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
126675691 12667569 1 I 20160808 20160819 20160819 PER US-TAKEDA-2016TUS014274 TAKEDA 0.00 A Y 0.00000 20160819 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
126675691 12667569 1 PS BRINTELLIX VORTIOXETINE HYDROBROMIDE 1 Unknown 5 MG, UNK U UNKNOWN 204447 5 MG TABLET
126675691 12667569 2 SS BRINTELLIX VORTIOXETINE HYDROBROMIDE 1 Unknown 10 MG, UNK U UNKNOWN 204447 10 MG TABLET
126675691 12667569 3 SS BRINTELLIX VORTIOXETINE HYDROBROMIDE 1 Unknown 20 MG, UNK U UNKNOWN 204447 20 MG TABLET
126675691 12667569 4 SS LEXAPRO ESCITALOPRAM OXALATE 1 Unknown 20 MG, UNK UNK 0 20 MG

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
126675691 12667569 1 Depression
126675691 12667569 2 Generalised anxiety disorder
126675691 12667569 4 Product used for unknown indication

Outcome of event

no results found

Reactions reported

Event ID CASEID DRUG REC ACT PT
126675691 12667569 Anxiety
126675691 12667569 Dizziness
126675691 12667569 Dysstasia
126675691 12667569 Feeling abnormal
126675691 12667569 Speech disorder
126675691 12667569 Tremor

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

no results found

Therapies reported

no results found