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
125830701 12583070 1 I 20160714 20160722 20160722 EXP CA-PFIZER INC-2016356000 PFIZER 45.00 YR F Y 0.00000 20160722 OT CA CA

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
125830701 12583070 1 SS ENBREL ETANERCEPT 1 Oral 25 MG, 1X/DAY U 0 25 MG QD
125830701 12583070 2 SS ENBREL ETANERCEPT 1 Subcutaneous 50 MG, 1X/DAY U 0 50 MG QD
125830701 12583070 3 PS RAPAMUNE SIROLIMUS 1 UNK U 21110
125830701 12583070 4 SS DACLIZUMAB DACLIZUMAB 1 UNK U 0
125830701 12583070 5 SS MYCOPHENOLATE MOFETIL. MYCOPHENOLATE MOFETIL 1 Oral 1000 MG, 2X/DAY U 0 1000 MG BID
125830701 12583070 6 SS NEORAL CYCLOSPORINE 1 UNK U 0
125830701 12583070 7 SS PROGRAF TACROLIMUSTACROLIMUS ANHYDROUS 1 Oral 3 MG, 2X/DAY U 0 3 MG BID
125830701 12583070 8 SS PROGRAF TACROLIMUSTACROLIMUS ANHYDROUS 1 Oral 2 MG, 2X/DAY U 0 2 MG BID
125830701 12583070 9 SS PROGRAF TACROLIMUSTACROLIMUS ANHYDROUS 1 UNK U 0
125830701 12583070 10 SS REMICADE INFLIXIMAB 1 Intravenous (not otherwise specified) UNK U 0

Indications of drugs used

no results found

Outcome of event

Event ID CASEID OUTC COD
125830701 12583070 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
125830701 12583070 Acne
125830701 12583070 Alopecia
125830701 12583070 Ovarian cyst
125830701 12583070 Product use issue
125830701 12583070 Transplant dysfunction
125830701 12583070 Transplant rejection

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

no results found

Therapies reported

no results found