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
102323212 10232321 2 F 20160808 20140612 20160812 EXP FR-ROCHE-1416214 ROCHE . HIGHLIGHT ON DPYD GENE POLYMORPHISMS AND TREATMENT BY CAPECITABINE. SCANDINAVIAN JOURNAL OF CLINICAL AND LABORATORY INVESTIGATION 2016 JUL 20;:1-4. 0.00 F Y 0.00000 20160812 OT FR FR

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
102323212 10232321 1 PS CAPECITABINE. CAPECITABINE 1 Oral 20896 BID

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
102323212 10232321 1 Breast cancer metastatic

Outcome of event

Event ID CASEID OUTC COD
102323212 10232321 OT
102323212 10232321 DE

Reactions reported

Event ID CASEID DRUG REC ACT PT
102323212 10232321 Death
102323212 10232321 Diarrhoea
102323212 10232321 Gastrointestinal toxicity
102323212 10232321 Haematotoxicity
102323212 10232321 Neurotoxicity
102323212 10232321 Palmar-plantar erythrodysaesthesia syndrome
102323212 10232321 Vomiting

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

no results found

Therapies reported

no results found