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
126099461 12609946 1 I 20160725 0 20160729 20160729 DIR 74.00 YR F N 100.10000 KG 20160728 N PH 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
126099461 12609946 1 PS PRADAXA DABIGATRAN ETEXILATE MESYLATE 1 Oral Y D 0 150 MG BID
126099461 12609946 2 SS MULTAQ DRONEDARONE 1 Oral Y D 0 400 MG BID
126099461 12609946 4 C AMLODIPINE AMLODIPINE BESYLATE 1 0
126099461 12609946 6 C CHOLECALCIFEROL CHOLECALCIFEROL 1 0
126099461 12609946 8 C GLIMEPIRIDE. GLIMEPIRIDE 1 0
126099461 12609946 10 C HYDROCHLOROTHIAZIDE. HYDROCHLOROTHIAZIDE 1 0
126099461 12609946 12 C LISINOPRIL. LISINOPRIL 1 0
126099461 12609946 14 C PRAVASTATIN. PRAVASTATIN 1 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
126099461 12609946 1 Atrial fibrillation
126099461 12609946 2 Atrial fibrillation

Outcome of event

Event ID CASEID OUTC COD
126099461 12609946 HO

Reactions reported

Event ID CASEID DRUG REC ACT PT
126099461 12609946 Drug interaction
126099461 12609946 Fall
126099461 12609946 Haematoma
126099461 12609946 Incorrect dose administered

Reporting Sources (this data is often not reported and may therefore be missing here)

Event ID CASEID RPSR COD
126099461 12609946 HP

Therapies reported

no results found