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
127337843 12733784 3 F 20160722 20160920 20160912 20160927 EXP JP-ROCHE-1828256 ROCHE 67.55 YR F Y 48.00000 KG 20160928 MD JP JP

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
127337843 12733784 1 PS XELODA CAPECITABINE 1 Oral 2 WEEKS ADMINISTRATION FOLLOWED BY 1 WEEK REST Y 20896 1500 MG TABLET BID
127337843 12733784 2 SS TYKERB LAPATINIB DITOSYLATE 1 Oral DOSAGE IS UNCERTAIN. Y 0 1250 MG TABLET QD
127337843 12733784 3 C FERROUS SULFATE. FERROUS SULFATE 1 Oral 0 105 MG TABLET BID

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
127337843 12733784 1 Breast cancer
127337843 12733784 2 Breast cancer
127337843 12733784 3 Anaemia

Outcome of event

Event ID CASEID OUTC COD
127337843 12733784 HO

Reactions reported

Event ID CASEID DRUG REC ACT PT
127337843 12733784 Acute kidney injury
127337843 12733784 Diarrhoea

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
127337843 12733784 1 20160721 20160806 0
127337843 12733784 2 20160721 20160806 0
127337843 12733784 3 20160127 20160806 0