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
109732314 10973231 4 F 20141215 20160802 20150401 20160809 EXP DE-ABBVIE-15K-062-1366915-00 ABBVIE 77.99 YR F Y 0.00000 20160809 CN COUNTRY NOT SPECIFIED DE

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
109732314 10973231 1 PS HUMIRA ADALIMUMAB 1 Subcutaneous Y UNKNOWN 125057 40 MG SOLUTION FOR INJECTION IN PRE-FILLED SYRINGE
109732314 10973231 2 SS HUMIRA ADALIMUMAB 1 Subcutaneous Y UNKNOWN 125057 SOLUTION FOR INJECTION IN PRE-FILLED SYRINGE
109732314 10973231 3 SS HUMIRA ADALIMUMAB 1 Subcutaneous Y UNKNOWN 125057 SOLUTION FOR INJECTION IN PRE-FILLED SYRINGE
109732314 10973231 4 C INSULIN INSULIN NOS 1 0
109732314 10973231 5 C TILIDIN NALOXONE HYDROCHLORIDETILIDINE HYDROCHLORIDE 1 50/4 0 TID
109732314 10973231 6 C NOVALGIN METAMIZOLE SODIUM 1 0 600 MG QID

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
109732314 10973231 1 Rheumatoid arthritis
109732314 10973231 4 Product used for unknown indication
109732314 10973231 5 Product used for unknown indication
109732314 10973231 6 Product used for unknown indication

Outcome of event

Event ID CASEID OUTC COD
109732314 10973231 OT
109732314 10973231 HO

Reactions reported

Event ID CASEID DRUG REC ACT PT
109732314 10973231 Ascites
109732314 10973231 Cholelithiasis
109732314 10973231 Herpes zoster
109732314 10973231 Malaise
109732314 10973231 Oedema peripheral
109732314 10973231 Renal failure
109732314 10973231 Renal function test abnormal

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
109732314 10973231 1 20110401 20150106 0
109732314 10973231 2 2015 201508 0
109732314 10973231 3 2015 201511 0
109732314 10973231 5 201511 0