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
126341861 12634186 1 I 20160722 0 20160808 20160808 DIR 76.00 YR M N 0.00000 20160805 Y PH US

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
126341861 12634186 1 PS AMPYRA DALFAMPRIDINE 1 Oral D D TCNV 20180430 0 10 MG BID
126341861 12634186 2 C EXTAVIA INTERFERON BETA-1B 1 0
126341861 12634186 3 C FOSAMAX ALENDRONATE SODIUM 1 0
126341861 12634186 4 C KEFLEX CEPHALEXIN 1 0
126341861 12634186 5 C CHOLECALCIFEROL CHOLECALCIFEROL 1 0
126341861 12634186 6 C VITAMIN D3 CHOLECALCIFEROL 1 0
126341861 12634186 7 C ATENOLOL. ATENOLOL 1 0
126341861 12634186 8 C SIMVASTATIN. SIMVASTATIN 1 0
126341861 12634186 9 C LISINOPRIL AND HYDROCHLOROTHIAZIDE HYDROCHLOROTHIAZIDELISINOPRIL 1 0
126341861 12634186 10 C POLYTRIM POLYMYXIN B SULFATETRIMETHOPRIM SULFATE 1 0
126341861 12634186 11 C ACULAR KETOROLAC TROMETHAMINE 1 0
126341861 12634186 12 C PRED FORTE PREDNISOLONE ACETATE 1 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
126341861 12634186 1 Multiple sclerosis

Outcome of event

no results found

Reactions reported

Event ID CASEID DRUG REC ACT PT
126341861 12634186 Laboratory test abnormal

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

Event ID CASEID RPSR COD
126341861 12634186 HP
126341861 12634186 UF

Therapies reported

Event ID CASEID DSG DRUG SEQ START DT END DT DUR DUR COD
126341861 12634186 1 201607 0