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
126271862 12627186 2 F 20160630 20160909 20160805 20160921 EXP FR-AFSSAPS-PA20160637 FR-FRI-1000086671 FOREST 22.87 YR F Y 0.00000 20160921 OT DK FR

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
126271862 12627186 1 PS ESCITALOPRAM ESCITALOPRAM OXALATE 1 Oral 10 MG Y 21323 10 MG QD
126271862 12627186 2 SS ESCITALOPRAM ESCITALOPRAM OXALATE 1 Oral OVERDOSE: ESCITALOPRAM 280 MG AT ONCE. Y 21323 280 MG
126271862 12627186 3 SS DOXYLAMINE DOXYLAMINE 1 Oral Y 0
126271862 12627186 4 SS NOCERTONE OXETORONE 1 Oral Y 0 1.2 G
126271862 12627186 5 SS CODEINE CODEINE 1 Oral Y 0 120 MG
126271862 12627186 6 C PARACETAMOL ACETAMINOPHEN 1 Oral 0 2 G
126271862 12627186 7 C KETOPROFENE KETOPROFEN 1 Oral 0 700 MG
126271862 12627186 8 C KETOPROFENE KETOPROFEN 1 Oral OVERDOSE: KETOPROFENE 700 MG AT ONCE. 0 700 MG
126271862 12627186 9 C JASMINELLE DROSPIRENONE 1 Unknown 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
126271862 12627186 1 Depression
126271862 12627186 3 Product used for unknown indication
126271862 12627186 4 Product used for unknown indication
126271862 12627186 5 Product used for unknown indication
126271862 12627186 6 Product used for unknown indication
126271862 12627186 7 Product used for unknown indication

Outcome of event

Event ID CASEID OUTC COD
126271862 12627186 HO

Reactions reported

Event ID CASEID DRUG REC ACT PT
126271862 12627186 Dry mouth
126271862 12627186 Miosis
126271862 12627186 Somnolence

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
126271862 12627186 1 20160630 0
126271862 12627186 2 20160630 20160630 0
126271862 12627186 3 20160630 0
126271862 12627186 4 20160630 20160630 0
126271862 12627186 5 20160630 20160630 0
126271862 12627186 6 20160630 20160630 0
126271862 12627186 7 20160630 0
126271862 12627186 8 20160630 20160630 0