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
127110011 12711001 1 I 20160824 20160902 20160902 EXP DK-DKMA-ADR 23619344 DK-FRI-1000087230 FOREST 0.00 M Y 0.00000 20160902 OT DK DK

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
127110011 12711001 1 PS ESCITALOPRAM ESCITALOPRAM OXALATE 1 Unknown U 21323 TABLET
127110011 12711001 2 SS ESCITALOPRAM ESCITALOPRAM OXALATE 1 Oral U 21323 FILM-COATED TABLET
127110011 12711001 3 SS IMOCLONE ZOPICLONE 1 Unknown U U 0
127110011 12711001 4 SS IMOCLONE ZOPICLONE 1 Oral U U 0 FILM-COATED TABLET
127110011 12711001 5 SS OXAPAX OXAZEPAM 1 Oral U U 0 TABLET
127110011 12711001 6 SS SEROQUEL QUETIAPINE FUMARATE 1 Oral U U 0 FILM-COATED TABLET
127110011 12711001 7 SS SEROQUEL XR QUETIAPINE FUMARATE 1 Oral U 0 PROLONGED-RELEASE TABLET
127110011 12711001 8 SS ABILIFY ARIPIPRAZOLE 1 Oral U 0
127110011 12711001 9 SS TRUXAL CHLORPROTHIXENE 1 Oral U U 0 265 MG FILM-COATED TABLET
127110011 12711001 10 SS ZELDOX ZIPRASIDONE 1 Oral DOSE: 80 MG INCREASING TO 160 MG U U 0
127110011 12711001 11 SS SOLIAN AMISULPRIDE 1 Oral U U 0 TABLET
127110011 12711001 12 SS RISPERIDON ^KRKA^ RISPERIDONE 1 Oral U U 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
127110011 12711001 1 Depression
127110011 12711001 3 Insomnia
127110011 12711001 5 Sedation
127110011 12711001 6 Schizophrenia
127110011 12711001 7 Schizophrenia
127110011 12711001 8 Schizophrenia
127110011 12711001 9 Schizophrenia
127110011 12711001 10 Schizophrenia
127110011 12711001 11 Schizophrenia
127110011 12711001 12 Schizophrenia

Outcome of event

Event ID CASEID OUTC COD
127110011 12711001 HO

Reactions reported

Event ID CASEID DRUG REC ACT PT
127110011 12711001 Depressed mood
127110011 12711001 Intentional overdose
127110011 12711001 Restlessness
127110011 12711001 Sedation
127110011 12711001 Social avoidant behaviour
127110011 12711001 Suicidal ideation
127110011 12711001 Suicide attempt
127110011 12711001 Weight increased

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
127110011 12711001 1 20110926 20120120 0
127110011 12711001 2 20120611 201208 0
127110011 12711001 3 20110926 20120120 0
127110011 12711001 4 20120611 0
127110011 12711001 5 20120629 0
127110011 12711001 6 20120625 20120822 0
127110011 12711001 7 20120822 201208 0
127110011 12711001 8 20120822 201208 0
127110011 12711001 9 20120831 0
127110011 12711001 10 20120925 0
127110011 12711001 11 20121121 0
127110011 12711001 12 20150115 0