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
126209831 12620983 1 I 20160801 0 20160803 20160803 DIR 83.00 YR M N 170.00000 LBS 20160802 N 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
126209831 12620983 1 PS TRICOR FENOFIBRATE 1 Oral Y D 0 30 DF COATED TABLET QD
126209831 12620983 3 C COREG CARVEDILOL 1 0
126209831 12620983 5 C OMEPRAZOLE. OMEPRAZOLE 1 0
126209831 12620983 7 C SPIRONOLACTONE. SPIRONOLACTONE 1 0
126209831 12620983 9 C TIKOSYN DOFETILIDE 1 0
126209831 12620983 11 C WARFARIN WARFARIN 1 0
126209831 12620983 13 C ZOCOR SIMVASTATIN 1 0
126209831 12620983 15 C DIGOXIN. DIGOXIN 1 0
126209831 12620983 17 C TYLENOL ACETAMINOPHEN 1 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
126209831 12620983 1 Blood triglycerides increased

Outcome of event

Event ID CASEID OUTC COD
126209831 12620983 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
126209831 12620983 Atrial fibrillation
126209831 12620983 Drug interaction

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
126209831 12620983 1 20160727 20160731 0