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
127307171 12730717 1 I 20110407 20110511 20160910 20160910 PER US-ASTRAZENECA-2011BM07411 ASTRAZENECA 24137.00 DY M Y 108.00000 KG 20160910 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
127307171 12730717 1 PS BYETTA EXENATIDE 1 Subcutaneous 0 U U 21773 5 UG SOLUTION FOR INJECTION IN PRE-FILLED PEN BID
127307171 12730717 2 SS BYETTA EXENATIDE 1 Subcutaneous 0 U U 21773 SOLUTION FOR INJECTION IN PRE-FILLED PEN
127307171 12730717 3 SS SYMBICORT BUDESONIDEFORMOTEROL FUMARATE DIHYDRATE 1 Respiratory (inhalation) Y U 0
127307171 12730717 4 SS BYDUREON EXENATIDE 1 Subcutaneous 0 2 MG /wk

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
127307171 12730717 1 Type 2 diabetes mellitus
127307171 12730717 2 Type 2 diabetes mellitus
127307171 12730717 3 Lung disorder

Outcome of event

no results found

Reactions reported

Event ID CASEID DRUG REC ACT PT
127307171 12730717 Blood glucose increased
127307171 12730717 Fungal infection
127307171 12730717 Product use issue
127307171 12730717 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
127307171 12730717 3 2015 201607 0
127307171 12730717 4 2015 0