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
125997041 12599704 1 I 20160303 20160727 20160727 PER US-SA-2016SA045804 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
125997041 12599704 1 PS AMBIEN ZOLPIDEM TARTRATE 1 Oral 10MG IN JANUARY U UNKNOWN 19908 10 MG FILM-COATED TABLET
125997041 12599704 2 SS AMBIEN ZOLPIDEM TARTRATE 1 Oral 5MG IN FEBRUARY U UNKNOWN 19908 5 MG FILM-COATED TABLET

Indications of drugs used

no results found

Outcome of event

Event ID CASEID OUTC COD
125997041 12599704 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
125997041 12599704 Chills
125997041 12599704 Crying
125997041 12599704 Depressed mood
125997041 12599704 Drug withdrawal syndrome
125997041 12599704 Hyperhidrosis
125997041 12599704 Insomnia
125997041 12599704 Muscle spasms
125997041 12599704 Suicidal ideation

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
125997041 12599704 1 201601 0
125997041 12599704 2 201602 0