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
125710921 12571092 1 I 20160713 20160719 20160719 EXP BR-SA-2016SA130142 AVENTIS FREIRE PS, MONTONI JD, RIBEIRO ASM, MARQUES HH, MAUAD T, SILVA CA. MILIARY TUBERCULOSIS: A SEVERE OPPORTUNISTIC INFECTION IN JUVENILE SYSTEMIC LUPUS ERYTHEMATOSUS PATIENTS. REV BRAS REUMATOL. 2016;56(3):274-9. AVAILABLE FROM: HTTP://DX.DOI.ORG/10.1016/J.RBRE.2014.04.007. ACCESSED ON: 2014 NOV 28. 20.00 YR A F Y 0.00000 20160719 OT BR BR

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
125710921 12571092 1 SS PREDNISONE. PREDNISONE 1 Intravenous (not otherwise specified) U UNK 0 60 MG QD
125710921 12571092 2 PS CHLOROQUINE PHOSPHATE. CHLOROQUINE PHOSPHATE 1 Unknown U UNK 6002 250 MG QD
125710921 12571092 3 SS METHYLPREDNISOLONE HYDROGEN SUCCINATE METHYLPREDNISOLONE HEMISUCCINATE 1 Unknown U UNK 0 1 G QD
125710921 12571092 4 SS AZATHIOPRINE. AZATHIOPRINE 1 Unknown U UNK 0 100 MG QD

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
125710921 12571092 1 Systemic lupus erythematosus
125710921 12571092 2 Systemic lupus erythematosus
125710921 12571092 3 Systemic lupus erythematosus
125710921 12571092 4 Systemic lupus erythematosus

Outcome of event

Event ID CASEID OUTC COD
125710921 12571092 HO
125710921 12571092 DE

Reactions reported

Event ID CASEID DRUG REC ACT PT
125710921 12571092 Abdominal pain
125710921 12571092 Brain herniation
125710921 12571092 Coma
125710921 12571092 Coma scale abnormal
125710921 12571092 Disseminated tuberculosis
125710921 12571092 Granulomatous liver disease
125710921 12571092 Hepatic necrosis
125710921 12571092 Lung infiltration
125710921 12571092 Papilloedema
125710921 12571092 Peritonitis
125710921 12571092 Pneumonia
125710921 12571092 Pyrexia
125710921 12571092 Sepsis

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

no results found

Therapies reported

no results found