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
5742761 6643489 I 5742761-5 20071127 20080509 20080519 EXP CG-MERCK-0805USA02242 MERCK HUMAN HEALTH DIVISION 32 YR M Y 20080520 MD CONGO

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
5742761 1009925562 PS STROMECTOL 1 ORAL 050742

Indications of drugs used

Event ID DRUG SEQ INDI PT
5742761 1009925562 ONCHOCERCIASIS

Outcome of event

Event ID OUTC COD
5742761 HO

Reactions reported

Event ID PT
5742761 ASTHENIA
5742761 BACK PAIN
5742761 CONJUNCTIVAL HAEMORRHAGE
5742761 HEADACHE
5742761 LOGORRHOEA
5742761 PRURITUS

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
5742761 1009925562 20071126 20071126 1 DAY