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
5285252 6523890 I 5285252-0 20070208 20070322 20070403 EXP GB-PFIZER INC-2007023501 PFIZER INC 43 YR M Y 20070403 OT UNITED KINGDOM

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
5285252 1008326781 PS AZITHROMYCIN 1 ORAL 50670
5285252 1008326782 SS CEFIXIME CHEWABLE 1 ORAL

Indications of drugs used

no results found

Outcome of event

Event ID OUTC COD
5285252 OT

Reactions reported

Event ID PT
5285252 COUGH
5285252 DIARRHOEA
5285252 GASTROINTESTINAL DISORDER
5285252 PHARYNGOLARYNGEAL PAIN
5285252 PRODUCTIVE COUGH
5285252 SWELLING FACE
5285252 VOMITING

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
5285252 1008326781 20070208 20070208
5285252 1008326782 20070207 20070207