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
123133162 12313316 2 F 20160924 20160428 20160926 PER US-PFIZER INC-2016200612 PFIZER 71.00 YR F Y 0.00000 20160926 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
123133162 12313316 1 PS ALAVERT ALLERGY LORATADINE 1 Oral 10MG, DISINTEGRATING TABLET, ONCE A DAY K00414 21375 10 MG ORODISPERSIBLE TABLET QD
123133162 12313316 2 SS ALAVERT ALLERGY LORATADINE 1 21375 ORODISPERSIBLE TABLET
123133162 12313316 3 SS ALAVERT ALLERGY LORATADINE 1 21375 ORODISPERSIBLE TABLET
123133162 12313316 4 SS ALAVERT ALLERGY LORATADINE 1 21375 ORODISPERSIBLE TABLET
123133162 12313316 5 SS IBUPROFEN. IBUPROFEN 1 Oral 1 DF, DAILY 18989 1 DF TABLET
123133162 12313316 6 SS BENADRYL DIPHENHYDRAMINE HYDROCHLORIDE 1 UNK U 0
123133162 12313316 7 SS LETROZOLE. LETROZOLE 1 Oral 2.5 MG, DAILY 0 2.5 MG TABLET

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
123133162 12313316 1 Lacrimation increased
123133162 12313316 2 Rhinorrhoea
123133162 12313316 3 Eye pruritus
123133162 12313316 4 Drug reaction with eosinophilia and systemic symptoms
123133162 12313316 7 Breast cancer

Outcome of event

no results found

Reactions reported

Event ID CASEID DRUG REC ACT PT
123133162 12313316 Condition aggravated
123133162 12313316 Drug ineffective
123133162 12313316 Myalgia

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
123133162 12313316 1 2015 0
123133162 12313316 7 2011 0