463640 Swelling
946364016 9463640 Underdose
946364016 9463640 Varicose vein
946364016 9463640 White blood cell count 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
946364016 9463640 1 20070801 201306 0
946364016 9463640 2 201308 20131208 0
946364016 9463640 3 20140314 0
946364016 9463640 4 201507 0
946364016 9463640 6 201306 0