The Safety Rates Drug Report

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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
125696541 12569654 1 I 20160713 20160719 20160719 PER PHEH2016US017684 NOVARTIS 0.00 M Y 0.00000 20160719 MD US US

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
125696541 12569654 1 PS GLEEVEC IMATINIB MESYLATE 1 Unknown 400 MG, UNK 21588 400 MG
125696541 12569654 2 SS GLEEVEC IMATINIB MESYLATE 1 Unknown 200 MG, UNK 21588 200 MG
125696541 12569654 3 SS GLEEVEC IMATINIB MESYLATE 1 Unknown 100 MG, QD F0023 21588 100 MG QD
125696541 12569654 4 C PEPCID FAMOTIDINE 1 Unknown UNK, BID U UNKNOWN 0 BID
125696541 12569654 5 C Calcium CALCIUM 1 Unknown U UNKNOWN 0
125696541 12569654 6 C ZETIA EZETIMIBE 1 Unknown U UNKNOWN 0
125696541 12569654 7 C TURMERIC TURMERIC 1 Unknown U UNKNOWN 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
125696541 12569654 1 Chronic myeloid leukaemia
125696541 12569654 4 Gastrooesophageal reflux disease
125696541 12569654 5 Product used for unknown indication
125696541 12569654 6 Blood cholesterol increased

Outcome of event

Event ID CASEID OUTC COD
125696541 12569654 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
125696541 12569654 Haemoglobin decreased
125696541 12569654 Polyp
125696541 12569654 Renal failure

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
125696541 12569654 1 200810 0