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
127421321 12742132 1 I 201408 20140923 20160914 20160914 EXP CA-PFIZER INC-2014264952 PFIZER 55.00 YR F Y 0.00000 20160914 CN 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
127421321 12742132 1 PS XELJANZ TOFACITINIB CITRATE 1 Oral 5 MG, 2X/DAY Y 203214 5 MG TABLET BID
127421321 12742132 2 SS PREDNISONE. PREDNISONE 1 UNK, AS NEEDED Y 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
127421321 12742132 1 Rheumatoid arthritis
127421321 12742132 2 Rheumatoid arthritis

Outcome of event

Event ID CASEID OUTC COD
127421321 12742132 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
127421321 12742132 Bronchitis
127421321 12742132 Erythema
127421321 12742132 Finger deformity
127421321 12742132 Headache
127421321 12742132 Mobility decreased
127421321 12742132 Musculoskeletal disorder
127421321 12742132 Nausea
127421321 12742132 Pain in extremity
127421321 12742132 Peripheral swelling
127421321 12742132 Psychomotor hyperactivity
127421321 12742132 Pyrexia
127421321 12742132 Sensory loss
127421321 12742132 Vomiting
127421321 12742132 Weight 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
127421321 12742132 1 20140812 20151026 0