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
5229711 6231103 I 5229711-5 20070111 20070122 20070206 EXP JP-ELI_LILLY_AND_COMPANY-JP200701004526 ELI LILLY AND COMPANY 65 YR M Y 47 KG 20070205 MD JAPAN

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
5229711 1008117660 PS DULOXETINE HYDROCHLORIDE 2 21427
5229711 1008117661 SS DULOXETINE HYDROCHLORIDE 2 021427
5229711 1008117662 C HALCION 1 ORAL 0.5 MG, DAILY (1/D)

Indications of drugs used

Event ID DRUG SEQ INDI PT
5229711 1008117660 MAJOR DEPRESSION
5229711 1008117662 INSOMNIA

Outcome of event

Event ID OUTC COD
5229711 HO

Reactions reported

Event ID PT
5229711 ALANINE AMINOTRANSFERASE INCREASED
5229711 ASPARTATE AMINOTRANSFERASE INCREASED
5229711 BLOOD LACTATE DEHYDROGENASE INCREASED
5229711 BLOOD TRIGLYCERIDES INCREASED
5229711 CONVULSION
5229711 DECREASED APPETITE
5229711 GAMMA-GLUTAMYLTRANSFERASE INCREASED
5229711 HEPATIC FUNCTION ABNORMAL
5229711 IRRITABILITY
5229711 LIVER DISORDER
5229711 NAUSEA
5229711 THIRST

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
5229711 1008117660 20061228 20070104 8 DAY
5229711 1008117661 20070105 20070108 4 DAY
5229711 1008117662 20061221