The Safety Rates Drug Report

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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
125296051 12529605 1 I 20160628 20160706 20160706 EXP US-ASTRAZENECA-2016SE71172 ASTRAZENECA POLASEK T. SERIOUS ADVERSE DRUG REACTIONS TO ZOLPIDEM: DOES IMPAIRED METABOLIC CLEARANCE AND CONCURRENT SSRI/SNRI USE INCREASE RISK.. JOURNAL OF PHARMACY PRACTICE AND RESEARCH. 2016; 46((2)):139-142. 46.00 YR M Y 0.00000 20160706 MD AU AU

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
125296051 12529605 1 PS ESOMEPRAZOLE MAGNESIUM. ESOMEPRAZOLE MAGNESIUM 1 Oral UNK U 21153
125296051 12529605 2 I SERTRALINE HCL SERTRALINE HYDROCHLORIDE 1 Unknown UNK U 0
125296051 12529605 3 I ZOLPIDEM ZOLPIDEMOLPIDEM TARTRATE 1 Unknown UNK U U 0
125296051 12529605 4 I ZOLPIDEM ZOLPIDEMOLPIDEM TARTRATE 1 Unknown UNK U U 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
125296051 12529605 3 Insomnia
125296051 12529605 4 Stress

Outcome of event

Event ID CASEID OUTC COD
125296051 12529605 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
125296051 12529605 Akathisia
125296051 12529605 Amnesia
125296051 12529605 Drug interaction
125296051 12529605 Fear
125296051 12529605 Homicidal ideation
125296051 12529605 Insomnia
125296051 12529605 Paranoia
125296051 12529605 Suicidal ideation

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

no results found

Therapies reported

no results found