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 CASE I F COD FOLL SEQ IMAGE EVENT DT MFR DT FDA DT REPT COD MFR NUM MFR SNDR AGE AGE COD GNDR COD E SUB WT WT COD REPT DT OCCP COD DEATH DT TO MFR CONFID REPORTER COUNTRY
5904419 6781921 I 5904419-9 20080930 DIR 6 YR F N 49 LBS 20080929 CN N N UNITED STATES

Drug(s) used by person

Event ID DRUG SEQ ROLE COD DRUGNAME VAL VBM ROUTE DOSE VBM DECHAL RECHAL LOT NUM EXP DT NDA NUM
5904419 1010523904 PS SINGULAIR 1 ORAL 5 MG CHEW TABLET ONCE/DAY PO Y D

Indications of drugs used

Event ID DRUG SEQ INDI PT
5904419 1010523904 MULTIPLE ALLERGIES

Outcome of event

Event ID OUTC COD
5904419 OT

Reactions reported

Event ID PT
5904419 ABNORMAL BEHAVIOUR
5904419 AGGRESSION
5904419 ANGER
5904419 ANXIETY
5904419 EMOTIONAL DISORDER
5904419 HALLUCINATION
5904419 HEADACHE
5904419 NERVOUSNESS
5904419 PAIN IN EXTREMITY

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

no results found

Therapies reported

Event ID DRUG SEQ START DT END DT DUR DUR COD
5904419 1010523904 20080522 20080902