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
1062533510 10625335 10 F 2000 20160711 20141204 20160725 EXP US-JNJFOC-20141114774 JANSSEN 0.00 C M Y 0.00000 20160725 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
1062533510 10625335 1 SS RISPERDAL RISPERIDONE 1 Oral Y U 0 TABLETS
1062533510 10625335 2 SS RISPERDAL RISPERIDONE 1 Oral Y U 0 TABLETS
1062533510 10625335 3 SS RISPERDAL RISPERIDONE 1 Oral Y U 0 TABLETS
1062533510 10625335 4 PS RISPERDAL RISPERIDONE 1 Oral Y U 20272 TABLETS
1062533510 10625335 5 SS RISPERIDONE. RISPERIDONE 1 Unknown U U 20272 UNSPECIFIED
1062533510 10625335 6 SS SEROQUEL QUETIAPINE FUMARATE 1 Unknown U 0 UNSPECIFIED
1062533510 10625335 7 SS SEROQUEL QUETIAPINE FUMARATE 1 Unknown U 0 UNSPECIFIED
1062533510 10625335 8 SS SEROQUEL QUETIAPINE FUMARATE 1 Unknown U 0 UNSPECIFIED
1062533510 10625335 9 SS DEPAKOTE DIVALPROEX SODIUM 1 Unknown U 0 UNSPECIFIED
1062533510 10625335 10 SS LITHIUM. LITHIUM 1 Oral U 0 UNSPECIFIED

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
1062533510 10625335 1 Abnormal behaviour
1062533510 10625335 2 Depression
1062533510 10625335 3 Attention deficit/hyperactivity disorder
1062533510 10625335 4 Bipolar disorder
1062533510 10625335 5 Product used for unknown indication
1062533510 10625335 6 Depression
1062533510 10625335 7 Bipolar disorder
1062533510 10625335 8 Attention deficit/hyperactivity disorder
1062533510 10625335 9 Product used for unknown indication
1062533510 10625335 10 Product used for unknown indication

Outcome of event

Event ID CASEID OUTC COD
1062533510 10625335 HO
1062533510 10625335 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
1062533510 10625335 Abnormal weight gain
1062533510 10625335 Akathisia
1062533510 10625335 Galactorrhoea
1062533510 10625335 Gynaecomastia
1062533510 10625335 Hallucination, auditory
1062533510 10625335 Hyperprolactinaemia
1062533510 10625335 Mood swings
1062533510 10625335 Rabbit syndrome
1062533510 10625335 Suicidal ideation
1062533510 10625335 Thinking abnormal
1062533510 10625335 Treatment noncompliance
1062533510 10625335 Tremor
1062533510 10625335 Urinary incontinence

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

no results found

Therapies reported

no results found