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
126677761 12667776 1 I 20160813 20160819 20160819 EXP US-ASTRAZENECA-2016SE88158 ASTRAZENECA 0.00 F Y 75.30000 KG 20160819 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
126677761 12667776 1 PS BYETTA EXENATIDE 1 Subcutaneous 10MCG TWICE A DAY, BEFORE HER MORNING AND EVENING MEAL U AZ160018 21773 SOLUTION FOR INJECTION IN PRE-FILLED PEN
126677761 12667776 2 C GLUCOPHAGE METFORMIN HYDROCHLORIDE 1 Oral GENERIC 0
126677761 12667776 3 C GLIMEPRIDE GLIMEPIRIDE 1 Oral 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
126677761 12667776 1 Diabetes mellitus
126677761 12667776 2 Diabetes mellitus
126677761 12667776 3 Diabetes mellitus

Outcome of event

Event ID CASEID OUTC COD
126677761 12667776 HO

Reactions reported

Event ID CASEID DRUG REC ACT PT
126677761 12667776 Blood pressure increased
126677761 12667776 Cardiac disorder
126677761 12667776 Decreased appetite
126677761 12667776 Device leakage
126677761 12667776 Feeling abnormal
126677761 12667776 Weight decreased

Reporting Sources (this data is often not reported and may therefore be missing here)

no results found

Therapies reported

no results found