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
677282210 6772822 10 F 200705 20160728 20080926 20160804 EXP PHHY2008CA22231 NOVARTIS 64.88 YR M Y 0.00000 20160804 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
677282210 6772822 1 PS GLEEVEC IMATINIB MESYLATE 1 Oral 400 MG, QD 21588 400 MG QD
677282210 6772822 2 SS GLEEVEC IMATINIB MESYLATE 1 Oral 400 MG, QD 21588 400 MG QD
677282210 6772822 3 C LIPITOR ATORVASTATIN CALCIUM 1 Unknown U 0
677282210 6772822 4 C VITAMIN B12 CYANOCOBALAMIN 1 Unknown Y 0
677282210 6772822 5 C CRESTOR ROSUVASTATIN CALCIUM 1 Unknown U 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
677282210 6772822 1 Acute lymphocytic leukaemia
677282210 6772822 3 Product used for unknown indication
677282210 6772822 4 Product used for unknown indication
677282210 6772822 5 Product used for unknown indication

Outcome of event

Event ID CASEID OUTC COD
677282210 6772822 DS
677282210 6772822 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
677282210 6772822 Abdominal discomfort
677282210 6772822 Anaemia
677282210 6772822 Blister
677282210 6772822 Decreased appetite
677282210 6772822 Dysgeusia
677282210 6772822 Dyskinesia
677282210 6772822 Hypoaesthesia
677282210 6772822 Hypophagia
677282210 6772822 Mobility decreased
677282210 6772822 Muscle spasms
677282210 6772822 Myalgia
677282210 6772822 Nausea
677282210 6772822 Pain in extremity
677282210 6772822 Paraesthesia
677282210 6772822 Sunburn
677282210 6772822 Tremor
677282210 6772822 Weight increased
677282210 6772822 Wrong technique in product usage process

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
677282210 6772822 1 200505 200810 0