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
127112051 12711205 1 I 2014 20160826 20160902 20160902 EXP DK-DKMA-WBS-0004351 DK-FRI-1000087231 FOREST 0.00 M Y 0.00000 20160902 OT DK DK

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
127112051 12711205 1 PS ESCITALOPRAM ESCITALOPRAM OXALATE 1 Oral Y U HAVES IKKE 21323 FILM-COATED TABLET
127112051 12711205 2 SS ESCITALOPRAM ESCITALOPRAM OXALATE 1 Unknown Y U HAVES IKKE 21323
127112051 12711205 3 C MIANSERIN MIANSERIN 1 Unknown 0 10 MG

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
127112051 12711205 1 Obsessive-compulsive disorder
127112051 12711205 3 Obsessive-compulsive disorder

Outcome of event

Event ID CASEID OUTC COD
127112051 12711205 DS

Reactions reported

Event ID CASEID DRUG REC ACT PT
127112051 12711205 Headache
127112051 12711205 Photopsia
127112051 12711205 Pollakiuria
127112051 12711205 Visual impairment

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
127112051 12711205 1 2006 201406 0
127112051 12711205 2 201505 0
127112051 12711205 3 2006 0