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
127156191 12715619 1 I 20160421 20160906 20160906 EXP US-MLMSERVICE-20160818-0386343-1 US-ACCORD-043753 ACCORD PATEL SJ, KUTEN SA, MUSICK WL, GABER AO, MONSOUR HP, KNIGHT RJ. COMBINATION DRUG PRODUCTS FOR HIV-A WORD OF CAUTION FOR THE TRANSPLANT CLINICIAN.AMERICAN JOURNAL OF TRANSPLANTATION. 2016; 16(8):2479-2482 38.00 YR M Y 0.00000 20160906 OT 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
127156191 12715619 1 PS TACROLIMUS. TACROLIMUS 1 STABLE DOSE Y 91195 3 MG Q12H
127156191 12715619 2 I STRIBILD COBICISTATELVITEGRAVIREMTRICITABINETENOFOVIR DISOPROXIL FUMARATE 1 Y 0 1 DF TABLET
127156191 12715619 3 C PREDNISONE. PREDNISONE 1 0 7.5 MG
127156191 12715619 4 C MYCOPHENOLIC ACID. MYCOPHENOLIC ACID 1 0 360 MG BID

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
127156191 12715619 1 Renal transplant
127156191 12715619 2 Antiretroviral therapy
127156191 12715619 3 Renal transplant
127156191 12715619 4 Renal transplant

Outcome of event

Event ID CASEID OUTC COD
127156191 12715619 HO

Reactions reported

Event ID CASEID DRUG REC ACT PT
127156191 12715619 Drug interaction
127156191 12715619 Headache
127156191 12715619 Nausea
127156191 12715619 Nephropathy toxic
127156191 12715619 Visual impairment
127156191 12715619 Vomiting

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

no results found

Therapies reported

no results found