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
126456732 12645673 2 F 201607 20160805 20160811 20160811 EXP US-GLAXOSMITHKLINE-US2016114257 GLAXOSMITHKLINE 81.63 YR F Y 0.00000 20160811 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
126456732 12645673 1 SS ADVAIR DISKUS FLUTICASONE PROPIONATESALMETEROL XINAFOATE 1 Respiratory (inhalation) 1 PUFF(S), BID UNKNOWN 0 1 DF INHALATION POWDER BID
126456732 12645673 2 SS ADVAIR DISKUS FLUTICASONE PROPIONATESALMETEROL XINAFOATE 1 UNK UNKNOWN 0 INHALATION POWDER
126456732 12645673 3 PS VENTOLIN HFA ALBUTEROL SULFATE 1 Respiratory (inhalation) UNK, BID UNKNOWN 20983 BID
126456732 12645673 4 C CARAFATE SUCRALFATE 1 U 0
126456732 12645673 5 C LUMIGAN EYE DROPS 2 U 0
126456732 12645673 6 C HYDROCHLOROTHIAZIDE + TRIAMTERENE HYDROCHLOROTHIAZIDETRIAMTERENE 1 U 0
126456732 12645673 7 C PREDNISONE. PREDNISONE 1 U 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
126456732 12645673 1 Asthma
126456732 12645673 3 Wheezing

Outcome of event

Event ID CASEID OUTC COD
126456732 12645673 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
126456732 12645673 Arthralgia
126456732 12645673 Arthritis
126456732 12645673 Bladder disorder
126456732 12645673 Fall
126456732 12645673 Gait disturbance
126456732 12645673 Glaucoma
126456732 12645673 Urinary incontinence

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

no results found

Therapies reported

no results found