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
125416932 12541693 2 F 19980701 20160720 20160708 20160729 EXP GB-TEVA-673580ACC TEVA 0.00 F Y 0.00000 20160729 CN GB GB

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
125416932 12541693 1 PS PAROXETINE. PAROXETINE 1 Unknown UNK U U 76618 TABLET
125416932 12541693 2 SS PAROXETINE HYDROCHLORIDE. PAROXETINE HYDROCHLORIDE 1 Unknown 10MG/5ML U U 0 ORAL SOLUTION
125416932 12541693 3 SS PAROXETINE HYDROCHLORIDE. PAROXETINE HYDROCHLORIDE 1 Unknown 20 MILLIGRAM DAILY; U U 0 20 MG TABLET QD
125416932 12541693 4 SS SEROXAT PAROXETINE HYDROCHLORIDE 1 Unknown UNK U U 0
125416932 12541693 5 C AMITRIPTYLINE AMITRIPTYLINE 1 UNK 0
125416932 12541693 6 C PROPRANOLOL PROPRANOLOLPROPRANOLOL HYDROCHLORIDE 1 UNK 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
125416932 12541693 1 Depression
125416932 12541693 2 Product used for unknown indication
125416932 12541693 3 Product used for unknown indication
125416932 12541693 4 Product used for unknown indication
125416932 12541693 5 Neuralgia
125416932 12541693 6 Product used for unknown indication

Outcome of event

Event ID CASEID OUTC COD
125416932 12541693 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
125416932 12541693 Abdominal discomfort
125416932 12541693 Aggression
125416932 12541693 Anxiety
125416932 12541693 Apathy
125416932 12541693 Decreased appetite
125416932 12541693 Depressed mood
125416932 12541693 Depression
125416932 12541693 Drug withdrawal syndrome
125416932 12541693 Fatigue
125416932 12541693 Feeling of despair
125416932 12541693 Headache
125416932 12541693 Irritability
125416932 12541693 Mood swings
125416932 12541693 Nausea
125416932 12541693 Palpitations
125416932 12541693 Panic attack
125416932 12541693 Paraesthesia
125416932 12541693 Suicidal ideation
125416932 12541693 Tearfulness
125416932 12541693 Tension
125416932 12541693 Thinking abnormal
125416932 12541693 Tremor

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
125416932 12541693 1 19950530 2004 0
125416932 12541693 2 20010613 20040914 0
125416932 12541693 3 19950530 20030401 0
125416932 12541693 5 20050426 0