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
126603122 12660312 2 F 201201 20160916 20160817 20160922 EXP US-ASTRAZENECA-2010BM06379 ASTRAZENECA 642.00 MON F Y 120.20000 KG 20160922 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
126603122 12660312 1 PS BYETTA EXENATIDE 1 Subcutaneous A678711A 21773 5 UG SOLUTION FOR INJECTION IN PRE-FILLED PEN BID
126603122 12660312 2 SS BYDUREON EXENATIDE 1 Subcutaneous FT0082 0 2 MG /wk
126603122 12660312 3 C EXENATIDE EXENATIDE 1 0 SOLUTION FOR INJECTION
126603122 12660312 4 C GLUCOPHAGE METFORMIN HYDROCHLORIDE 1 UNK 0
126603122 12660312 5 C TUMS CALCIUM CARBONATE 1 0
126603122 12660312 6 C NEURONTIN GABAPENTIN 1 Oral POSSIBLE 200MG, TWICE A DAY 0
126603122 12660312 7 C NEURONTIN GABAPENTIN 1 Oral POSSIBLE 200MG, TWICE A DAY 0
126603122 12660312 8 C NOVOLOG INSULIN ASPART 1 Subcutaneous 7 UNITS OVER 450 0
126603122 12660312 9 C LEVEMIR INSULIN DETEMIR 1 Subcutaneous 46 UNITS IN THE AM AND 40 UNITS IN THE PM 0
126603122 12660312 10 C VITAMINS VITAMINS 1 0
126603122 12660312 11 C INSULIN INSULIN NOS 1 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
126603122 12660312 1 Type 2 diabetes mellitus
126603122 12660312 2 Type 2 diabetes mellitus
126603122 12660312 5 Nausea
126603122 12660312 6 Neuropathy peripheral
126603122 12660312 7 Pain
126603122 12660312 8 Type 2 diabetes mellitus
126603122 12660312 9 Type 2 diabetes mellitus

Outcome of event

Event ID CASEID OUTC COD
126603122 12660312 HO

Reactions reported

Event ID CASEID DRUG REC ACT PT
126603122 12660312 Abdominal mass
126603122 12660312 Glycosylated haemoglobin increased
126603122 12660312 Intentional product misuse
126603122 12660312 Localised infection
126603122 12660312 Lymphoedema
126603122 12660312 Nausea
126603122 12660312 Needle issue
126603122 12660312 Neuropathy peripheral
126603122 12660312 Pain in extremity
126603122 12660312 Peripheral swelling
126603122 12660312 Sepsis

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
126603122 12660312 1 20100428 0
126603122 12660312 6 2016 0
126603122 12660312 7 2016 0