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
127207251 12720725 1 I 20151008 20160826 20160907 20160907 EXP FR-AFSSAPS-NC20151028 FR-FRI-1000087377 FOREST 84.30 YR F Y 0.00000 20160907 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
127207251 12720725 1 PS ESCITALOPRAM ESCITALOPRAM OXALATE 1 Oral DAILY DOSE NOT REPORTED Y 21323
127207251 12720725 2 SS CARDENSIEL BISOPROLOL FUMARATE 1 Oral DAILY DOSE NOT REPORTED 0
127207251 12720725 3 SS KARDEGIC ASPIRIN LYSINE 1 Oral DAILY DOSE NOT REPORTED 0
127207251 12720725 4 SS LEVOTHYROX LEVOTHYROXINE 1 Oral DAILY DOSE NOT REPORTED 0
127207251 12720725 5 SS CRESTOR ROSUVASTATIN CALCIUM 1 Oral DAILY DOSE NOT REPORTED 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
127207251 12720725 1 Product used for unknown indication
127207251 12720725 2 Product used for unknown indication
127207251 12720725 3 Product used for unknown indication
127207251 12720725 4 Product used for unknown indication
127207251 12720725 5 Product used for unknown indication

Outcome of event

Event ID CASEID OUTC COD
127207251 12720725 HO

Reactions reported

Event ID CASEID DRUG REC ACT PT
127207251 12720725 Fall
127207251 12720725 General physical health deterioration
127207251 12720725 Hypokalaemia
127207251 12720725 Hyponatraemia

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

no results found

Therapies reported

no results found