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
126581091 12658109 1 I 20160812 20160817 20160817 EXP BR-ROCHE-1813884 ROCHE 0.00 F Y 49.00000 KG 20160817 PH BR BR

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
126581091 12658109 1 PS XELODA CAPECITABINE 1 Unknown 3 TABLETS DAILY DURING 14 DAYS EVERY 21 DAYS U X3786B16,X3819B01 20896 150 MG TABLET
126581091 12658109 2 SS XELODA CAPECITABINE 1 Unknown 3 TABLETS DAILY DURING 14 DAYS EVERY 21 DAYS U X3786B16,X3819B01 20896 500 MG TABLET
126581091 12658109 3 SS TEVAOXALI OXALIPLATIN 1 Intravenous (not otherwise specified) U 14L15MJ 0 189.41 MG
126581091 12658109 4 C VENLAFAXINE VENLAFAXINE HYDROCHLORIDE 1 Unknown 0 70 MG
126581091 12658109 5 C ALLEGRA FEXOFENADINE HYDROCHLORIDE 1 Unknown 0 120 MG

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
126581091 12658109 1 Small intestine carcinoma
126581091 12658109 3 Small intestine carcinoma

Outcome of event

Event ID CASEID OUTC COD
126581091 12658109 HO

Reactions reported

Event ID CASEID DRUG REC ACT PT
126581091 12658109 Colitis
126581091 12658109 Dehydration
126581091 12658109 Hypokalaemia

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
126581091 12658109 1 20160525 0
126581091 12658109 2 20160525 0
126581091 12658109 3 20160525 0