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
126224492 12622449 2 F 20160718 20160804 20160804 20160809 EXP PHHY2016JP106712 NOVARTIS 78.00 YR F Y 0.00000 20160809 CN JP JP

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
126224492 12622449 1 PS RIVASTACH RIVASTIGMINE 1 Transdermal UNK Y 22083 TRANS-THERAPEUTIC-SYSTEM
126224492 12622449 2 SS RIVASTACH RIVASTIGMINE 1 Transdermal 54 MG (SIX 9 MG PATCHES) Y 22083 54 MG TRANS-THERAPEUTIC-SYSTEM
126224492 12622449 3 SS ARICEPT DONEPEZIL HYDROCHLORIDE 1 Oral UNK U 0 TABLET

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
126224492 12622449 1 Dementia Alzheimer's type
126224492 12622449 3 Dementia Alzheimer's type

Outcome of event

Event ID CASEID OUTC COD
126224492 12622449 HO
126224492 12622449 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
126224492 12622449 Nausea
126224492 12622449 Neuroleptic malignant syndrome
126224492 12622449 Overdose
126224492 12622449 Treatment noncompliance
126224492 12622449 Vomiting
126224492 12622449 Wrong technique in product usage process

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
126224492 12622449 2 201607 0
126224492 12622449 3 2015 0