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
125376352 12537635 2 F 20000602 20160628 20160707 20160710 EXP GB-TEVA-672075ACC TEVA 49.00 YR M Y 0.00000 20160710 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
125376352 12537635 1 PS PAROXETINE. PAROXETINE 1 40 MILLIGRAM DAILY; 20 MG, BID U U 76618 20 MG TABLET BID
125376352 12537635 2 SS PAROXETINE. PAROXETINE 1 20 MILLIGRAM DAILY; 20 MG, QD U U 76618 20 MG TABLET QD
125376352 12537635 3 SS PAROXETINE HYDROCHLORIDE. PAROXETINE HYDROCHLORIDE 1 Unknown U U 0 TABLET
125376352 12537635 4 SS PAXIL PAROXETINE HYDROCHLORIDE 1 25 MILLIGRAM DAILY; U U 0 25 MG TABLET QD
125376352 12537635 5 SS PAXIL PAROXETINE HYDROCHLORIDE 1 UNK U U 0 TABLET
125376352 12537635 6 SS PAXIL PAROXETINE HYDROCHLORIDE 1 40 MILLIGRAM DAILY; U U 0 20 MG TABLET BID
125376352 12537635 7 SS PAXIL PAROXETINE HYDROCHLORIDE 1 20 MILLIGRAM DAILY; U U 0 20 MG TABLET QD
125376352 12537635 8 SS PAXIL PAROXETINE HYDROCHLORIDE 1 40 MILLIGRAM DAILY; U U 0 20 MG TABLET BID
125376352 12537635 9 C CIPRAMIL CITALOPRAM HYDROBROMIDE 1 UNK 0
125376352 12537635 10 C EFFEXOR VENLAFAXINE HYDROCHLORIDE 1 UNK 0
125376352 12537635 11 C PROTHIADEN DOTHIEPIN HYDROCHLORIDE 1 UNK 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
125376352 12537635 1 Product used for unknown indication
125376352 12537635 3 Panic attack
125376352 12537635 4 Depression
125376352 12537635 5 Product used for unknown indication
125376352 12537635 9 Product used for unknown indication
125376352 12537635 10 Product used for unknown indication
125376352 12537635 11 Product used for unknown indication

Outcome of event

Event ID CASEID OUTC COD
125376352 12537635 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
125376352 12537635 Agitation
125376352 12537635 Blindness transient
125376352 12537635 Disturbance in attention
125376352 12537635 Dizziness
125376352 12537635 Drug withdrawal syndrome
125376352 12537635 Fatigue
125376352 12537635 Irritability
125376352 12537635 Memory impairment
125376352 12537635 Metamorphopsia
125376352 12537635 Mood swings
125376352 12537635 Nightmare
125376352 12537635 Paraesthesia
125376352 12537635 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
125376352 12537635 3 19980603 0
125376352 12537635 4 20150630 0
125376352 12537635 6 20070831 20100729 0
125376352 12537635 7 20100810 20151022 0
125376352 12537635 8 20061213 20070730 0
125376352 12537635 9 19960917 0
125376352 12537635 10 19980601 0