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
126699592 12669959 2 F 20150629 20160623 20160820 20160909 EXP CN-ASTRAZENECA-2016SE60856 ASTRAZENECA 29.00 YR F Y 41.00000 KG 20160909 CN CN CN

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
126699592 12669959 1 PS BYETTA EXENATIDE 1 Subcutaneous U U 21773 10 UG SOLUTION FOR INJECTION IN PRE-FILLED PEN BID
126699592 12669959 2 SS BYETTA EXENATIDE 1 Subcutaneous U U 21773 5 UG SOLUTION FOR INJECTION IN PRE-FILLED PEN BID
126699592 12669959 3 SS BYETTA EXENATIDE 1 Subcutaneous U U 21773 10 UG SOLUTION FOR INJECTION IN PRE-FILLED PEN BID
126699592 12669959 4 SS BYETTA EXENATIDE 1 Subcutaneous U U 21773 10 UG SOLUTION FOR INJECTION IN PRE-FILLED PEN BID
126699592 12669959 5 SS BYETTA EXENATIDE 1 Subcutaneous U U 21773 10 UG SOLUTION FOR INJECTION IN PRE-FILLED PEN BID

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
126699592 12669959 1 Diabetes mellitus
126699592 12669959 2 Diabetes mellitus
126699592 12669959 3 Diabetes mellitus
126699592 12669959 4 Diabetes mellitus
126699592 12669959 5 Diabetes mellitus

Outcome of event

Event ID CASEID OUTC COD
126699592 12669959 HO

Reactions reported

Event ID CASEID DRUG REC ACT PT
126699592 12669959 Abdominal discomfort
126699592 12669959 Abdominal pain upper
126699592 12669959 Blood glucose fluctuation
126699592 12669959 Chronic gastritis
126699592 12669959 Constipation
126699592 12669959 Dizziness
126699592 12669959 Drug ineffective
126699592 12669959 Dyspepsia
126699592 12669959 Eructation
126699592 12669959 Gastrooesophageal reflux disease
126699592 12669959 Generalised erythema
126699592 12669959 Headache
126699592 12669959 Hypoglycaemia
126699592 12669959 Intentional product misuse
126699592 12669959 Nausea
126699592 12669959 Night sweats
126699592 12669959 Palpitations
126699592 12669959 Somnolence
126699592 12669959 Vomiting

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
126699592 12669959 1 2013 0
126699592 12669959 2 20150629 0
126699592 12669959 3 201505 0
126699592 12669959 4 201504 0
126699592 12669959 5 20150730 0