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
125918891 12591889 1 I 20150816 20160719 20160726 20160726 EXP PHHY2016BR100715 NOVARTIS 85.47 YR F Y 69.00000 KG 20160726 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
125918891 12591889 1 PS EXELON PATCH RIVASTIGMINE 1 Transdermal PATCH 10 CM2 U 22083 9.5 MG TRANS-THERAPEUTIC-SYSTEM
125918891 12591889 2 SS EXELON PATCH RIVASTIGMINE 1 Transdermal PATCH 5 CM2 U 22083 4.6 MG TRANS-THERAPEUTIC-SYSTEM
125918891 12591889 3 SS EXELON PATCH RIVASTIGMINE 1 Transdermal PATCH 10 CM2 U 22083 9.5 MG TRANS-THERAPEUTIC-SYSTEM

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
125918891 12591889 1 Dementia Alzheimer's type

Outcome of event

Event ID CASEID OUTC COD
125918891 12591889 HO

Reactions reported

Event ID CASEID DRUG REC ACT PT
125918891 12591889 Malaise
125918891 12591889 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
125918891 12591889 1 20150815 20150817 0
125918891 12591889 2 2016 0