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
6389401 7140315 I 6389401-2 20090924 20091006 EXP US-JNJFOC-20090907793 MCNEIL CONSUMER HEALTHCARE 7 YR F Y 22.68 KG 20091006 CN 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
6389401 1012381353 PS CHILDREN'S TYLENOL SUSPENSION 1 ORAL SBM042 19872
6389401 1012381354 SS CHILDREN'S TYLENOL SUSPENSION 1 ORAL SBM042 019872

Indications of drugs used

Event ID DRUG SEQ INDI PT
6389401 1012381354 ABDOMINAL PAIN UPPER

Outcome of event

Event ID OUTC COD
6389401 OT

Reactions reported

Event ID PT
6389401 CYCLIC VOMITING SYNDROME
6389401 TRANSMISSION OF AN INFECTIOUS AGENT VIA A MEDICINAL PRODUCT

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

no results found

Therapies reported

no results found