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
124568373 12456837 3 F 20160213 20160712 20160610 20160720 EXP RO-KADMON PHARMACEUTICALS, LLC-KAD201606-002124 KADMON 73.43 YR M Y 65.00000 KG 20160720 MD 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
124568373 12456837 1 PS RIBAVIRIN. RIBAVIRIN 1 Oral FILM-COATED TABLET Y 77456 FILM-COATED TABLET
124568373 12456837 2 SS RIBAVIRIN. RIBAVIRIN 1 Oral Y 77456 800 MG
124568373 12456837 3 SS RIBAVIRIN. RIBAVIRIN 1 Oral Y 77456 1000 MG
124568373 12456837 4 SS RIBAVIRIN. RIBAVIRIN 1 Oral Y 77456 800 MG
124568373 12456837 5 SS RIBAVIRIN. RIBAVIRIN 1 Oral Y 77456 1000 MG
124568373 12456837 6 SS Viekirax OMBITASVIRPARITAPREVIRRITONAVIR 1 Oral FILM-COATED TABLET 0 FILM-COATED TABLET
124568373 12456837 7 SS Viekirax OMBITASVIRPARITAPREVIRRITONAVIR 1 0
124568373 12456837 8 SS Exviera DASABUVIR 1 Oral FILM-COATED TABLET 0 FILM-COATED TABLET
124568373 12456837 9 SS Exviera DASABUVIR 1 0
124568373 12456837 10 C SOTALOL. SOTALOL 1 Oral 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
124568373 12456837 1 Hepatitis C
124568373 12456837 2 Hepatic cirrhosis
124568373 12456837 6 Hepatitis C
124568373 12456837 7 Hepatic cirrhosis
124568373 12456837 8 Hepatitis C
124568373 12456837 9 Hepatic cirrhosis
124568373 12456837 10 Cardiac disorder

Outcome of event

Event ID CASEID OUTC COD
124568373 12456837 HO

Reactions reported

Event ID CASEID DRUG REC ACT PT
124568373 12456837 Abdominal pain
124568373 12456837 Atrial fibrillation
124568373 12456837 Burn oesophageal
124568373 12456837 Diarrhoea
124568373 12456837 Headache
124568373 12456837 Jaundice
124568373 12456837 Malaise
124568373 12456837 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
124568373 12456837 1 20160213 20160221 0
124568373 12456837 2 20160224 20160227 0
124568373 12456837 3 20160228 20160422 0
124568373 12456837 4 20160426 20160430 0
124568373 12456837 5 20160501 20160507 0
124568373 12456837 6 20160213 20160507 0
124568373 12456837 8 20160213 20160507 0
124568373 12456837 10 20151101 0