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
126084201 12608420 1 I 20160719 20160729 20160729 EXP GB-MHRA-ROCHE-1793825 GB-FRESENIUS KABI-FK201604841 FRESENIUS KABI 61.00 YR M Y 0.00000 20160729 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
126084201 12608420 1 PS ONDANSETRON (MANUFACTURER UNKNOWN) ONDANSETRON 1 Unknown U U 76972 UNKNOWN
126084201 12608420 2 SS CAPECITABINE (Manufacturer unknown) CAPECITABINE 1 Unknown U U UNK 0 UNKNOWN
126084201 12608420 3 SS AVASTIN BEVACIZUMAB 1 Unknown 0
126084201 12608420 4 SS CYCLIZINE CYCLIZINE 1 Unknown 0
126084201 12608420 5 SS METOCLOPRAMIDE. METOCLOPRAMIDE 1 Unknown 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
126084201 12608420 1 Product used for unknown indication
126084201 12608420 2 Product used for unknown indication
126084201 12608420 3 Product used for unknown indication
126084201 12608420 4 Product used for unknown indication
126084201 12608420 5 Product used for unknown indication

Outcome of event

Event ID CASEID OUTC COD
126084201 12608420 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
126084201 12608420 Blood urine present
126084201 12608420 Change of bowel habit
126084201 12608420 Fatigue
126084201 12608420 Intestinal haemorrhage
126084201 12608420 Neuropathy peripheral
126084201 12608420 Protein urine

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

no results found

Therapies reported

no results found