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
123386983 12338698 3 F 20160822 20160505 20160826 EXP US-GLAXOSMITHKLINE-US2016056490 GLAXOSMITHKLINE 0.00 F Y 0.00000 20160826 MD 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
123386983 12338698 1 PS COREG CR CARVEDILOL PHOSPHATE 1 Oral 40 MG, 1D U 5ZP1415 22012 40 MG QD
123386983 12338698 2 SS COREG CR CARVEDILOL PHOSPHATE 1 20 MG, BID U 22012 20 MG BID
123386983 12338698 3 C ASPIRIN. ASPIRIN 1 0
123386983 12338698 4 C BIOTIN BIOTIN 1 0
123386983 12338698 5 C FOLIC ACID. FOLIC ACID 1 0
123386983 12338698 6 C HYDRALAZINE HYDRALAZINE HYDROCHLORIDE 1 0
123386983 12338698 7 C HYDROCHLOROTHIAZIDE. HYDROCHLOROTHIAZIDE 1 0
123386983 12338698 8 C LASIX FUROSEMIDE 1 0
123386983 12338698 9 C PLAVIX CLOPIDOGREL BISULFATE 1 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
123386983 12338698 1 Myocardial infarction

Outcome of event

Event ID CASEID OUTC COD
123386983 12338698 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
123386983 12338698 Arrhythmia
123386983 12338698 Heart rate increased
123386983 12338698 Heart rate irregular
123386983 12338698 Therapeutic response decreased

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

no results found

Therapies reported

no results found