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
126475061 12647506 1 I 20160712 0 20160811 20160811 DIR 57.78 YR M N 77.60000 KG 20160808 N MD US

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
126475061 12647506 1 PS 5-FLUOROURACIL (5-FU) FLUOROURACIL 1 0 57106 MG
126475061 12647506 2 SS LEUCOVORIN CALCIUM. LEUCOVORIN CALCIUM 1 0 6304 MG
126475061 12647506 3 SS ELOXATIN OXALIPLATIN 1 0 1122.2 MG

Indications of drugs used

no results found

Outcome of event

Event ID CASEID OUTC COD
126475061 12647506 HO

Reactions reported

Event ID CASEID DRUG REC ACT PT
126475061 12647506 Abdominal pain
126475061 12647506 Bile duct stone
126475061 12647506 Chest pain
126475061 12647506 Haemangioma of liver
126475061 12647506 Hepatic steatosis
126475061 12647506 Liver function test increased
126475061 12647506 Pancreatitis

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

Event ID CASEID RPSR COD
126475061 12647506 HP

Therapies reported

Event ID CASEID DSG DRUG SEQ START DT END DT DUR DUR COD
126475061 12647506 1 20151116 0
126475061 12647506 2 20160705 0
126475061 12647506 3 20160613 0