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
125463322 12546332 2 F 20160705 20160809 20160711 20160810 EXP PHJP2016JP019400 NOVARTIS 78.00 YR F Y 0.00000 20160810 MD 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
125463322 12546332 1 PS EXELON PATCH RIVASTIGMINE 1 Transdermal 4.6 MG, QD (PATCH5(CM2), DAILY) Y 22083 4.6 MG TRANS-THERAPEUTIC-SYSTEM QD
125463322 12546332 2 SS EXELON PATCH RIVASTIGMINE 1 Transdermal 9.5 MG, QD (PATCH10(CM2), DAILY) Y 22083 9.5 MG TRANS-THERAPEUTIC-SYSTEM QD
125463322 12546332 3 SS EXELON PATCH RIVASTIGMINE 1 Transdermal 8 DF, QD (8 X (PATCH5(CM2), DAILY)) Y 22083 8 DF TRANS-THERAPEUTIC-SYSTEM QD

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
125463322 12546332 1 Dementia Alzheimer's type

Outcome of event

Event ID CASEID OUTC COD
125463322 12546332 HO

Reactions reported

Event ID CASEID DRUG REC ACT PT
125463322 12546332 Epilepsy
125463322 12546332 Vomiting
125463322 12546332 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

Event ID CASEID DSG DRUG SEQ START DT END DT DUR DUR COD
125463322 12546332 1 20151130 0
125463322 12546332 3 20160705 20160705 0