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
126862021 12686202 1 I 20160810 20160825 20160825 EXP PHHY2016BR110696 NOVARTIS 0.00 F Y 56.00000 KG 20160825 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
126862021 12686202 1 PS EXELON PATCH RIVASTIGMINE 1 Transdermal PATCH 10 (CM2), QD 22083 9.5 MG TRANS-THERAPEUTIC-SYSTEM QD
126862021 12686202 2 C HEIMER MEMANTINE HYDROCHLORIDE 1 Oral 2 TABLETS A DAY, ORALLY 0 1 DF TABLET BID

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
126862021 12686202 1 Dementia Alzheimer's type
126862021 12686202 2 Dementia Alzheimer's type

Outcome of event

Event ID CASEID OUTC COD
126862021 12686202 OT
126862021 12686202 HO

Reactions reported

Event ID CASEID DRUG REC ACT PT
126862021 12686202 Decreased immune responsiveness
126862021 12686202 Herpes zoster
126862021 12686202 Weight decreased

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
126862021 12686202 1 201410 20160808 0
126862021 12686202 2 201410 0