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
125997021 12599702 1 I 20160229 20160727 20160727 PER US-SA-2016SA042503 AVENTIS 0.00 A 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
125997021 12599702 1 PS AMBIEN ZOLPIDEM TARTRATE 1 Unknown U UNKNOWN 19908 TABLET
125997021 12599702 2 SS AMBIEN ZOLPIDEM TARTRATE 1 Unknown U UNKNOWN 19908 TABLET

Indications of drugs used

no results found

Outcome of event

no results found

Reactions reported

Event ID CASEID DRUG REC ACT PT
125997021 12599702 Drug ineffective
125997021 12599702 Hangover
125997021 12599702 Unevaluable event

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

no results found

Therapies reported

no results found