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
125231821 12523182 1 I 20160516 20160702 20160702 PER US-ASTRAZENECA-2016SE53615 ASTRAZENECA 0.00 F Y 113.40000 KG 20160702 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
125231821 12523182 1 PS BYETTA EXENATIDE 1 Unknown 250 MCG / 2.4 ML PEN, 10 UG, TWO TIMES A DAY 21773 SOLUTION FOR INJECTION IN PRE-FILLED PEN
125231821 12523182 2 SS BYETTA EXENATIDE 1 Unknown 250 MCG / 2.4 ML PEN, 10 UG, TWO TIMES A DAY 21773 SOLUTION FOR INJECTION IN PRE-FILLED PEN
125231821 12523182 3 C JENTADUETO LINAGLIPTINMETFORMIN HYDROCHLORIDE 1 0 2.5 MG BID
125231821 12523182 4 C SYNTHROID LEVOTHYROXINE SODIUM 1 0
125231821 12523182 5 C BYSTOLIC NEBIVOLOL HYDROCHLORIDE 1 10.0MG UNKNOWN 0 10 MG

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
125231821 12523182 3 Blood glucose decreased
125231821 12523182 4 Thyroid disorder

Outcome of event

no results found

Reactions reported

Event ID CASEID DRUG REC ACT PT
125231821 12523182 Arrhythmia
125231821 12523182 Blood glucose increased
125231821 12523182 Blood pressure increased
125231821 12523182 Glycosylated haemoglobin increased
125231821 12523182 Off label use
125231821 12523182 Product contamination physical
125231821 12523182 Weight increased

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
125231821 12523182 1 2012 0
125231821 12523182 2 201602 0
125231821 12523182 4 2006 0
125231821 12523182 5 2015 0