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
126698511 12669851 1 I 20160812 20160819 20160819 EXP PHHY2016BR113776 NOVARTIS 0.00 F Y 66.00000 KG 20160819 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
126698511 12669851 1 PS EXELON PATCH RIVASTIGMINE 1 Transdermal PATCH 5CM2, QD 22083 4.6 MG TRANS-THERAPEUTIC-SYSTEM QD
126698511 12669851 2 SS EXELON PATCH RIVASTIGMINE 1 Transdermal PATCH 10CM2, QD 651210 22083 9.5 MG TRANS-THERAPEUTIC-SYSTEM QD
126698511 12669851 3 SS EXELON PATCH RIVASTIGMINE 1 Transdermal PATCH 15CM2, QD 22083 13.3 MG TRANS-THERAPEUTIC-SYSTEM QD
126698511 12669851 4 SS EXELON PATCH RIVASTIGMINE 1 Transdermal PATCH 10CM2, QD 22083 9.5 MG TRANS-THERAPEUTIC-SYSTEM QD

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
126698511 12669851 1 Vascular dementia

Outcome of event

Event ID CASEID OUTC COD
126698511 12669851 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
126698511 12669851 Condition aggravated
126698511 12669851 Drug ineffective
126698511 12669851 Product use issue
126698511 12669851 Vascular dementia

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
126698511 12669851 1 2013 0