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
126945892 12694589 2 F 20160720 20160830 20160829 20160907 EXP CN-ASTRAZENECA-2016SE89179 ASTRAZENECA 0.00 F Y 0.00000 20160907 MD 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
126945892 12694589 1 PS BYETTA EXENATIDE 1 Unknown 60 UG U 21773 5 UG SOLUTION FOR INJECTION IN PRE-FILLED PEN BID
126945892 12694589 2 SS BYETTA EXENATIDE 1 Unknown 60 UG U 21773 5 UG SOLUTION FOR INJECTION IN PRE-FILLED PEN BID

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
126945892 12694589 1 Diabetes mellitus
126945892 12694589 2 Obesity

Outcome of event

Event ID CASEID OUTC COD
126945892 12694589 HO

Reactions reported

Event ID CASEID DRUG REC ACT PT
126945892 12694589 Hyperparathyroidism
126945892 12694589 Off label use
126945892 12694589 Parathyroid cyst
126945892 12694589 Product use issue
126945892 12694589 Reflux gastritis
126945892 12694589 Vomiting
126945892 12694589 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
126945892 12694589 1 20160720 20160725 0
126945892 12694589 2 20160720 20160725 0