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
127937641 12793764 1 I 201411 20160913 20160929 20160929 EXP PHHY2016BR127523 NOVARTIS 90.12 YR F Y 68.00000 KG 20160929 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
127937641 12793764 1 PS EXELON PATCH RIVASTIGMINE 1 Transdermal 4.6 MG, QD (PATCH 5CM2) U 22083 4.6 MG TRANS-THERAPEUTIC-SYSTEM QD
127937641 12793764 2 SS EXELON PATCH RIVASTIGMINE 1 Transdermal 9.5 MG, QD (PATCH 10 CM2) U 22083 9.5 MG TRANS-THERAPEUTIC-SYSTEM QD
127937641 12793764 3 SS EXELON PATCH RIVASTIGMINE 1 Transdermal 13.3 MG, QD (PATCH 15CM2) U 22083 13.3 MG TRANS-THERAPEUTIC-SYSTEM QD
127937641 12793764 4 SS EXELON PATCH RIVASTIGMINE 1 Transdermal 9.5 MG, QD (PATCH 10CM2) U 22083 9.5 MG TRANS-THERAPEUTIC-SYSTEM QD

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
127937641 12793764 1 Dementia Alzheimer's type

Outcome of event

Event ID CASEID OUTC COD
127937641 12793764 OT
127937641 12793764 HO

Reactions reported

Event ID CASEID DRUG REC ACT PT
127937641 12793764 Abdominal pain
127937641 12793764 Asthenia
127937641 12793764 Diarrhoea
127937641 12793764 Gastrointestinal infection
127937641 12793764 Infection
127937641 12793764 Muscle spasms

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
127937641 12793764 3 201411 201411 0