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
104368112 10436811 2 F 20160715 20140908 20160715 PER US-BRISTOL-MYERS SQUIBB COMPANY-20243036 BRISTOL MYERS SQUIBB 0.00 M Y 0.00000 20160715 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
104368112 10436811 1 PS ABILIFY ARIPIPRAZOLE 1 Unknown DOSE INCREASED TO 10 MG/DAY U 2E716 21436 5 MG TABLET QD
104368112 10436811 2 SS ABILIFY ARIPIPRAZOLE 1 U 21436 TABLET
104368112 10436811 3 SS ABILIFY ARIPIPRAZOLE 1 U 21436 TABLET
104368112 10436811 4 SS ABILIFY ARIPIPRAZOLE 1 U 21436 TABLET
104368112 10436811 5 SS LATUDA LURASIDONE HYDROCHLORIDE 1 Oral 1 TABLET IN BY MOUTH IN MORNING U 0 80 MG
104368112 10436811 6 C HYDROXYZINE HYDROXYZINEHYDROXYZINE HYDROCHLORIDE 1 Oral AS NEEDED U 0 25 MG TID
104368112 10436811 7 C DEPAKOTE ER DIVALPROEX SODIUM 1 Unknown 1 TABLET IN MORNING AND 2 TABLETS AT BEDTIME U 0 500 MG
104368112 10436811 8 C DEPAKOTE DIVALPROEX SODIUM 1 Oral 1 TABLET BY MOUTH IN MORNING U 0 250 MG
104368112 10436811 9 C SEROQUEL QUETIAPINE FUMARATE 1 Oral 2 TABLETS BY MOUTH EVERY EVENING,50 MG 1 TABLET BY MOUTH DAILY AS NEEDED U 0 400 MG
104368112 10436811 10 C BENZTROPINE MESYLATE. BENZTROPINE MESYLATE 1 Unknown AS NEEDED U 0 1 MG BID

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
104368112 10436811 1 Schizophrenia
104368112 10436811 2 Bipolar disorder
104368112 10436811 3 Avoidant personality disorder
104368112 10436811 4 Obsessive-compulsive disorder
104368112 10436811 5 Product used for unknown indication
104368112 10436811 6 Product used for unknown indication
104368112 10436811 7 Product used for unknown indication
104368112 10436811 8 Product used for unknown indication
104368112 10436811 9 Product used for unknown indication
104368112 10436811 10 Product used for unknown indication

Outcome of event

no results found

Reactions reported

Event ID CASEID DRUG REC ACT PT
104368112 10436811 Aggression
104368112 10436811 Hallucinations, mixed
104368112 10436811 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
104368112 10436811 1 201309 0