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
126168542 12616854 2 F 2013 20160809 20160802 20160917 PER US-ASTRAZENECA-2016SE72835 ASTRAZENECA 60.00 YR F Y 74.80000 KG 20160917 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
126168542 12616854 1 PS BYETTA EXENATIDE 1 Subcutaneous U 21773 5 UG SOLUTION FOR INJECTION IN PRE-FILLED PEN BID
126168542 12616854 2 SS BYETTA EXENATIDE 1 Subcutaneous U 21773 10 UG SOLUTION FOR INJECTION IN PRE-FILLED PEN BID
126168542 12616854 3 SS BYDUREON EXENATIDE 1 Subcutaneous FN0139 22200 2 MG /wk
126168542 12616854 4 C METFORMIN METFORMIN HYDROCHLORIDE 1 Oral 0 1000 MG BID

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
126168542 12616854 1 Type 2 diabetes mellitus
126168542 12616854 2 Type 2 diabetes mellitus
126168542 12616854 3 Type 2 diabetes mellitus
126168542 12616854 4 Type 2 diabetes mellitus

Outcome of event

no results found

Reactions reported

Event ID CASEID DRUG REC ACT PT
126168542 12616854 Decreased appetite
126168542 12616854 Device leakage
126168542 12616854 Malaise

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
126168542 12616854 1 2013 0
126168542 12616854 2 2014 20160701 0
126168542 12616854 3 20160702 0