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 CASE I F COD FOLL SEQ IMAGE EVENT DT MFR DT FDA DT REPT COD MFR NUM MFR SNDR AGE AGE COD GNDR COD E SUB WT WT COD REPT DT OCCP COD DEATH DT TO MFR CONFID REPORTER COUNTRY
6387697 6258537 F 1 6387697-4 20070209 20090914 20090930 EXP MC200700150 THE MEDICINES COMPANY 60 YR M N 108 KG 20090924 MD UNITED STATES

Drug(s) used by person

Event ID DRUG SEQ ROLE COD DRUGNAME VAL VBM ROUTE DOSE VBM DECHAL RECHAL LOT NUM EXP DT NDA NUM
6387697 1012374666 PS ANGIOMAX 1 INTRAVENOUS BOLUS 16 ML, BOLUS, IV BOLUS; 37 ML, HR, INTRAVENOUS Y D 20873
6387697 1012429727 SS CANGRELOR FOR INJECTION (CANGRELOR) INJECTION 2 INTRAVENOUS BOLUS 8 ML, BOLUS, IV BOLUS; 64.2 ML, HR, INTRAVENOUS Y D

Indications of drugs used

Event ID DRUG SEQ INDI PT
6387697 1012374666 PERCUTANEOUS CORONARY INTERVENTION

Outcome of event

Event ID OUTC COD
6387697 HO

Reactions reported

Event ID PT
6387697 CEREBROVASCULAR ACCIDENT
6387697 GINGIVAL BLEEDING
6387697 OPHTHALMOPLEGIA

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

Event ID RPSR COD
6387697 HP

Therapies reported

Event ID DRUG SEQ START DT END DT DUR DUR COD
6387697 1012374666 20070209 20070209
6387697 1012374666 20070209 20070209
6387697 1012429727 20070209 20070209
6387697 1012429727 20070209 20070209