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
126857501 12685750 1 I 2016 20160115 20160825 20160825 PER US-NOVOPROD-477841 NOVO NORDISK 46.00 YR A F Y 0.00000 20160825 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
126857501 12685750 1 PS VICTOZA LIRAGLUTIDE 1 Subcutaneous 0.6 MG, QD Y UNKNOWN 22341 .6 MG SOLUTION FOR INJECTION QD
126857501 12685750 2 SS VICTOZA LIRAGLUTIDE 1 Subcutaneous 0.6 MG, QOD Y UNKNOWN 22341 .6 MG SOLUTION FOR INJECTION QOD
126857501 12685750 3 C GLUCOPHAGE METFORMIN HYDROCHLORIDE 1 Subcutaneous UNKNOWN 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
126857501 12685750 1 Type 2 diabetes mellitus
126857501 12685750 3 Type 2 diabetes mellitus

Outcome of event

no results found

Reactions reported

Event ID CASEID DRUG REC ACT PT
126857501 12685750 Dizziness
126857501 12685750 Headache
126857501 12685750 Insomnia
126857501 12685750 Nausea
126857501 12685750 Off label use
126857501 12685750 Pyrexia
126857501 12685750 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
126857501 12685750 1 20160111 2016 0
126857501 12685750 2 2016 0