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
123896134 12389613 4 F 2016 20160815 20160520 20160817 EXP US-PFIZER INC-2016266083 PFIZER 67.00 YR F Y 61.23000 KG 20160817 OT 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
123896134 12389613 1 PS EFFEXOR XR VENLAFAXINE HYDROCHLORIDE 1 Oral 225 MG (150 MG PLUS 75 MG), 1X/DAY 20699 225 MG PROLONGED-RELEASE CAPSULE QD
123896134 12389613 2 C AMLODIPINE AMLODIPINE BESYLATE 1 5 MG, 1X/DAY(EVERY MORNING) 0 5 MG QD
123896134 12389613 3 C ATORVASTATIN ATORVASTATIN 1 20 MG, 1X/DAY(AT BEDTIME) 0 20 MG QD

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
123896134 12389613 1 Depression
123896134 12389613 2 Hypertension
123896134 12389613 3 Blood cholesterol increased

Outcome of event

Event ID CASEID OUTC COD
123896134 12389613 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
123896134 12389613 Incontinence
123896134 12389613 Nephrolithiasis
123896134 12389613 Urinary tract infection

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
123896134 12389613 1 2008 0
123896134 12389613 2 2011 0
123896134 12389613 3 2011 0