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
126714891 12671489 1 I 20160817 20160822 20160822 EXP PHHY2016BR114475 NOVARTIS 0.00 F Y 0.00000 20160822 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
126714891 12671489 1 PS EXELON PATCH RIVASTIGMINE 1 Transdermal PATCH 10 (CM2), UNK 22083 9.5 MG TRANS-THERAPEUTIC-SYSTEM

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
126714891 12671489 1 Dementia Alzheimer's type

Outcome of event

Event ID CASEID OUTC COD
126714891 12671489 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
126714891 12671489 Abasia
126714891 12671489 Choking
126714891 12671489 Drug ineffective
126714891 12671489 Eating disorder
126714891 12671489 Malaise
126714891 12671489 Pneumonia aspiration
126714891 12671489 Speech disorder

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

no results found

Therapies reported

no results found