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
127696911 12769691 1 I 20160919 20160922 20160922 EXP RO-ROCHE-1832333 ROCHE SUCEVEANU A, MAZILU L, ARAMA V, SUCEVEANU A, PAREPA I, CENUSA A, CATINEAN A, CRACIUN L AND VOINEA F. MAJOR DRIVERS INFLUENCING ADHERENCE AND QUALITY OF LIFE DURING ANTIVIRAL TRIPLE THERAPY IN PATIENTS WITH CHRONIC HEPATITIS C . ARS MEDICA TOMITANA 2016 MAY 01;22 (2):83-91. 0.00 Y 0.00000 20160922 OT RO RO

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
127696911 12769691 1 PS RIBAVIRIN. RIBAVIRIN 1 Unknown U 21511
127696911 12769691 2 SS RIBAVIRIN. RIBAVIRIN 1 U 21511
127696911 12769691 3 SS Peg-Interferon Alfa 2a PEGINTERFERON ALFA-2A 1 Unknown U 103964
127696911 12769691 4 SS Peg-Interferon Alfa 2a PEGINTERFERON ALFA-2A 1 U 103964
127696911 12769691 5 SS PEGINTERFERON ALFA-2B PEGINTERFERON ALFA-2B 1 Unknown U 0
127696911 12769691 6 SS PEGINTERFERON ALFA-2B PEGINTERFERON ALFA-2B 1 U 0
127696911 12769691 7 I TELAPREVIR TELAPREVIR 1 Unknown U 0
127696911 12769691 8 I TELAPREVIR TELAPREVIR 1 U 0
127696911 12769691 9 SS BOCEPREVIR BOCEPREVIR 1 Unknown U 0
127696911 12769691 10 SS BOCEPREVIR BOCEPREVIR 1 U 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
127696911 12769691 1 Chronic hepatitis C
127696911 12769691 2 Hepatic cirrhosis
127696911 12769691 3 Chronic hepatitis C
127696911 12769691 4 Hepatic cirrhosis
127696911 12769691 5 Chronic hepatitis C
127696911 12769691 6 Hepatic cirrhosis
127696911 12769691 7 Chronic hepatitis C
127696911 12769691 8 Hepatic cirrhosis
127696911 12769691 9 Chronic hepatitis C
127696911 12769691 10 Hepatic cirrhosis

Outcome of event

Event ID CASEID OUTC COD
127696911 12769691 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
127696911 12769691 Anaemia
127696911 12769691 Chills
127696911 12769691 Diarrhoea
127696911 12769691 Drug interaction
127696911 12769691 Dysgeusia
127696911 12769691 Fatigue
127696911 12769691 Gastrointestinal disorder
127696911 12769691 General physical health deterioration
127696911 12769691 Influenza like illness
127696911 12769691 Insomnia
127696911 12769691 Irritability
127696911 12769691 Leukopenia
127696911 12769691 Nausea
127696911 12769691 Neutropenia
127696911 12769691 Pruritus
127696911 12769691 Rash
127696911 12769691 Thrombocytopenia
127696911 12769691 Vomiting
127696911 12769691 Weight decreased

Reporting Sources (this data is often not reported and may therefore be missing here)

no results found

Therapies reported

no results found