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
126804851 12680485 1 I 20160101 20160818 20160824 20160824 EXP PHHY2016BR115723 NOVARTIS 83.95 YR F Y 67.00000 KG 20160824 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
126804851 12680485 1 PS EXELON PATCH RIVASTIGMINE 1 Transdermal PATCH 5 (CM2), UNK 22083 4.6 MG TRANS-THERAPEUTIC-SYSTEM
126804851 12680485 2 SS EXELON PATCH RIVASTIGMINE 1 Transdermal PATCH 10 (CM2), UNK 22083 9.5 MG TRANS-THERAPEUTIC-SYSTEM
126804851 12680485 3 SS EXELON PATCH RIVASTIGMINE 1 Transdermal PATCH 15 (CM2), QD 615660 22083 13.3 MG TRANS-THERAPEUTIC-SYSTEM QD
126804851 12680485 4 SS PROLOPA BENSERAZIDELEVODOPA 1 Unknown Y 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
126804851 12680485 1 Cognitive disorder
126804851 12680485 2 Dementia
126804851 12680485 3 Cognitive disorder
126804851 12680485 4 Product used for unknown indication

Outcome of event

Event ID CASEID OUTC COD
126804851 12680485 HO

Reactions reported

Event ID CASEID DRUG REC ACT PT
126804851 12680485 Confusional state
126804851 12680485 Fall
126804851 12680485 Femur fracture
126804851 12680485 Hallucination
126804851 12680485 Illusion
126804851 12680485 Memory impairment
126804851 12680485 Nervousness
126804851 12680485 Spinal fracture

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
126804851 12680485 3 20160811 0