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
125940041 12594004 1 I 201511 20151119 20160726 20160726 PER US-UNITED THERAPEUTICS-UNT-2015-014829 UNITED THERAPEUTICS 60.32 YR F Y 54.42000 KG 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
125940041 12594004 1 PS TYVASO TREPROSTINIL 1 72 ?G, QID 2100675 22387 72 UG INHALATION GAS QID
125940041 12594004 2 SS TYVASO TREPROSTINIL 1 UNK 2100699 22387 INHALATION GAS
125940041 12594004 3 SS TYVASO TREPROSTINIL 1 UNK 2100711 22387 INHALATION GAS
125940041 12594004 4 SS LETAIRIS AMBRISENTAN 1 Unknown 10 MG, UNK SBFT 0 10 MG TABLET
125940041 12594004 5 SS LETAIRIS AMBRISENTAN 1 Unknown UNK 1500226A 0 TABLET
125940041 12594004 6 SS REVATIO SILDENAFIL CITRATE 1 Unknown U U 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
125940041 12594004 1 Pulmonary arterial hypertension
125940041 12594004 4 Product used for unknown indication
125940041 12594004 6 Product used for unknown indication

Outcome of event

no results found

Reactions reported

Event ID CASEID DRUG REC ACT PT
125940041 12594004 Cough
125940041 12594004 Dizziness
125940041 12594004 Malaise
125940041 12594004 Nasopharyngitis
125940041 12594004 Presyncope
125940041 12594004 Product use issue

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
125940041 12594004 1 20141222 0
125940041 12594004 4 20120321 0