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
125617741 12561774 1 I 2016 20160706 20160715 20160715 EXP US-NOVOPROD-500467 NOVO NORDISK 66.00 YR E F Y 86.17000 KG 20160715 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
125617741 12561774 1 PS VICTOZA LIRAGLUTIDE 1 Subcutaneous 0.6 MG, QD Y FS6W970 22341 .6 MG SOLUTION FOR INJECTION QD
125617741 12561774 2 SS VICTOZA LIRAGLUTIDE 1 Subcutaneous 1.2 MG, QD Y FS6W970 22341 1.2 MG SOLUTION FOR INJECTION QD
125617741 12561774 3 SS VICTOZA LIRAGLUTIDE 1 Subcutaneous 0.6 MG, QD Y FS6W970 22341 .6 MG SOLUTION FOR INJECTION QD
125617741 12561774 4 C LEVOTHYROXINE. LEVOTHYROXINE 1 75 ?G, QD 0 75 UG QD

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
125617741 12561774 1 Type 2 diabetes mellitus
125617741 12561774 4 Hypothyroidism

Outcome of event

Event ID CASEID OUTC COD
125617741 12561774 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
125617741 12561774 Abdominal pain upper
125617741 12561774 Asthma
125617741 12561774 Diarrhoea
125617741 12561774 Dyspepsia
125617741 12561774 Headache
125617741 12561774 Nausea
125617741 12561774 Off label use
125617741 12561774 Upper respiratory tract infection

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
125617741 12561774 1 201604 2016 0
125617741 12561774 2 2016 0
125617741 12561774 3 2016 20160706 0