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
126494892 12649489 2 F 20160830 20160812 20160908 EXP JP-SA-2016SA146482 AVENTIS 0.00 A M Y 0.00000 20160908 PH JP JP

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
126494892 12649489 1 PS MYSLEE ZOLPIDEM TARTRATE 1 Oral 30MG-10MG, TWICE DAILY U UNKNOWN 19908 FILM-COATED TABLET BID
126494892 12649489 2 SS SEROQUEL QUETIAPINE FUMARATE 1 Unknown Y UNKNOWN 0
126494892 12649489 3 C LORAZEPAM. LORAZEPAM 1 Oral 0
126494892 12649489 4 C OLANZAPINE. OLANZAPINE 1 Unknown 0
126494892 12649489 5 C LEXAPRO ESCITALOPRAM OXALATE 1 Unknown 0
126494892 12649489 6 C ROZEREM RAMELTEON 1 Unknown 0
126494892 12649489 7 C BELSOMRA SUVOREXANT 1 Unknown 0
126494892 12649489 8 C ZOLPIDEM ZOLPIDEMOLPIDEM TARTRATE 1 Unknown 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
126494892 12649489 1 Analgesic therapy

Outcome of event

Event ID CASEID OUTC COD
126494892 12649489 HO
126494892 12649489 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
126494892 12649489 Delirium
126494892 12649489 Eating disorder
126494892 12649489 Intentional overdose
126494892 12649489 Off label use
126494892 12649489 Pneumonia aspiration
126494892 12649489 Withdrawal syndrome

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

no results found

Therapies reported

no results found