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
127465051 12746505 1 I 20160909 20160915 20160915 EXP PHHY2016BR126868 NOVARTIS 0.00 F Y 0.00000 20160915 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
127465051 12746505 1 PS EXELON PATCH RIVASTIGMINE 1 Transdermal 4.6 MG, QD PATCH 5 (CM2) 719130 22083 4.6 MG TRANS-THERAPEUTIC-SYSTEM QD

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
127465051 12746505 1 Product used for unknown indication

Outcome of event

Event ID CASEID OUTC COD
127465051 12746505 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
127465051 12746505 Drug intolerance
127465051 12746505 Drug prescribing error
127465051 12746505 Incorrect product storage
127465051 12746505 Parkinsonian crisis
127465051 12746505 Weight increased
127465051 12746505 Wrong technique in product usage process

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

no results found

Therapies reported

no results found