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
126236811 12623681 1 I 20130924 20160804 20160804 PER US-JAZZ-2013-US-001393 JAZZ 0.00 F Y 0.00000 20160804 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
126236811 12623681 1 PS XYREM SODIUM OXYBATE 1 Oral 3 G, BID A22838 21196 3 G ORAL SOLUTION
126236811 12623681 2 SS XYREM SODIUM OXYBATE 1 Oral 4 G, BID A19535 21196 4 G ORAL SOLUTION
126236811 12623681 3 SS XYREM SODIUM OXYBATE 1 Oral 4.5 G, BID A24529 21196 4.5 G ORAL SOLUTION
126236811 12623681 4 SS XYREM SODIUM OXYBATE 1 Oral 4 G, BID 3097762 21196 4 G ORAL SOLUTION
126236811 12623681 5 SS XYREM SODIUM OXYBATE 1 Oral 4.5 G, BID 3101985 21196 4.5 G ORAL SOLUTION
126236811 12623681 6 SS XYREM SODIUM OXYBATE 1 Oral 4 G, BID 21196 4 G ORAL SOLUTION
126236811 12623681 7 SS Antihypertensives UNSPECIFIED INGREDIENT 1 UNK 0
126236811 12623681 8 SS LEVOTHYROXINE SODIUM. LEVOTHYROXINE SODIUM 1 0
126236811 12623681 9 C GEODON ZIPRASIDONE HYDROCHLORIDEIPRASIDONE MESYLATE 1 UNK U 0
126236811 12623681 10 C KLONOPIN CLONAZEPAM 1 UNK U 0
126236811 12623681 11 C ADDERALL AMPHETAMINE ASPARTATEAMPHETAMINE SULFATEDEXTROAMPHETAMINE SACCHARATEDEXTROAMPHETAMINE SULFATE 1 Oral UNK U 0
126236811 12623681 12 C LIDOCAINE. LIDOCAINE 1 UNK U 0
126236811 12623681 13 C ASPIRIN. ASPIRIN 1 Oral UNK, PRN U 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
126236811 12623681 1 Narcolepsy
126236811 12623681 7 Hypertension
126236811 12623681 8 Thyroid disorder
126236811 12623681 9 Product used for unknown indication
126236811 12623681 10 Product used for unknown indication
126236811 12623681 11 Product used for unknown indication
126236811 12623681 12 Pain
126236811 12623681 13 Pain

Outcome of event

no results found

Reactions reported

Event ID CASEID DRUG REC ACT PT
126236811 12623681 Anxiety
126236811 12623681 Body temperature increased
126236811 12623681 Dysstasia
126236811 12623681 Feeling hot
126236811 12623681 Hypothyroidism

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
126236811 12623681 1 200702 2007 0
126236811 12623681 2 200704 2007 0
126236811 12623681 3 200706 2012 0
126236811 12623681 4 201207 2013 0
126236811 12623681 5 201302 2016 0
126236811 12623681 6 201602 0