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
123497606 12349760 6 F 20160503 20160718 20160510 20160726 EXP US-UNITED THERAPEUTICS-UNT-2016-007286 UNITED THERAPEUTICS 63.00 YR M Y 0.00000 20160726 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
123497606 12349760 1 PS REMODULIN TREPROSTINIL 1 Subcutaneous 0.02 ?G/KG, CONTINUING 21272 .02 UG/KG INJECTION
123497606 12349760 2 SS REMODULIN TREPROSTINIL 1 Subcutaneous 0.01425 ?G/KG, CONTINUING 21272 INJECTION
123497606 12349760 3 SS REMODULIN TREPROSTINIL 1 Subcutaneous 0.01725 ?G/KG, CONTINUING 21272 INJECTION
123497606 12349760 4 SS REMODULIN TREPROSTINIL 1 Subcutaneous 0.0175 ?G/KG, CONTINUING 21272 INJECTION
123497606 12349760 5 SS AMBRISENTAN AMBRISENTAN 1 Unknown 10 MG, QD U U 1504767A 0 10 MG QD
123497606 12349760 6 SS AMBRISENTAN AMBRISENTAN 1 UNK U U 0
123497606 12349760 7 SS ADCIRCA TADALAFIL 1 Unknown U U 0
123497606 12349760 8 C ZOLOFT SERTRALINE HYDROCHLORIDE 1 0
123497606 12349760 9 C DIAZEPAM. DIAZEPAM 1 0
123497606 12349760 10 C SPIRONOLACTONE. SPIRONOLACTONE 1 0
123497606 12349760 11 C TRAMADOL. TRAMADOL 1 0
123497606 12349760 12 C IMODIUM LOPERAMIDE HYDROCHLORIDE 1 0
123497606 12349760 13 C OXYCODONE OXYCODONE 1 0
123497606 12349760 14 C LIPITOR ATORVASTATIN CALCIUM 1 0
123497606 12349760 15 C POTASSIUM POTASSIUM 1 0
123497606 12349760 16 C LEVOXYL LEVOTHYROXINE SODIUM 1 0
123497606 12349760 17 C DIGOXIN. DIGOXIN 1 0
123497606 12349760 18 C WARFARIN WARFARIN 1 0
123497606 12349760 19 C GLIPIZIDE. GLIPIZIDE 1 0
123497606 12349760 20 C METOLAZONE. METOLAZONE 1 0
123497606 12349760 21 C LASIX FUROSEMIDE 1 0
123497606 12349760 22 C TRADJENTA LINAGLIPTIN 1 0
123497606 12349760 23 C BUMEX BUMETANIDE 1 0
123497606 12349760 24 C CARDIZEM CD DILTIAZEM HYDROCHLORIDE 1 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
123497606 12349760 1 Pulmonary arterial hypertension
123497606 12349760 5 Pulmonary arterial hypertension
123497606 12349760 7 Product used for unknown indication
123497606 12349760 8 Product used for unknown indication
123497606 12349760 9 Product used for unknown indication
123497606 12349760 10 Product used for unknown indication
123497606 12349760 11 Product used for unknown indication
123497606 12349760 12 Product used for unknown indication
123497606 12349760 13 Product used for unknown indication
123497606 12349760 14 Product used for unknown indication
123497606 12349760 15 Product used for unknown indication
123497606 12349760 16 Product used for unknown indication
123497606 12349760 17 Product used for unknown indication
123497606 12349760 18 Product used for unknown indication
123497606 12349760 19 Product used for unknown indication
123497606 12349760 20 Product used for unknown indication
123497606 12349760 21 Product used for unknown indication
123497606 12349760 22 Product used for unknown indication
123497606 12349760 23 Product used for unknown indication
123497606 12349760 24 Product used for unknown indication

Outcome of event

Event ID CASEID OUTC COD
123497606 12349760 DE
123497606 12349760 HO

Reactions reported

Event ID CASEID DRUG REC ACT PT
123497606 12349760 Cardiac disorder
123497606 12349760 Fluid retention
123497606 12349760 Malaise
123497606 12349760 Oliguria
123497606 12349760 Pain
123497606 12349760 Renal 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
123497606 12349760 1 20160205 0
123497606 12349760 2 20160424 20160505 0
123497606 12349760 4 20160506 0
123497606 12349760 5 20070717 0
123497606 12349760 6 20121022 20160529 0