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
125766521 12576652 1 I 201607 20160712 20160720 20160720 PER US-EISAI MEDICAL RESEARCH-EC-2016-018528 EISAI 88.00 YR M Y 0.00000 20160720 CN US US

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
125766521 12576652 1 PS ARICEPT DONEPEZIL HYDROCHLORIDE 1 Oral 20690 5 MG TABLET QD
125766521 12576652 2 SS ARICEPT DONEPEZIL HYDROCHLORIDE 1 Oral 20690 10 MG TABLET QD
125766521 12576652 3 SS ARICEPT DONEPEZIL HYDROCHLORIDE 1 Oral 20690 10 MG TABLET QD
125766521 12576652 4 C ZOCOR SIMVASTATIN 1 0
125766521 12576652 5 C PRILOSEC OMEPRAZOLE MAGNESIUM 1 0
125766521 12576652 6 C CELEBREX CELECOXIB 1 0
125766521 12576652 7 C SYNTHROID LEVOTHYROXINE SODIUM 1 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
125766521 12576652 1 Dementia
125766521 12576652 5 Gastrooesophageal reflux disease
125766521 12576652 7 Hypothyroidism

Outcome of event

no results found

Reactions reported

Event ID CASEID DRUG REC ACT PT
125766521 12576652 Hypertension

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
125766521 12576652 1 2008 0
125766521 12576652 2 201601 0
125766521 12576652 3 20160703 0