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
125372301 12537230 1 I 2012 20151230 20160707 20160707 PER US-JAZZ-2015-US-022744 JAZZ 0.00 M Y 0.00000 20160707 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
125372301 12537230 1 PS XYREM SODIUM OXYBATE 1 Oral 2.25 G, BID 21196 2.25 G ORAL SOLUTION
125372301 12537230 2 SS XYREM SODIUM OXYBATE 1 Oral DOSE ADJUSTMENTS 21196 ORAL SOLUTION
125372301 12537230 3 SS XYREM SODIUM OXYBATE 1 Oral 4 G, BID 21196 4 G ORAL SOLUTION
125372301 12537230 4 SS XYREM SODIUM OXYBATE 1 Oral 3 G, BID 21196 3 G ORAL SOLUTION
125372301 12537230 5 SS XYREM SODIUM OXYBATE 1 Oral DOSE ADJUSTMENTS 21196 ORAL SOLUTION
125372301 12537230 6 SS XYREM SODIUM OXYBATE 1 Oral 4 G, BID 21196 4 G ORAL SOLUTION
125372301 12537230 7 SS XYREM SODIUM OXYBATE 1 Oral 4.5 G, BID 21196 4.5 G ORAL SOLUTION
125372301 12537230 8 SS STRATTERA ATOMOXETINE HYDROCHLORIDE 1 UNK N 0
125372301 12537230 9 SS CONCERTA METHYLPHENIDATE HYDROCHLORIDE 1 UNK N 0
125372301 12537230 10 C CHOLESTYRAMINE. CHOLESTYRAMINE 1 UNK U 0
125372301 12537230 11 C DICYCLOMINE DICYCLOMINE HYDROCHLORIDE 1 UNK U 0
125372301 12537230 12 C PROVIGIL MODAFINIL 1 UNK U 0
125372301 12537230 13 C Vitamins VITAMINS 1 UNK U 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
125372301 12537230 1 Narcolepsy
125372301 12537230 8 Product used for unknown indication
125372301 12537230 9 Product used for unknown indication
125372301 12537230 10 Product used for unknown indication
125372301 12537230 11 Product used for unknown indication
125372301 12537230 12 Product used for unknown indication
125372301 12537230 13 Product used for unknown indication

Outcome of event

Event ID CASEID OUTC COD
125372301 12537230 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
125372301 12537230 Epigastric discomfort
125372301 12537230 Irritable bowel syndrome
125372301 12537230 Weight decreased

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
125372301 12537230 1 200809 200809 0
125372301 12537230 2 2008 2009 0
125372301 12537230 3 200910 2010 0
125372301 12537230 4 201103 2011 0
125372301 12537230 5 2011 2011 0
125372301 12537230 6 2011 2012 0
125372301 12537230 7 201206 0
125372301 12537230 8 20101210 20131210 0
125372301 12537230 9 20121210 0
125372301 12537230 10 20101210 20131210 0
125372301 12537230 11 20101210 20131210 0
125372301 12537230 12 20101210 20131210 0
125372301 12537230 13 20101210 20111210 0