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
125096792 12509679 2 F 2016 20160705 20160629 20160714 EXP US-TEVA-670675USA TEVA 0.00 F Y 43.08000 KG 20160714 CN US US

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
125096792 12509679 1 PS FEXOFENADINE FEXOFENADINEFEXOFENADINE HYDROCHLORIDE 1 Oral 180 MILLIGRAM DAILY; N 6BR0168 (43F414) 76191 180 MG ORAL DROPS QD
125096792 12509679 2 SS FEXOFENADINE FEXOFENADINEFEXOFENADINE HYDROCHLORIDE 1 N 6BR0168 (43F414) 76191
125096792 12509679 3 SS FEXOFENADINE FEXOFENADINEFEXOFENADINE HYDROCHLORIDE 1 N 6BR0168 (43F414) 76191
125096792 12509679 4 SS ASPIRIN. ASPIRIN 1 Oral N 0 81 MG
125096792 12509679 5 C FLONASE FLUTICASONE PROPIONATE 1 0
125096792 12509679 6 C CLINDAMYCIN CLINDAMYCINCLINDAMYCIN PHOSPHATE 1 0
125096792 12509679 7 C TYLENOL ARTHRITIS PAIN ACETAMINOPHEN 1 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
125096792 12509679 1 Throat irritation
125096792 12509679 2 Seasonal allergy
125096792 12509679 3 Seasonal allergy
125096792 12509679 4 Cardiovascular event prophylaxis

Outcome of event

Event ID CASEID OUTC COD
125096792 12509679 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
125096792 12509679 Contusion
125096792 12509679 Dizziness
125096792 12509679 Drug administered to patient of inappropriate age
125096792 12509679 Head discomfort
125096792 12509679 Internal haemorrhage
125096792 12509679 Intraocular pressure increased

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

no results found

Therapies reported

Event ID CASEID DSG DRUG SEQ START DT END DT DUR DUR COD
125096792 12509679 1 201604 20160615 0
125096792 12509679 4 2011 20160613 0
125096792 12509679 5 201604 0
125096792 12509679 6 201604 201604 0
125096792 12509679 7 2015 0