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
126473162 12647316 2 F 201606 20160809 20160812 20160816 EXP PHHY2016BR110108 NOVARTIS 91.32 YR F Y 52.00000 KG 20160816 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
126473162 12647316 1 PS EXELON PATCH RIVASTIGMINE 1 Transdermal 4.6 MG [PATCH 5 (CM) 2], QD Y 22083 4.6 MG TRANS-THERAPEUTIC-SYSTEM QD
126473162 12647316 2 SS EXELON PATCH RIVASTIGMINE 1 Transdermal 9.5 MG [PATCH 10 (CM) 2], QD Y 22083 9.5 MG TRANS-THERAPEUTIC-SYSTEM QD
126473162 12647316 3 SS EXELON PATCH RIVASTIGMINE 1 Transdermal 13.3 MG [PATCH 15 (CM) 2], QD Y 22083 13.3 MG TRANS-THERAPEUTIC-SYSTEM QD
126473162 12647316 4 SS EXELON PATCH RIVASTIGMINE 1 Transdermal 4.6 MG [PATCH 5 (CM) 2], QD Y 22083 4.6 MG TRANS-THERAPEUTIC-SYSTEM QD

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
126473162 12647316 1 Dementia Alzheimer's type

Outcome of event

Event ID CASEID OUTC COD
126473162 12647316 HO
126473162 12647316 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
126473162 12647316 Abasia
126473162 12647316 Balance disorder
126473162 12647316 Blood pressure increased
126473162 12647316 Dysstasia
126473162 12647316 Malaise
126473162 12647316 Speech disorder
126473162 12647316 Urinary tract infection
126473162 12647316 Vomiting

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
126473162 12647316 3 201605 0
126473162 12647316 4 20160725 0