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
125561711 12556171 1 I 20160705 20160714 20160714 EXP AU-PURDUE-USA-2016-0132071 PURDUE PLASEK, THOMAS M., ET. AL. SERIOUS ADVERSE DRUG REACTIONS TO ZOLPIDEM: DOES IMPAIRED METABOLIC CLEARANCE AND CONCURRENT SSRI/SNRI USE INCREASE RISK?. JOURNAL OF PHARMACY PRACTICE AND RESEARCH. 2016;46:139-142 46.00 YR M Y 0.00000 20160714 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
125561711 12556171 1 PS ZOLPIDEM TARTRATE. ZOLPIDEM TARTRATE 1 Oral U U UNKNOWN 22328
125561711 12556171 2 SS SERTRALINE SERTRALINE HYDROCHLORIDE 1 Oral U U UNKNOWN 0
125561711 12556171 3 SS ESOMEPRAZOLE ESOMEPRAZOLE 1 Oral U U UNKNOWN 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
125561711 12556171 1 Insomnia
125561711 12556171 2 Product used for unknown indication
125561711 12556171 3 Product used for unknown indication

Outcome of event

Event ID CASEID OUTC COD
125561711 12556171 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
125561711 12556171 Akathisia
125561711 12556171 Amnesia
125561711 12556171 Fear
125561711 12556171 Homicidal ideation
125561711 12556171 Insomnia
125561711 12556171 Paranoia
125561711 12556171 Suicidal ideation

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

no results found

Therapies reported

no results found