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
6382621 7135189 I 6382621-2 20090625 20090916 20090930 EXP DE-MYLANLABS-2009S1016417 MYLAN PHARMACEUTICALS INC. 76 YR M Y 85 KG 20090930 GERMANY

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
6382621 1012354907 PS IBUPROFEN 1 ORAL 70045
6382621 1012354908 I ASPIRIN 1 ORAL
6382621 1012354909 I XIPAMIDE 2 ORAL
6382621 1012354910 C ACTRAPID 2 SUBCUTANEOUS DOSIS/APPLIKATION: 40/36/30
6382621 1012354911 C BISOPROLOL FUMARATE 1 ORAL
6382621 1012354912 C DIGITOXIN INJ 1 ORAL
6382621 1012354913 C METFORMIN HYDROCHLORIDE 1 ORAL
6382621 1012354914 C OMEPRAZOLE 1 ORAL
6382621 1012354915 C PROTAPHANE MC 2 SUBCUTANEOUS

Indications of drugs used

Event ID DRUG SEQ INDI PT
6382621 1012354907 PAIN
6382621 1012354908 CORONARY ARTERY DISEASE
6382621 1012354909 HYPERTENSION
6382621 1012354910 TYPE 2 DIABETES MELLITUS
6382621 1012354911 HYPERTENSION
6382621 1012354912 TACHYARRHYTHMIA
6382621 1012354913 TYPE 2 DIABETES MELLITUS
6382621 1012354914 PROPHYLAXIS AGAINST GASTROINTESTINAL ULCER
6382621 1012354915 TYPE 2 DIABETES MELLITUS

Outcome of event

Event ID OUTC COD
6382621 HO
6382621 LT

Reactions reported

Event ID PT
6382621 DRUG INTERACTION
6382621 RENAL FAILURE ACUTE

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

no results found

Therapies reported

Event ID DRUG SEQ START DT END DT DUR DUR COD
6382621 1012354907 20090311 20090624
6382621 1012354908 20090311
6382621 1012354909 20090311
6382621 1012354910 20090311
6382621 1012354911 20090311 20090624
6382621 1012354912 20090311 20090624
6382621 1012354913 20090311 20090624
6382621 1012354914 20090311
6382621 1012354915 20090311