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
126903941 12690394 1 I 2014 20160329 20160826 20160826 PER US-FRI-1000083703 FOREST 10.00 YR F Y 0.00000 20160826 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
126903941 12690394 1 PS LEXAPRO ESCITALOPRAM OXALATE 1 Oral 2.5MG 21323 2.5 MG TABLETS QD
126903941 12690394 2 SS LEXAPRO ESCITALOPRAM OXALATE 1 Oral 5MG 21323 5 MG TABLETS QD
126903941 12690394 3 SS LEXAPRO ESCITALOPRAM OXALATE 1 Oral 7.5MG 0 7.5 MG TABLETS QD
126903941 12690394 4 SS LEXAPRO ESCITALOPRAM OXALATE 1 Oral 10MG 0 10 MG TABLETS
126903941 12690394 5 SS LEXAPRO ESCITALOPRAM OXALATE 1 Oral 7.5MG 0 7.5 MG TABLETS QD
126903941 12690394 6 C TYLENOL ACETAMINOPHEN 1 0
126903941 12690394 7 C TYLENOL ACETAMINOPHEN 1 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
126903941 12690394 1 Depression
126903941 12690394 6 Headache
126903941 12690394 7 Pain

Outcome of event

no results found

Reactions reported

Event ID CASEID DRUG REC ACT PT
126903941 12690394 Abdominal pain upper
126903941 12690394 Arthralgia
126903941 12690394 Fatigue
126903941 12690394 Headache
126903941 12690394 Intentional product misuse
126903941 12690394 Nausea
126903941 12690394 Pain in extremity
126903941 12690394 Paraesthesia
126903941 12690394 Photosensitivity reaction
126903941 12690394 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
126903941 12690394 1 20140425 0
126903941 12690394 4 20160325 0
126903941 12690394 5 20160326 0