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
126903931 12690393 1 I 201602 20160329 20160826 20160826 PER US-FRI-1000083683 FOREST 66.71 YR F Y 67.60000 KG 20160826 CN US US

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
126903931 12690393 1 PS LEXAPRO ESCITALOPRAM OXALATE 1 Oral 10 MG Y U 21323 10 MG QD
126903931 12690393 2 SS LEXAPRO ESCITALOPRAM OXALATE 1 Oral 7.5 MG Y U 21323 7.5 MG QD
126903931 12690393 3 SS LEXAPRO ESCITALOPRAM OXALATE 1 Oral 5 MG Y U 0 5 MG QD
126903931 12690393 4 SS LEXAPRO ESCITALOPRAM OXALATE 1 Oral 2.5 MG Y U 0 2.5 MG QD
126903931 12690393 5 SS LEXAPRO ESCITALOPRAM OXALATE 1 Oral 5 MG Y U 0 5 MG QD

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
126903931 12690393 1 Generalised anxiety disorder

Outcome of event

no results found

Reactions reported

Event ID CASEID DRUG REC ACT PT
126903931 12690393 Abdominal pain upper
126903931 12690393 Anxiety
126903931 12690393 Defaecation urgency
126903931 12690393 Diarrhoea
126903931 12690393 Disturbance in attention
126903931 12690393 Gastrointestinal sounds abnormal
126903931 12690393 Intentional product use issue
126903931 12690393 Irritability
126903931 12690393 Nausea
126903931 12690393 Restlessness
126903931 12690393 Sleep disorder

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
126903931 12690393 1 2011 20160315 0
126903931 12690393 2 20160315 20160321 0
126903931 12690393 3 20160321 20160325 0
126903931 12690393 4 20160325 20160329 0
126903931 12690393 5 20160329 0