The Safety Rates Drug Report

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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
124729732 12472973 2 F 20160317 20160713 20160616 20160714 PER JP-EISAI MEDICAL RESEARCH-EC-2016-017705 EISAI 85.00 YR M Y 0.00000 20160714 MD 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
124729732 12472973 1 PS ARICEPT DONEPEZIL HYDROCHLORIDE 1 Oral Y 20690 3 MG TABLET QD
124729732 12472973 2 SS ARICEPT DONEPEZIL HYDROCHLORIDE 1 Oral Y 20690 5 MG TABLET QD
124729732 12472973 3 SS ARICEPT DONEPEZIL HYDROCHLORIDE 1 Oral Y 20690 3 MG TABLET QD
124729732 12472973 4 C MEMARY MEMANTINE HYDROCHLORIDE 1 0
124729732 12472973 5 C SEROQUEL QUETIAPINE FUMARATE 1 0
124729732 12472973 6 C NU-LOTAN LOSARTAN POTASSIUM 1 0
124729732 12472973 7 C LIPITOR ATORVASTATIN CALCIUM 1 0
124729732 12472973 8 C MUCOSTA REBAMIPIDE 1 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
124729732 12472973 1 Dementia with Lewy bodies

Outcome of event

no results found

Reactions reported

Event ID CASEID DRUG REC ACT PT
124729732 12472973 Anger

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
124729732 12472973 1 20160302 20160314 0
124729732 12472973 2 20160315 20160321 0
124729732 12472973 3 20160322 20160329 0