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
124617543 12461754 3 F 201512 20160909 20160613 20160915 EXP US-PFIZER INC-2016295067 PFIZER 66.00 YR F Y 0.00000 20160915 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
124617543 12461754 1 PS EFFEXOR XR VENLAFAXINE HYDROCHLORIDE 1 UNK N 20699 PROLONGED-RELEASE CAPSULE
124617543 12461754 2 SS PRISTIQ EXTENDED-RELEASE DESVENLAFAXINE SUCCINATE 1 50 MG, 1X/DAY 21992 50 MG PROLONGED-RELEASE TABLET QD
124617543 12461754 3 C BUPROPION. BUPROPION 1 UNK 0
124617543 12461754 4 C SINGULAIR MONTELUKAST SODIUM 1 UNK 0
124617543 12461754 5 C LEVOTHYROXINE. LEVOTHYROXINE 1 UNK 0
124617543 12461754 6 C NUCYNTA TAPENTADOL HYDROCHLORIDE 1 UNK 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
124617543 12461754 1 Major depression
124617543 12461754 2 Depression

Outcome of event

Event ID CASEID OUTC COD
124617543 12461754 HO
124617543 12461754 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
124617543 12461754 Atrial fibrillation
124617543 12461754 Electrocardiogram QT prolonged

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
124617543 12461754 1 2000 2014 0
124617543 12461754 2 2014 0
124617543 12461754 3 2010 0
124617543 12461754 4 2010 0
124617543 12461754 5 2008 0
124617543 12461754 6 2013 0