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
126099801 12609980 1 I 20160719 20160801 20160801 EXP GB-AUROBINDO-AUR-APL-2016-09656 AUROBINDO 61.00 YR M Y 0.00000 20160801 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
126099801 12609980 1 PS Ondansetron ONDANSETRON 1 Unknown U U 78539
126099801 12609980 2 SS AVASTIN BEVACIZUMAB 1 Unknown U U 0
126099801 12609980 3 SS CYCLIZINE CYCLIZINE 1 Unknown U U 0
126099801 12609980 4 SS CAPECITABINE. CAPECITABINE 1 Unknown U U 0 TABLET
126099801 12609980 5 SS METOCLOPRAMIDE. METOCLOPRAMIDE 1 Unknown U U 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
126099801 12609980 1 Product used for unknown indication
126099801 12609980 2 Product used for unknown indication
126099801 12609980 3 Product used for unknown indication
126099801 12609980 4 Product used for unknown indication
126099801 12609980 5 Product used for unknown indication

Outcome of event

Event ID CASEID OUTC COD
126099801 12609980 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
126099801 12609980 Blood urine present
126099801 12609980 Change of bowel habit
126099801 12609980 Fatigue
126099801 12609980 Intestinal haemorrhage
126099801 12609980 Neuropathy peripheral
126099801 12609980 Protein urine

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

no results found

Therapies reported

no results found