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
125506072 12550607 2 F 20160707 20160712 20160715 EXP DK-FRI-1000085955 FOREST 0.00 F Y 0.00000 20160715 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
125506072 12550607 1 PS ESCITALOPRAM ESCITALOPRAM OXALATE 1 Unknown U 21323
125506072 12550607 2 SS BRINTELLIX VORTIOXETINE HYDROBROMIDE 1 Unknown Y 0 5 MG

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
125506072 12550607 1 Major depression
125506072 12550607 2 Major depression

Outcome of event

Event ID CASEID OUTC COD
125506072 12550607 HO

Reactions reported

Event ID CASEID DRUG REC ACT PT
125506072 12550607 Aggression
125506072 12550607 Confusional state
125506072 12550607 Drug ineffective
125506072 12550607 Feeling abnormal
125506072 12550607 Limb discomfort
125506072 12550607 Muscle spasms

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
125506072 12550607 1 20160329 20160418 0
125506072 12550607 2 20160418 20160512 0