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
101106372 10110637 2 F 20060309 20140305 20140425 20141231 EXP US-GSKPPD-2014GSK011130 GLAXOSMITHKLINE 65.38 YR M Y 0.00000 20141231 N MD COUNTRY NOT SPECIFIED 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
101106372 10110637 1 PS AVANDIA ROSIGLITAZONE MALEATE 1 ORAL DATES OF AVANDIA USE COULD NOT BE CONFIRMED IN RECORDS REVIEWED. D 21071 TABLETS
101106372 10110637 2 C LASIX FUROSEMIDE 1 D 0 40 MG
101106372 10110637 3 C COZAAR LOSARTAN POTASSIUM 1 D 0 50 MG
101106372 10110637 4 C TOPROL XL METOPROLOL SUCCINATE 1 D 0 50 MG
101106372 10110637 5 C VERAPAMIL VERAPAMIL HYDROCHLORIDE 1 D 0 180 MG

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
101106372 10110637 1 Diabetes mellitus

Outcome of event

Event ID CASEID OUTC COD
101106372 10110637 OT
101106372 10110637 HO

Reactions reported

Event ID CASEID DRUG REC ACT PT
101106372 10110637 Acute myocardial infarction
101106372 10110637 Cardiac failure congestive

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

no results found

Therapies reported

no results found