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
127415041 12741504 1 I 20061031 0 20160913 20160913 DIR FDA-CTU 51.92 YR M N 130.00000 KG 20160912 N MD US 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
127415041 12741504 1 PS 5-FLUOROURACIL (5-FU) FLUOROURACIL 1 D D 0 29680 MG
127415041 12741504 2 SS BEVACIZUMAB (RHUMAB VEGF) BEVACIZUMAB 1 0 2636 MG
127415041 12741504 3 SS LEUCOVORIN CALCIUM. LEUCOVORIN CALCIUM 1 0 4240 MG
127415041 12741504 4 SS ELOXATIN OXALIPLATIN 1 0 900 MG

Indications of drugs used

no results found

Outcome of event

Event ID CASEID OUTC COD
127415041 12741504 HO

Reactions reported

Event ID CASEID DRUG REC ACT PT
127415041 12741504 Back pain
127415041 12741504 Chills
127415041 12741504 Device related infection
127415041 12741504 Hyperhidrosis
127415041 12741504 Muscle spasms
127415041 12741504 Purulent discharge
127415041 12741504 Pyrexia
127415041 12741504 Staphylococcus test positive

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

Event ID CASEID RPSR COD
127415041 12741504 HP

Therapies reported

Event ID CASEID DSG DRUG SEQ START DT END DT DUR DUR COD
127415041 12741504 1 20061010 0
127415041 12741504 2 20061010 0
127415041 12741504 3 20061010 0
127415041 12741504 4 20061010 0