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
125463071 12546307 1 I 2016 20160701 20160711 20160711 EXP PHHY2016BR093251 NOVARTIS 0.00 M Y 0.00000 20160711 OT BR BR

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
125463071 12546307 1 PS EXELON PATCH RIVASTIGMINE 1 Transdermal 4.6 MG (PATCH 5 CM2), QD 674140 22083 4.6 MG TRANS-THERAPEUTIC-SYSTEM QD
125463071 12546307 2 SS EXELON PATCH RIVASTIGMINE 1 22083 TRANS-THERAPEUTIC-SYSTEM
125463071 12546307 3 C GINKGO BILOBA GINKGO 1 Unknown U 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
125463071 12546307 1 Memory impairment
125463071 12546307 2 Dementia Alzheimer's type
125463071 12546307 3 Product used for unknown indication

Outcome of event

Event ID CASEID OUTC COD
125463071 12546307 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
125463071 12546307 Abnormal behaviour
125463071 12546307 Blood pressure decreased
125463071 12546307 Constipation
125463071 12546307 Dementia Alzheimer's type
125463071 12546307 Fall
125463071 12546307 Gastrointestinal disorder
125463071 12546307 Malaise
125463071 12546307 Saliva altered
125463071 12546307 Salivary hypersecretion
125463071 12546307 Speech disorder
125463071 12546307 Syncope

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
125463071 12546307 1 201604 0