The Safety Rates Drug Report

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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
125035872 12503587 2 F 201606 20160708 20160628 20160712 EXP PHJP2016JP016136 NOVARTIS 82.00 YR M Y 0.00000 20160712 PH JP JP

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
125035872 12503587 1 PS EXELON PATCH RIVASTIGMINE 1 Transdermal 9 MG (PATCH5, 4.6MG/24H) Y 22083 9 MG TRANS-THERAPEUTIC-SYSTEM QD
125035872 12503587 2 SS SERMION NICERGOLINE 1 Oral 2 DF, BID Y U 0 2 DF TABLET BID
125035872 12503587 3 SS RISPERDAL RISPERIDONE 1 Unknown UNK Y U 0
125035872 12503587 4 SS HALCION TRIAZOLAM 1 Oral 0.15 MG, UNK Y U 0 .15 MG TABLET

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
125035872 12503587 1 Dementia Alzheimer's type
125035872 12503587 2 Product used for unknown indication
125035872 12503587 3 Product used for unknown indication
125035872 12503587 4 Product used for unknown indication

Outcome of event

no results found

Reactions reported

Event ID CASEID DRUG REC ACT PT
125035872 12503587 Concomitant disease progression
125035872 12503587 Decreased appetite

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
125035872 12503587 1 20160610 20160615 0