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
127668261 12766826 1 I 2013 20160912 20160921 20160921 EXP US-NOVOPROD-510708 NOVO NORDISK 52.00 YR A F Y 0.00000 20160921 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
127668261 12766826 1 PS LEVEMIR INSULIN DETEMIR 1 Subcutaneous UNKNOWN EZF0589 21536 SOLUTION FOR INJECTION
127668261 12766826 2 SS NOVOLOG INSULIN ASPART 1 Subcutaneous UNKNOWN EZF0509 0 SOLUTION FOR INJECTION
127668261 12766826 3 SS LANTUS INSULIN GLARGINE 1 Subcutaneous UNKNOWN U U UNKNOWN 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
127668261 12766826 1 Type 2 diabetes mellitus
127668261 12766826 2 Type 2 diabetes mellitus
127668261 12766826 3 Type 2 diabetes mellitus

Outcome of event

Event ID CASEID OUTC COD
127668261 12766826 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
127668261 12766826 Blood glucose increased
127668261 12766826 Glycosylated haemoglobin increased
127668261 12766826 Organ failure

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
127668261 12766826 1 2013 0
127668261 12766826 2 2012 0
127668261 12766826 3 2013 0