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
126907161 12690716 1 I 2016 20160621 20160826 20160826 PER US-ASTRAZENECA-2016SE69234 ASTRAZENECA 87.00 YR F Y 73.50000 KG 20160826 CN 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
126907161 12690716 1 PS BYDUREON EXENATIDE 1 Subcutaneous 418 MG FM0250 22200 2 MG /wk
126907161 12690716 2 SS BYETTA EXENATIDE 1 Unknown 0 SOLUTION FOR INJECTION IN PRE-FILLED PEN
126907161 12690716 3 SS LISINOPRIL. LISINOPRIL 1 Oral DAILY 0 TABLET
126907161 12690716 4 C SIMVASTATIN. SIMVASTATIN 1 Oral DAILY 0
126907161 12690716 5 C SYNTHROID LEVOTHYROXINE SODIUM 1 Oral DAILY 0
126907161 12690716 6 C ALLOPURINOL. ALLOPURINOL 1 Oral 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
126907161 12690716 1 Type 2 diabetes mellitus
126907161 12690716 2 Type 2 diabetes mellitus
126907161 12690716 3 Diabetes mellitus
126907161 12690716 4 Blood cholesterol increased
126907161 12690716 5 Hypothyroidism
126907161 12690716 6 Blood uric acid increased

Outcome of event

no results found

Reactions reported

Event ID CASEID DRUG REC ACT PT
126907161 12690716 Blood glucose increased
126907161 12690716 Cystitis
126907161 12690716 Injection site extravasation
126907161 12690716 Underdose

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
126907161 12690716 1 2012 0