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
127688411 12768841 1 I 201607 20160822 20160921 20160921 EXP PHJP2016JP023577 NOVARTIS 89.00 YR F Y 0.00000 20160921 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
127688411 12768841 1 PS EXELON PATCH RIVASTIGMINE 1 Transdermal 4.6 MG, QD (9 MG RIVASTIGMINE BASE, PATCH 5 CM2) 22083 4.6 MG TRANS-THERAPEUTIC-SYSTEM QD
127688411 12768841 2 SS EXELON PATCH RIVASTIGMINE 1 Transdermal 9.5 MG, QD (18 MG RIVASTIGMINE BASE, PATCH 10 CM2) 22083 9.5 MG TRANS-THERAPEUTIC-SYSTEM QD

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
127688411 12768841 1 Dementia Alzheimer's type

Outcome of event

Event ID CASEID OUTC COD
127688411 12768841 HO

Reactions reported

Event ID CASEID DRUG REC ACT PT
127688411 12768841 Fall
127688411 12768841 Fracture
127688411 12768841 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
127688411 12768841 1 201512 0
127688411 12768841 2 201602 0