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
110206174 11020617 4 F 20150306 20160804 20150413 20160811 EXP CA-AMGEN-CANSP2015023435 AMGEN 63.00 YR A F Y 0.00000 20160811 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
110206174 11020617 1 PS ENBREL ETANERCEPT 1 Subcutaneous 50 MG, WEEKLY 103795 50 MG UNKNOWN FORMULATION /wk
110206174 11020617 2 SS PLAQUENIL HYDROXYCHLOROQUINE SULFATE 1 Unknown UNK 0 TABLET
110206174 11020617 3 SS ORENCIA ABATACEPT 1 Unknown UNK 0
110206174 11020617 4 C XELJANZ TOFACITINIB CITRATE 1 Oral 5 MG, 2X/DAY 0 5 MG BID
110206174 11020617 5 C LYRICA PREGABALIN 1 Oral UNK 0
110206174 11020617 6 C HYDROMORPHONE HYDROMORPHONE 1 UNK 0
110206174 11020617 7 C HYDROMORPH CONTIN HYDROMORPHONE 1 UNK 0
110206174 11020617 8 C CYMBALTA DULOXETINE HYDROCHLORIDE 1 UNK 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
110206174 11020617 1 Rheumatoid arthritis
110206174 11020617 2 Product used for unknown indication
110206174 11020617 3 Product used for unknown indication
110206174 11020617 4 Rheumatoid arthritis

Outcome of event

Event ID CASEID OUTC COD
110206174 11020617 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
110206174 11020617 Arthropathy
110206174 11020617 Drug ineffective
110206174 11020617 Pain
110206174 11020617 Rheumatoid arthritis
110206174 11020617 Shoulder operation
110206174 11020617 Therapeutic response decreased

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
110206174 11020617 1 2010 0
110206174 11020617 4 20150401 0