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
125303092 12530309 2 F 20160624 20160706 20160714 PER US-ASTRAZENECA-2015SF04098 ASTRAZENECA 26387.00 DY F Y 136.10000 KG 20160714 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
125303092 12530309 1 PS BYETTA EXENATIDE 1 Subcutaneous 10.0UG UNKNOWN 21773 10 UG SOLUTION FOR INJECTION IN PRE-FILLED PEN
125303092 12530309 2 C COUMANDIN 2 Oral 0 5 MG QD
125303092 12530309 3 C LOPRESSURE TARTRATE 2 Oral 50.0MG UNKNOWN 0 50 MG
125303092 12530309 4 C LASIX FUROSEMIDE 1 Oral 40.0MG UNKNOWN 0 40 MG
125303092 12530309 5 C POTASSIUM POTASSIUM 1 Oral 0 10 MEQ QD

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
125303092 12530309 1 Diabetes mellitus
125303092 12530309 2 Atrial fibrillation
125303092 12530309 3 Blood pressure abnormal
125303092 12530309 4 Blood pressure abnormal
125303092 12530309 5 Diuretic therapy

Outcome of event

no results found

Reactions reported

Event ID CASEID DRUG REC ACT PT
125303092 12530309 Product quality issue
125303092 12530309 Weight decreased

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
125303092 12530309 1 2006 0
125303092 12530309 2 2008 0