The Safety Rates Drug Report

Member Login
2004.Q1    2004.Q2    2004.Q3    2004.Q4    2005.Q1    2005.Q2    2005.Q3    2005.Q4    2006.Q1    2006.Q2    2006.Q3    2006.Q4    2007.Q1    2007.Q2    2007.Q3    2007.Q4    2008.Q1    2008.Q2    2008.Q3    2008.Q4    2009.Q1    2009.Q2    2009.Q3    2009.Q4    2010.Q1    2010.Q2    2010.Q3    2010.Q4    2011.Q1    2011.Q2    2011.Q3    2011.Q4    2012.Q1    2012.Q2    2012.Q3    2012.Q4    2013.Q1    2013.Q2    2013.Q3    2013.Q4    2014.Q1    2014.Q2    2014.Q3    2014.Q4    2015.Q1    2015.Q2    2015.Q3    2015.Q4    2016.Q1    2016.Q2    2016.Q3   

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
126866241 12686624 1 I 20150930 20150930 20160825 20160825 PER US-NOVOPROD-466482 NOVO NORDISK 59.00 YR A M 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
126866241 12686624 1 PS VICTOZA LIRAGLUTIDE 1 Subcutaneous 1.8 MG, QD ES6P735 22341 1.8 MG SOLUTION FOR INJECTION QD
126866241 12686624 2 SS VICTOZA LIRAGLUTIDE 1 0.6 MG, QD ES6P735 22341 .6 MG SOLUTION FOR INJECTION QD
126866241 12686624 3 SS RIBAVIRIN. RIBAVIRIN 1 Oral UNK U U UNKNOWN 0
126866241 12686624 4 SS HARVONI LEDIPASVIRSOFOSBUVIR 1 Oral UNK U U UNKNOWN 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
126866241 12686624 1 Type 2 diabetes mellitus
126866241 12686624 3 Hepatitis C
126866241 12686624 4 Hepatitis C

Outcome of event

no results found

Reactions reported

Event ID CASEID DRUG REC ACT PT
126866241 12686624 Back pain
126866241 12686624 Blood glucose increased
126866241 12686624 Diarrhoea
126866241 12686624 Dyspepsia
126866241 12686624 Headache
126866241 12686624 Hyperhidrosis
126866241 12686624 Incorrect dose administered
126866241 12686624 Insomnia
126866241 12686624 Miliaria
126866241 12686624 Nausea
126866241 12686624 Product label confusion
126866241 12686624 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
126866241 12686624 1 20150930 0
126866241 12686624 2 20151001 0