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
126855431 12685543 1 I 20150730 20150803 20160825 20160825 PER US-NOVOPROD-459222 NOVO NORDISK 47.00 YR A F Y 0.00000 20160825 MD 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
126855431 12685543 1 PS VICTOZA LIRAGLUTIDE 1 Subcutaneous 0.6 MG, QD (DOSE TAKEN IN THE MORNING) Y Y UNKNOWN 22341 .6 MG SOLUTION FOR INJECTION QD
126855431 12685543 2 SS VICTOZA LIRAGLUTIDE 1 Subcutaneous 0.6 MG, QD (DOSE TAKEN IN THE MID AFTERNOON) Y Y UNKNOWN 22341 .6 MG SOLUTION FOR INJECTION QD

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
126855431 12685543 1 Type 2 diabetes mellitus

Outcome of event

no results found

Reactions reported

Event ID CASEID DRUG REC ACT PT
126855431 12685543 Decreased appetite
126855431 12685543 Headache
126855431 12685543 Nausea
126855431 12685543 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
126855431 12685543 1 20150730 20150731 0
126855431 12685543 2 20150802 0