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
126577871 12657787 1 I 20160802 20160817 20160817 PER US-ASTRAZENECA-2016SE84715 ASTRAZENECA 0.00 F Y 87.10000 KG 20160817 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
126577871 12657787 1 PS BYDUREON EXENATIDE 1 Subcutaneous U 22200 2 MG /wk
126577871 12657787 2 SS BYETTA EXENATIDE 1 Subcutaneous TWICE A DAY U NOT REPORTED 0 SOLUTION FOR INJECTION IN PRE-FILLED PEN
126577871 12657787 3 C HIGH BLOOD PRESSURE MEDIACTION 2 0
126577871 12657787 4 C SOMETHING FOR CHOLESTEROL 2 0
126577871 12657787 5 C ALLERGY MEDICATION DIPHENHYDRAMINE HYDROCHLORIDE 1 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
126577871 12657787 1 Diabetes mellitus
126577871 12657787 2 Diabetes mellitus

Outcome of event

no results found

Reactions reported

Event ID CASEID DRUG REC ACT PT
126577871 12657787 Injection site bruising
126577871 12657787 Injection site extravasation
126577871 12657787 Injection site haemorrhage
126577871 12657787 Injection site pain

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

no results found

Therapies reported

no results found