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
121509552 12150955 2 F 2012 20160425 20160304 20160909 PER US-ASTRAZENECA-2012BM06276 ASTRAZENECA 70.00 YR F Y 81.20000 KG 20160909 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
121509552 12150955 1 PS BYETTA EXENATIDE 1 Subcutaneous 21773 5 UG SOLUTION FOR INJECTION IN PRE-FILLED PEN BID
121509552 12150955 2 SS BYETTA EXENATIDE 1 Subcutaneous A869551A 21773 10 UG SOLUTION FOR INJECTION IN PRE-FILLED PEN BID
121509552 12150955 3 SS BYETTA EXENATIDE 1 Subcutaneous 21773 10 UG SOLUTION FOR INJECTION IN PRE-FILLED PEN BID
121509552 12150955 4 C GLUCOPHAGE METFORMIN HYDROCHLORIDE 1 Oral EVERY DAY 0
121509552 12150955 5 C GLIPIZIDE. GLIPIZIDE 1 Oral 0 10 MG QD
121509552 12150955 6 C SYNTHROID LEVOTHYROXINE SODIUM 1 Oral 0 30 UG
121509552 12150955 7 C NEURONTIN GABAPENTIN 1 Oral 0 100 MG QD
121509552 12150955 8 C PAROXETINE HCL PAROXETINE HYDROCHLORIDE 1 Oral 0 30 MG QD
121509552 12150955 9 C TRAZODONE TRAZODONE HYDROCHLORIDE 1 Oral 0 150 MG QD

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
121509552 12150955 1 Type 2 diabetes mellitus
121509552 12150955 2 Type 2 diabetes mellitus
121509552 12150955 3 Type 2 diabetes mellitus
121509552 12150955 4 Type 2 diabetes mellitus
121509552 12150955 5 Type 2 diabetes mellitus
121509552 12150955 7 Feeling abnormal
121509552 12150955 8 Depression
121509552 12150955 9 Depression

Outcome of event

no results found

Reactions reported

Event ID CASEID DRUG REC ACT PT
121509552 12150955 Asthenopia
121509552 12150955 Bronchitis
121509552 12150955 Dry mouth
121509552 12150955 Injection site pain
121509552 12150955 Injection site pruritus
121509552 12150955 Injection site urticaria
121509552 12150955 Product quality issue
121509552 12150955 Underdose
121509552 12150955 Urine output increased
121509552 12150955 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
121509552 12150955 3 20160118 0