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
125063693 12506369 3 F 20160205 20160902 20160628 20160906 EXP RO-ABBVIE-16P-135-1555854-00 ABBVIE 60.79 YR M Y 0.00000 20160906 MD COUNTRY NOT SPECIFIED 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
125063693 12506369 1 PS VIEKIRAX OMBITASVIRPARITAPREVIRRITONAVIR 1 Oral 2 TABL/DAY IN THE MORNING 506408D 206619
125063693 12506369 2 SS VIEKIRAX OMBITASVIRPARITAPREVIRRITONAVIR 1 506408D 206619
125063693 12506369 3 SS EXVIERA DASABUVIR 1 Oral 2*1 TABL/DAY 506828D 206619
125063693 12506369 4 SS EXVIERA DASABUVIR 1 506828D 206619
125063693 12506369 5 SS REBETOL RIBAVIRIN 1 Oral Y 0
125063693 12506369 6 SS REBETOL RIBAVIRIN 1 Oral Y 0
125063693 12506369 7 C BETALOK ZOK 2 Oral 0
125063693 12506369 8 C ATACAND CANDESARTAN CILEXETIL 1 Oral 0
125063693 12506369 9 C NOVORAPID INSULIN 2 Subcutaneous 10 IU AT 13.00, NOON 0
125063693 12506369 10 C LEVEMIR INSULIN DETEMIR 1 Subcutaneous 10 IU AT 18.30, EVENING 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
125063693 12506369 1 Hepatitis C
125063693 12506369 2 Hepatic cirrhosis
125063693 12506369 3 Hepatic cirrhosis
125063693 12506369 4 Hepatitis C
125063693 12506369 5 Hepatitis C
125063693 12506369 6 Hepatic cirrhosis
125063693 12506369 7 Hypertension
125063693 12506369 8 Hypertension
125063693 12506369 9 Type 2 diabetes mellitus
125063693 12506369 10 Type 2 diabetes mellitus

Outcome of event

Event ID CASEID OUTC COD
125063693 12506369 HO
125063693 12506369 DE

Reactions reported

Event ID CASEID DRUG REC ACT PT
125063693 12506369 Anaemia
125063693 12506369 Cardio-respiratory arrest
125063693 12506369 Haemorrhagic stroke
125063693 12506369 Hepatic failure

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
125063693 12506369 1 20160111 20160403 0
125063693 12506369 3 20160111 20160403 0
125063693 12506369 5 20160111 0
125063693 12506369 6 20160403 0
125063693 12506369 7 2010 0
125063693 12506369 8 2015 0
125063693 12506369 9 201501 0
125063693 12506369 10 201501 0