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
124673874 12467387 4 F 20160816 20160615 20160819 PER US-PFIZER INC-2016297913 PFIZER 0.00 F Y 0.00000 20160819 MD 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
124673874 12467387 1 SS ENBREL ETANERCEPT 1 UNK U 0
124673874 12467387 2 PS ADVIL IBUPROFEN 1 UNK U 18989
124673874 12467387 3 SS CELEBREX CELECOXIB 1 UNK U 20998 CAPSULE, HARD
124673874 12467387 4 SS CODEINE CODEINE 1 UNK U 0
124673874 12467387 5 SS FELDENE PIROXICAM 1 UNK U 18147 CAPSULE, HARD
124673874 12467387 6 SS IBUPROFEN. IBUPROFEN 1 UNK U 18989
124673874 12467387 7 SS METHOTREXATE. METHOTREXATE 1 UNK U 11719
124673874 12467387 8 SS MORPHINE SULFATE. MORPHINE SULFATE 1 UNK U 19999
124673874 12467387 9 SS SULFASALAZINE. SULFASALAZINE 1 UNK U 7073
124673874 12467387 10 SS ACETYLSALICYLIC ACID ASPIRIN 1 UNK U 0
124673874 12467387 11 SS INDOMETHACIN. INDOMETHACIN 1 UNK U 204118
124673874 12467387 12 SS NAPROXEN SODIUM. NAPROXEN SODIUM 1 UNK U 0
124673874 12467387 13 SS ETODOLAC. ETODOLAC 1 UNK U 0
124673874 12467387 14 SS ACTEMRA TOCILIZUMAB 1 UNK U 0
124673874 12467387 15 SS AZATHIOPRINE. AZATHIOPRINE 1 UNK U 0
124673874 12467387 16 SS HUMIRA ADALIMUMAB 1 UNK U 0
124673874 12467387 17 SS LEFLUNOMIDE. LEFLUNOMIDE 1 UNK U 0
124673874 12467387 18 SS MELOXICAM. MELOXICAM 1 UNK U 0
124673874 12467387 19 SS MOBIC MELOXICAM 1 UNK U 0
124673874 12467387 20 SS MOTRIN IBUPROFEN 1 UNK U 0
124673874 12467387 21 SS NABUMETONE. NABUMETONE 1 UNK U 0
124673874 12467387 22 SS ORENCIA ABATACEPT 1 UNK U 0
124673874 12467387 23 SS PLAQUENIL HYDROXYCHLOROQUINE SULFATE 1 UNK U 0
124673874 12467387 24 SS PREDNISONE. PREDNISONE 1 UNK U 0
124673874 12467387 25 SS REMICADE INFLIXIMAB 1 UNK U 0
124673874 12467387 26 SS TYLENOL ACETAMINOPHEN 1 UNK U 0
124673874 12467387 27 SS VIOXX ROFECOXIB 1 UNK U 0

Indications of drugs used

no results found

Outcome of event

no results found

Reactions reported

Event ID CASEID DRUG REC ACT PT
124673874 12467387 Drug hypersensitivity

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

no results found

Therapies reported

no results found