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
125874751 12587475 1 I 20160719 20160725 20160725 EXP PHFR2016GB005921 NOVARTIS 61.00 YR M Y 0.00000 20160725 OT GB GB

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
125874751 12587475 1 PS ONDANSETRON ONDANSETRON 1 Unknown U 20007
125874751 12587475 2 SS AVASTIN BEVACIZUMAB 1 Unknown U 0
125874751 12587475 3 SS CYCLIZINE CYCLIZINE 1 Unknown U 0
125874751 12587475 4 SS CAPECITABINE. CAPECITABINE 1 Unknown U 0
125874751 12587475 5 SS METOCLOPRAMIDE. METOCLOPRAMIDE 1 Unknown U 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
125874751 12587475 1 Product used for unknown indication
125874751 12587475 2 Product used for unknown indication
125874751 12587475 3 Product used for unknown indication
125874751 12587475 4 Product used for unknown indication
125874751 12587475 5 Product used for unknown indication

Outcome of event

Event ID CASEID OUTC COD
125874751 12587475 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
125874751 12587475 Blood urine present
125874751 12587475 Change of bowel habit
125874751 12587475 Fatigue
125874751 12587475 Intestinal haemorrhage
125874751 12587475 Neuropathy peripheral
125874751 12587475 Protein urine

Reporting Sources (this data is often not reported and may therefore be missing here)

no results found

Therapies reported

no results found