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
125904401 12590440 1 I 20090415 20090416 20160725 20160725 PER US-ASTRAZENECA-2009BM04976 ASTRAZENECA 16905.00 DY F Y 58.50000 KG 20160726 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
125904401 12590440 1 PS BYETTA EXENATIDE 1 Subcutaneous Y A524229A 21773 5 UG SOLUTION FOR INJECTION IN PRE-FILLED PEN BID
125904401 12590440 2 SS BYETTA EXENATIDE 1 Subcutaneous Y 21773 5 UG SOLUTION FOR INJECTION IN PRE-FILLED PEN BID
125904401 12590440 3 SS BYDUREON EXENATIDE 1 Subcutaneous 0 2 MG /wk
125904401 12590440 4 C METFORMIN METFORMIN HYDROCHLORIDE 1 0
125904401 12590440 5 C OTHER MEDICATION UNSPECIFIED INGREDIENT 1 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
125904401 12590440 1 Type 2 diabetes mellitus
125904401 12590440 2 Type 2 diabetes mellitus
125904401 12590440 3 Type 2 diabetes mellitus

Outcome of event

no results found

Reactions reported

Event ID CASEID DRUG REC ACT PT
125904401 12590440 Drug ineffective
125904401 12590440 Injection site nodule
125904401 12590440 Injection site pain
125904401 12590440 Nausea
125904401 12590440 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
125904401 12590440 1 20090407 0
125904401 12590440 2 201403 20151212 0
125904401 12590440 3 20160107 0