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
126208851 12620885 1 I 20160725 20160804 20160804 EXP AU-DRREDDYS-USA/AUS/16/0081842 DR REDDYS POLASEK T, PERERA V, LUCIRE Y. SERIOUS ADVERSE DRUG REACTIONS TO ZOLPIDEM: DOES IMPAIRED METABOLIC CLEARANCE AND CONCURRENT SSRI/SNRI USE INCREASE RISK?. J PHARM PRACT RES. 2016;46(2):139-42. 46.00 YR M Y 0.00000 20160804 MD COUNTRY NOT SPECIFIED 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
126208851 12620885 1 PS SERTRALINE SERTRALINE HYDROCHLORIDE 1 Unknown U U UNKNOWN 76442
126208851 12620885 2 I ZOLPIDEM ZOLPIDEMOLPIDEM TARTRATE 1 Unknown UNKNOWN 0
126208851 12620885 3 C esomeprazole ESOMEPRAZOLE 1 Unknown UNKNOWN 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
126208851 12620885 1 Product used for unknown indication
126208851 12620885 2 Product used for unknown indication
126208851 12620885 3 Product used for unknown indication

Outcome of event

Event ID CASEID OUTC COD
126208851 12620885 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
126208851 12620885 Akathisia
126208851 12620885 Amnesia
126208851 12620885 Drug interaction
126208851 12620885 Fear
126208851 12620885 Homicidal ideation
126208851 12620885 Insomnia
126208851 12620885 Paranoia
126208851 12620885 Suicidal ideation

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

no results found

Therapies reported

no results found