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
127193291 12719329 1 I 20160516 20160516 20160907 20160907 PER US-ASTRAZENECA-2016SE53343 ASTRAZENECA 24908.00 DY F Y 59.00000 KG 20160907 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
127193291 12719329 1 PS BYETTA EXENATIDE 1 Subcutaneous 5.0UG UNKNOWN U 0 5 UG SOLUTION FOR INJECTION IN PRE-FILLED PEN
127193291 12719329 2 SS BYETTA EXENATIDE 1 Subcutaneous 10.0UG UNKNOWN U 0 10 UG SOLUTION FOR INJECTION IN PRE-FILLED PEN
127193291 12719329 3 SS BYETTA EXENATIDE 1 Subcutaneous 10.0UG UNKNOWN U 0 10 UG SOLUTION FOR INJECTION IN PRE-FILLED PEN BID
127193291 12719329 4 SS PRILOSEC OMEPRAZOLE MAGNESIUM 1 Oral U 0 MODIFIED-RELEASE TABLET

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
127193291 12719329 1 Diabetes mellitus
127193291 12719329 2 Diabetes mellitus
127193291 12719329 3 Diabetes mellitus
127193291 12719329 4 Nausea

Outcome of event

no results found

Reactions reported

Event ID CASEID DRUG REC ACT PT
127193291 12719329 Basedow's disease
127193291 12719329 Circumstance or information capable of leading to medication error
127193291 12719329 Feeding disorder
127193291 12719329 Migraine
127193291 12719329 Nausea
127193291 12719329 Vomiting

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
127193291 12719329 3 20160516 0