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
91697002 9169700 2 F 20130228 20130320 20130318 20130331 EXP US-BRISTOL-MYERS SQUIBB COMPANY-17472507 BRISTOL MYERS SQUIBB 56.00 YR F Y 71.60000 KG 20130331 CN 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
91697002 9169700 1 PS CETUXIMAB 1 UNKNOWN TOTAL DOSE THIS COURSE WAS 865 MG D 0
91697002 9169700 2 SS RAMUCIRUMAB 1 TOTAL DOSE THIS COURSE WAS 498MG D 0
91697002 9169700 3 SS IRINOTECAN HCL 1 TOTAL DOSE THIS COURSE WAS 311 MG D 0
91697002 9169700 4 SS MORPHINE SULFATE 1 D 0
91697002 9169700 5 C ENOXAPARIN 1 D 0
91697002 9169700 6 C LEVOTHYROXINE 1 D 0
91697002 9169700 7 C ONDANSETRON 1 D 0
91697002 9169700 8 C SPIRONOLACTONE 1 D 0
91697002 9169700 9 C COMPAZINE 1 D 0
91697002 9169700 10 C GABAPENTIN 1 D 0
91697002 9169700 11 C LASIX 1 D 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
91697002 9169700 1 Colon cancer
91697002 9169700 2 Colorectal cancer
91697002 9169700 3 Colorectal cancer

Outcome of event

Event ID CASEID OUTC COD
91697002 9169700 HO

Reactions reported

Event ID CASEID DRUG REC ACT PT
91697002 9169700 Abdominal pain
91697002 9169700 Anaemia
91697002 9169700 Flank pain
91697002 9169700 Urostomy complication

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
91697002 9169700 1 20120303 0
91697002 9169700 2 20120303 0
91697002 9169700 3 20120503 0