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
127904351 12790435 1 I 2005 20080923 20160929 20160929 PER US-ASTRAZENECA-2008BM13590 ASTRAZENECA 54.00 YR F Y 86.20000 KG 20160929 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
127904351 12790435 1 PS BYETTA EXENATIDE 1 Subcutaneous U 21773 5 UG SOLUTION FOR INJECTION IN PRE-FILLED PEN BID
127904351 12790435 2 SS BYETTA EXENATIDE 1 Subcutaneous U 21773 10 UG SOLUTION FOR INJECTION IN PRE-FILLED PEN BID
127904351 12790435 3 SS BYETTA EXENATIDE 1 Subcutaneous U A404197 21773 5 UG SOLUTION FOR INJECTION IN PRE-FILLED PEN BID
127904351 12790435 4 SS BYETTA EXENATIDE 1 Subcutaneous U A533578A 21773 5 UG SOLUTION FOR INJECTION IN PRE-FILLED PEN BID
127904351 12790435 5 SS BYDUREON EXENATIDE 1 Subcutaneous 0 2 MG /wk
127904351 12790435 6 SS LISINOPRIL. LISINOPRIL 1 Oral EITHER 20 MG OR 2.5 MG, DAILY 0 TABLET
127904351 12790435 7 C GLYBURIDE. GLYBURIDE 1 UNK 0
127904351 12790435 8 C GLUCOPHAGE /USA/ 2 UNK 0
127904351 12790435 9 C METFORMIN METFORMIN HYDROCHLORIDE 1 Oral 0 4 DF QD
127904351 12790435 10 C GLIPIZIDE. GLIPIZIDE 1 Oral 0 2 DF QD
127904351 12790435 11 C LEXAPRO ESCITALOPRAM OXALATE 1 Oral 0 20 MG QD
127904351 12790435 12 C LEXAPRO ESCITALOPRAM OXALATE 1 Oral 0 20 MG QD
127904351 12790435 13 C LIPITOR ATORVASTATIN CALCIUM 1 Oral EITHER 20 MG THE OTHER IS 2.5 MG,DAILY 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
127904351 12790435 1 Type 2 diabetes mellitus
127904351 12790435 2 Type 2 diabetes mellitus
127904351 12790435 3 Type 2 diabetes mellitus
127904351 12790435 4 Type 2 diabetes mellitus
127904351 12790435 5 Type 2 diabetes mellitus
127904351 12790435 6 Hypertension
127904351 12790435 7 Type 2 diabetes mellitus
127904351 12790435 8 Type 2 diabetes mellitus
127904351 12790435 9 Type 2 diabetes mellitus
127904351 12790435 10 Type 2 diabetes mellitus
127904351 12790435 11 Depression
127904351 12790435 12 Ill-defined disorder
127904351 12790435 13 Blood cholesterol increased

Outcome of event

no results found

Reactions reported

Event ID CASEID DRUG REC ACT PT
127904351 12790435 Blood glucose decreased
127904351 12790435 Blood glucose increased
127904351 12790435 Headache
127904351 12790435 Hypotension
127904351 12790435 Injection site haemorrhage
127904351 12790435 Injection site pain
127904351 12790435 Intentional product misuse
127904351 12790435 Malaise
127904351 12790435 Memory impairment
127904351 12790435 Nausea
127904351 12790435 Tremor
127904351 12790435 Urinary tract infection
127904351 12790435 Vomiting
127904351 12790435 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
127904351 12790435 1 2005 2005 0
127904351 12790435 2 2005 2005 0
127904351 12790435 3 2005 0
127904351 12790435 4 2009 0
127904351 12790435 5 2016 0
127904351 12790435 10 201601 0