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
101114662 10111466 2 F 19990217 20140305 20140425 20141231 EXP US-GSKPPD-2014GSK010821 GLAXOSMITHKLINE 56.40 YR F Y 103.51000 KG 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
101114662 10111466 1 PS AVANDIA ROSIGLITAZONE MALEATE 1 ORAL AVANDIA WAS NOT LISTED AMONG THE PATIENTS ADMISSION OR DISCHARGE RECORDS. D 21071 TABLETS
101114662 10111466 2 C NITROGLYCERIN. NITROGLYCERIN 1 SUBLINGUAL D 0
101114662 10111466 3 C ASPIRIN. ASPIRIN 1 D 0 325 MG
101114662 10111466 4 C LOPRESSOR METOPROLOL TARTRATE 1 D 0 50 MG
101114662 10111466 5 C LASIX FUROSEMIDE 1 D 0 40 MG
101114662 10111466 6 C LIPITOR ATORVASTATIN CALCIUM 1 D 0 20 MG

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
101114662 10111466 1 Diabetes mellitus

Outcome of event

Event ID CASEID OUTC COD
101114662 10111466 HO
101114662 10111466 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
101114662 10111466 Coronary artery occlusion

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

no results found

Therapies reported

no results found