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
93423104 9342310 4 F 20130530 20160719 20130611 20160722 EXP PHHY2013CA056631 NOVARTIS 37.64 YR F Y 0.00000 20160722 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
93423104 9342310 1 PS GILENYA FINGOLIMOD HYDROCHLORIDE 1 Oral 0.5 MG, QD Y S0034 22527 .5 MG CAPSULE QD
93423104 9342310 2 C VITAMIN D CHOLECALCIFEROL 1 Unknown 1000 MG, QD U 0 1000 MG TABLET QD
93423104 9342310 3 C PANTOPRAZOLE PANTOPRAZOLE SODIUM 1 Unknown 40 MG, QD U 0 40 MG TABLET QD
93423104 9342310 4 C TOVIAZ FESOTERODINE FUMARATE 1 Unknown 8 MG, QD U 0 8 MG TABLET QD
93423104 9342310 5 C PREGABALIN. PREGABALIN 1 Oral 300 MG, QD U 0 300 MG TABLET QD
93423104 9342310 6 C BACLOFEN. BACLOFEN 1 Unknown 10 MG, QD U 0 10 MG TABLET QD

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
93423104 9342310 1 Relapsing-remitting multiple sclerosis
93423104 9342310 2 Product used for unknown indication
93423104 9342310 3 Product used for unknown indication
93423104 9342310 4 Product used for unknown indication
93423104 9342310 5 Product used for unknown indication
93423104 9342310 6 Product used for unknown indication

Outcome of event

Event ID CASEID OUTC COD
93423104 9342310 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
93423104 9342310 Blood pressure decreased
93423104 9342310 Burning sensation
93423104 9342310 Dizziness
93423104 9342310 Headache
93423104 9342310 Hypoaesthesia
93423104 9342310 Pain in extremity

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
93423104 9342310 1 20130530 0