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
5205323 6124767 F 4 5205323-4 20060718 20061215 20070108 EXP 228937 GENENTECH, INC. 49 YR F N 83 KG 20070105 MD UNITED KINGDOM

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
5205323 1008030461 PS AVASTIN 1 INTRAVENOUS 415 MG, INTRAVNEOUS Y D
5205323 1008062442 C IRINOTECAN HCL 1
5205323 1008062443 C FOLINIC ACID (LECOVORIN CALCIUM) 2
5205323 1008062444 C FLUOROURACIL 1

Indications of drugs used

Event ID DRUG SEQ INDI PT
5205323 1008030461 DRUG USE FOR UNKNOWN INDICATION

Outcome of event

Event ID OUTC COD
5205323 OT

Reactions reported

Event ID PT
5205323 ALANINE AMINOTRANSFERASE INCREASED
5205323 BLOOD ALKALINE PHOSPHATASE INCREASED
5205323 BLOOD BILIRUBIN INCREASED
5205323 GAMMA-GLUTAMYLTRANSFERASE INCREASED
5205323 JAUNDICE
5205323 NEUTROPENIA

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

Event ID RPSR COD
5205323 FGN
5205323 HP
5205323 OTH

Therapies reported

Event ID DRUG SEQ START DT END DT DUR DUR COD
5205323 1008030461 20060502 20060718