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
125990991 12599099 1 I 20101227 20101229 20160727 20160727 PER US-SANOFI-AVENTIS-2010SA078556 AVENTIS 76.00 YR E F Y 0.00000 20160727 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
125990991 12599099 1 PS ZOLPIDEM TARTRATE EXTENDED RELEASE ZOLPIDEM TARTRATE 1 Oral UNKNOWN 21774 12.5 MG MODIFIED-RELEASE TABLET QD
125990991 12599099 2 SS ZOLPIDEM TARTRATE EXTENDED RELEASE ZOLPIDEM TARTRATE 1 Oral UNKNOWN 21774 12.5 MG MODIFIED-RELEASE TABLET QD

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
125990991 12599099 1 Sleep disorder
125990991 12599099 2 Sleep disorder

Outcome of event

no results found

Reactions reported

Event ID CASEID DRUG REC ACT PT
125990991 12599099 Diarrhoea
125990991 12599099 Drug ineffective
125990991 12599099 Gastrointestinal disorder
125990991 12599099 Insomnia
125990991 12599099 Pain
125990991 12599099 Sleep disorder

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
125990991 12599099 1 20101222 0
125990991 12599099 2 20110417 0