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
126190513 12619051 3 F 20160807 20160822 20160803 20160826 EXP PHHY2016BR105181 NOVARTIS 90.00 YR M Y 0.00000 20160826 CN 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
126190513 12619051 1 PS EXELON PATCH RIVASTIGMINE 1 Transdermal 4.6 MG (PATCH: 9 MG/5 CM2, 30 PATCHES), QD Y U 22083 4.6 MG TRANS-THERAPEUTIC-SYSTEM QD

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
126190513 12619051 1 Senile dementia

Outcome of event

Event ID CASEID OUTC COD
126190513 12619051 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
126190513 12619051 Abasia
126190513 12619051 Aphasia
126190513 12619051 Constipation
126190513 12619051 Dementia
126190513 12619051 Dysarthria
126190513 12619051 Dyspnoea
126190513 12619051 Fall
126190513 12619051 Fatigue
126190513 12619051 Feeding disorder
126190513 12619051 Hallucination
126190513 12619051 Memory impairment
126190513 12619051 Muscular weakness
126190513 12619051 Oral discharge
126190513 12619051 Product use issue
126190513 12619051 Saliva altered
126190513 12619051 Urinary incontinence

Reporting Sources (this data is often not reported and may therefore be missing here)

no results found

Therapies reported

no results found