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
126965311 12696531 1 I 20160823 20160830 20160830 PER US-ASTRAZENECA-2016SE91349 ASTRAZENECA 0.00 F Y 55.80000 KG 20160830 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
126965311 12696531 1 PS SYMLIN PRAMLINTIDE ACETATE 1 Subcutaneous 273960 UG U U 21332 60 UG INJECTION TID
126965311 12696531 2 C LANTUS INSULIN GLARGINE 1 Subcutaneous 0 22 IU/KG QD
126965311 12696531 3 C NOVOLOG INSULIN ASPART 1 Subcutaneous 10 UNITS DOSAGE SPACED THROUGHOUT THE DAY BEFORE BREAKFAST,LUNCH, DINNER UNKNOWN 0
126965311 12696531 4 C JARDIANCE EMPAGLIFLOZIN 1 Oral UNKNOWN 0 QD

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
126965311 12696531 1 Type 1 diabetes mellitus
126965311 12696531 2 Type 1 diabetes mellitus
126965311 12696531 3 Type 1 diabetes mellitus
126965311 12696531 4 Type 1 diabetes mellitus

Outcome of event

no results found

Reactions reported

Event ID CASEID DRUG REC ACT PT
126965311 12696531 Weight decreased
126965311 12696531 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
126965311 12696531 1 201204 201606 0
126965311 12696531 4 201605 0