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
5794784 6277269 F 5794784-8 20070206 20080624 20080630 EXP A0644683A GLAXOSMITHKLINE 48 YR F Y 65 KG 20080630 MD UNITED STATES

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
5794784 1010109994 PS LAPATINIB 2 ORAL 1500MG PER DAY 22059
5794784 1010109995 C AUGMENTIN '125' 1 ORAL 875MG TWICE PER DAY

Indications of drugs used

Event ID DRUG SEQ INDI PT
5794784 1010109995 SKIN INFECTION

Outcome of event

Event ID OUTC COD
5794784 OT

Reactions reported

Event ID PT
5794784 HEPATIC ENZYME INCREASED
5794784 TRANSAMINASES INCREASED

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
5794784 1010109994 20060714 20070525 316 DAY
5794784 1010109995 20070108 20070117 10 DAY