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
126387981 12638798 1 I 20151123 20160801 20160809 20160809 EXP FR-AFSSAPS-TO20161581 FR-FRI-1000086763 FOREST 69.56 YR M Y 0.00000 20160809 OT DK FR

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
126387981 12638798 1 PS ESCITALOPRAM ESCITALOPRAM OXALATE 1 Oral 5 MG Y 21323 5 MG FILM-COATED TABLET QD
126387981 12638798 2 SS RISPERIDONE. RISPERIDONE 1 Oral Y 0 1 MG
126387981 12638798 3 SS RISPERIDONE. RISPERIDONE 1 Oral Y 0 5 MG
126387981 12638798 4 SS ALPRAZOLAM. ALPRAZOLAM 1 Oral Y 0 .25 MG
126387981 12638798 5 SS ALPRAZOLAM. ALPRAZOLAM 1 Oral Y 0 .5 MG

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
126387981 12638798 1 Major depression
126387981 12638798 2 Major depression
126387981 12638798 4 Major depression

Outcome of event

Event ID CASEID OUTC COD
126387981 12638798 HO

Reactions reported

Event ID CASEID DRUG REC ACT PT
126387981 12638798 Confusional state
126387981 12638798 Delusion
126387981 12638798 Hyponatraemia
126387981 12638798 Somnolence

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
126387981 12638798 1 201512 0
126387981 12638798 3 201512 0
126387981 12638798 5 201512 0