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
126147811 12614781 1 I 20160720 20160729 20160802 20160802 EXP US-GLAXOSMITHKLINE-US2016110508 GLAXOSMITHKLINE 94.79 YR F Y 0.00000 20160802 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
126147811 12614781 1 PS ANORO ELLIPTA UMECLIDINIUM BROMIDEVILANTEROL TRIFENATATE 1 Respiratory (inhalation) 1 PUFF(S), QD U 6ZP3471 203975 1 DF INHALATION POWDER QD
126147811 12614781 2 SS ANORO ELLIPTA UMECLIDINIUM BROMIDEVILANTEROL TRIFENATATE 1 U 203975 INHALATION POWDER
126147811 12614781 3 SS DUONEB ALBUTEROL SULFATEIPRATROPIUM BROMIDE 1 UNK Y U 0
126147811 12614781 4 C ELIQUIS APIXABAN 1 U 0
126147811 12614781 5 C PREDNISONE. PREDNISONE 1 U 0
126147811 12614781 6 C SPIRONOLACTONE. SPIRONOLACTONE 1 U 0
126147811 12614781 7 C VITAMIN D3 CHOLECALCIFEROL 1 U 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
126147811 12614781 1 Chronic obstructive pulmonary disease
126147811 12614781 2 Asthma
126147811 12614781 3 Product used for unknown indication

Outcome of event

Event ID CASEID OUTC COD
126147811 12614781 DS
126147811 12614781 LT

Reactions reported

Event ID CASEID DRUG REC ACT PT
126147811 12614781 Cough
126147811 12614781 Dyspnoea
126147811 12614781 Nasal congestion
126147811 12614781 Sleep disorder

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
126147811 12614781 1 20160716 0
126147811 12614781 3 20160728 0