The Safety Rates Drug Report

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Drug     Injury     Quarter    

Person who experienced the adverse event (patient)

Event ID CASE I F COD FOLL SEQ IMAGE EVENT DT MFR DT FDA DT REPT COD MFR NUM MFR SNDR AGE AGE COD GNDR COD E SUB WT WT COD REPT DT OCCP COD DEATH DT TO MFR CONFID REPORTER COUNTRY
6382104 7038923 F 6382104-X 20090201 20090924 20090930 EXP FR-BRISTOL-MYERS SQUIBB COMPANY-14682983 BRISTOL-MYERS SQUIBB COMPANY 84 YR M Y 20090930 MD 20090408 GERMANY

Drug(s) used by person

Event ID DRUG SEQ ROLE COD DRUGNAME VAL VBM ROUTE DOSE VBM DECHAL RECHAL LOT NUM EXP DT NDA NUM
6382104 1012352978 PS ERBITUX 1 INTRAVENOUS
6382104 1012352979 SS FLUOROURACIL 1 INTRAVENOUS SOLUTION FOR INJECTION
6382104 1012352980 SS CAMPTOSAR 1 INTRAVENOUS SOLUTION FOR INJ
6382104 1012352981 C ICAZ 2
6382104 1012352982 C ALLOPURINOL 1
6382104 1012352983 C LIPANTHYL 2

Indications of drugs used

Event ID DRUG SEQ INDI PT
6382104 1012352978 COLORECTAL CANCER
6382104 1012352979 COLORECTAL CANCER
6382104 1012352980 COLORECTAL CANCER

Outcome of event

Event ID OUTC COD
6382104 DE
6382104 HO

Reactions reported

Event ID PT
6382104 ASTHENIA
6382104 DECREASED APPETITE
6382104 DIARRHOEA
6382104 MOUTH ULCERATION
6382104 MULTI-ORGAN FAILURE
6382104 NEUTROPENIA
6382104 STOMATITIS
6382104 VOMITING

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

no results found

Therapies reported

Event ID DRUG SEQ START DT END DT DUR DUR COD
6382104 1012352978 20090216 20090330 41 DAY
6382104 1012352979 20090216 20090330 41 DAY
6382104 1012352980 20090216 20090330 41 DAY