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
126458412 12645841 2 F 20150912 20160809 20160811 20160816 EXP PHHY2016BR110041 NOVARTIS 72.61 YR M Y 0.00000 20160816 CN COUNTRY NOT SPECIFIED 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
126458412 12645841 1 PS EXELON PATCH RIVASTIGMINE 1 Transdermal 1 DF, QD 22083 1 DF TRANS-THERAPEUTIC-SYSTEM QD

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
126458412 12645841 1 Dementia Alzheimer's type

Outcome of event

Event ID CASEID OUTC COD
126458412 12645841 DE
126458412 12645841 HO

Reactions reported

Event ID CASEID DRUG REC ACT PT
126458412 12645841 Diplegia
126458412 12645841 Malaise
126458412 12645841 Metastases to spine
126458412 12645841 Metastatic neoplasm

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
126458412 12645841 1 201507 201509 0