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
106221696 10622169 6 F 20140726 20160901 20141203 20160907 EXP PHFR2014GB005580 NOVARTIS 49.86 YR F Y 0.00000 20160907 MD GB GB

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
106221696 10622169 1 PS GILENYA FINGOLIMOD HYDROCHLORIDE 1 Oral 0.5 MG, QD 2.5 MG Y U 22527 .5 MG CAPSULE QD
106221696 10622169 2 SS COPAXONE GLATIRAMER ACETATE 1 Unknown U 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
106221696 10622169 1 Multiple sclerosis
106221696 10622169 2 Product used for unknown indication

Outcome of event

Event ID CASEID OUTC COD
106221696 10622169 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
106221696 10622169 Coordination abnormal
106221696 10622169 Depressed mood
106221696 10622169 Facial paralysis
106221696 10622169 Flushing
106221696 10622169 Malaise
106221696 10622169 Mobility decreased
106221696 10622169 Multiple sclerosis relapse
106221696 10622169 Nausea
106221696 10622169 Pain
106221696 10622169 Paralysis
106221696 10622169 Paresis
106221696 10622169 Skin reaction
106221696 10622169 Suicidal ideation
106221696 10622169 Vision blurred
106221696 10622169 Vomiting

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
106221696 10622169 1 20140722 20140731 0