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
127098331 12709833 1 I 2016 20160829 20160902 20160902 EXP PHHY2016BR120221 NOVARTIS 0.00 F Y 55.00000 KG 20160902 MD 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
127098331 12709833 1 PS EXELON PATCH RIVASTIGMINE 1 Transdermal PATCH 5 CM2 N 22083 4.6 MG TRANS-THERAPEUTIC-SYSTEM
127098331 12709833 2 SS EXELON PATCH RIVASTIGMINE 1 Transdermal PATCH 10 CM2 N 22083 9.5 MG TRANS-THERAPEUTIC-SYSTEM
127098331 12709833 3 SS EXELON PATCH RIVASTIGMINE 1 Transdermal PATCH 15 CM2 N 22083 13.3 MG TRANS-THERAPEUTIC-SYSTEM

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
127098331 12709833 1 Dementia Alzheimer's type
127098331 12709833 2 Parkinson's disease

Outcome of event

Event ID CASEID OUTC COD
127098331 12709833 HO

Reactions reported

Event ID CASEID DRUG REC ACT PT
127098331 12709833 Diarrhoea
127098331 12709833 Discomfort
127098331 12709833 Drug intolerance
127098331 12709833 Feeling abnormal
127098331 12709833 Hypersensitivity
127098331 12709833 Vomiting

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
127098331 12709833 1 201602 0
127098331 12709833 2 201604 0
127098331 12709833 3 201606 0