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
124655433 12465543 3 F 2016 20160707 20160614 20160715 EXP CA-PFIZER INC-2016294924 PFIZER 83.00 YR F Y 0.00000 20160715 PH CA CA

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
124655433 12465543 1 PS TOVIAZ FESOTERODINE FUMARATE 1 Oral 4 MG, 1X/DAY 22030 4 MG PROLONGED-RELEASE TABLET QD
124655433 12465543 2 SS ARICEPT DONEPEZIL HYDROCHLORIDE 1 Oral 5 MG, 1X/DAY 0 5 MG PROLONGED-RELEASE TABLET QD
124655433 12465543 3 SS ARICEPT DONEPEZIL HYDROCHLORIDE 1 10 MG, 1X/DAY 0 10 MG PROLONGED-RELEASE TABLET QD
124655433 12465543 4 SS NAPROXEN SODIUM. NAPROXEN SODIUM 1 Oral 250 MG, 2X/DAY AND AS NEEDED 0 250 MG
124655433 12465543 5 SS NAPROXEN SODIUM. NAPROXEN SODIUM 1 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
124655433 12465543 1 Pollakiuria
124655433 12465543 2 Dementia
124655433 12465543 4 Inflammation
124655433 12465543 5 Pain

Outcome of event

Event ID CASEID OUTC COD
124655433 12465543 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
124655433 12465543 Condition aggravated
124655433 12465543 Dementia

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
124655433 12465543 1 20160220 0
124655433 12465543 2 20150909 20151009 0
124655433 12465543 3 201510 0
124655433 12465543 4 2007 0