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
127903861 12790386 1 I 201409 20141116 20160928 20160928 PER US-ASTRAZENECA-2014SE88996 ASTRAZENECA 27908.00 DY F Y 86.20000 KG 20160929 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
127903861 12790386 1 PS BYDUREON EXENATIDE 1 Subcutaneous AAA1068 22200 2 MG /wk
127903861 12790386 2 SS BYETTA EXENATIDE 1 Unknown N U 0 SOLUTION FOR INJECTION IN PRE-FILLED PEN
127903861 12790386 3 C GLIPIZIDE. GLIPIZIDE 1 Unknown 0
127903861 12790386 4 C METFORMIN METFORMIN HYDROCHLORIDE 1 Unknown 0
127903861 12790386 5 C LEVEMIR INSULIN DETEMIR 1 Unknown 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
127903861 12790386 1 Type 2 diabetes mellitus
127903861 12790386 2 Type 2 diabetes mellitus
127903861 12790386 3 Type 2 diabetes mellitus
127903861 12790386 4 Type 2 diabetes mellitus
127903861 12790386 5 Type 2 diabetes mellitus

Outcome of event

no results found

Reactions reported

Event ID CASEID DRUG REC ACT PT
127903861 12790386 Arthritis
127903861 12790386 Blood glucose decreased
127903861 12790386 Feeling abnormal
127903861 12790386 Incorrect dose administered
127903861 12790386 Injection site extravasation
127903861 12790386 Injection site haemorrhage
127903861 12790386 Nausea
127903861 12790386 Underdose
127903861 12790386 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
127903861 12790386 1 201409 0