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
121902725 12190272 5 F 201602 20160817 20160318 20160823 EXP PHHY2016PA036343 NOVARTIS 90.15 YR F Y 0.00000 20160823 CN COUNTRY NOT SPECIFIED PA

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
121902725 12190272 1 PS EXELON PATCH RIVASTIGMINE 1 Transdermal UNK U 22083 TRANS-THERAPEUTIC-SYSTEM

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
121902725 12190272 1 Dementia Alzheimer's type

Outcome of event

Event ID CASEID OUTC COD
121902725 12190272 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
121902725 12190272 Abasia
121902725 12190272 Alopecia
121902725 12190272 Blood glucose increased
121902725 12190272 Blood sodium decreased
121902725 12190272 Brain hypoxia
121902725 12190272 Contusion
121902725 12190272 Decreased activity
121902725 12190272 Dyspnoea
121902725 12190272 Fall
121902725 12190272 Hallucination, visual
121902725 12190272 Ischaemic stroke
121902725 12190272 Jaundice
121902725 12190272 Middle insomnia
121902725 12190272 Pruritus generalised
121902725 12190272 Speech disorder
121902725 12190272 Transient ischaemic attack
121902725 12190272 Tremor
121902725 12190272 Yellow skin

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

no results found

Therapies reported

no results found