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
126976171 12697617 1 I 20160816 20160830 20160830 EXP PHHY2016BR113777 NOVARTIS 0.00 F Y 75.00000 KG 20160830 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
126976171 12697617 1 PS EXELON PATCH RIVASTIGMINE 1 Transdermal PATCH 5 CM2 U 22083 4.6 MG TRANS-THERAPEUTIC-SYSTEM QD
126976171 12697617 2 SS EXELON PATCH RIVASTIGMINE 1 Transdermal PATCH 10 CM2 U 22083 9.5 MG TRANS-THERAPEUTIC-SYSTEM QD
126976171 12697617 3 SS EXELON PATCH RIVASTIGMINE 1 Transdermal PATCH 15 CM2 U 22083 13.3 MG TRANS-THERAPEUTIC-SYSTEM QD
126976171 12697617 4 SS EXELON RIVASTIGMINE TARTRATE 1 Unknown 0 TABLET

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
126976171 12697617 1 Dementia Alzheimer's type
126976171 12697617 4 Dementia Alzheimer's type

Outcome of event

Event ID CASEID OUTC COD
126976171 12697617 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
126976171 12697617 Asthenia
126976171 12697617 Depressed mood
126976171 12697617 Epigastric discomfort
126976171 12697617 Fall
126976171 12697617 Fear
126976171 12697617 Mobility decreased
126976171 12697617 Nausea
126976171 12697617 Panic disorder
126976171 12697617 Syncope
126976171 12697617 Vomiting
126976171 12697617 Weight decreased

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

no results found

Therapies reported

no results found