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
122047192 12204719 2 F 201509 20160414 20160323 20160722 EXP NZ-APOTEX-2016AP007182 APOTEX 68.57 YR F Y 0.00000 20160722 CN NZ NZ

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
122047192 12204719 1 PS DILTIAZEM. DILTIAZEM 1 Oral 180 MG, A DAY 74943 180 MG
122047192 12204719 2 SS DILTIAZEM. DILTIAZEM 1 Oral 120 MG, A DAY 74943 120 MG
122047192 12204719 3 C LIPEX /00848101/ 2 Unknown 40 MG, X1 DAY U 0 40 MG
122047192 12204719 4 C LOSEC OMEPRAZOLE 1 Unknown 20 MG, X1 U 0 20 MG
122047192 12204719 5 C NOVORAPID INSULIN ASPART 1 Unknown 7 UNITS 3X PER DAY U 0 7 DF TID
122047192 12204719 6 C LANTUS INSULIN GLARGINE 1 38 1DF X1 DAY U 0 1 DF

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
122047192 12204719 1 Hypertension
122047192 12204719 3 Product used for unknown indication
122047192 12204719 4 Product used for unknown indication
122047192 12204719 5 Diabetes mellitus
122047192 12204719 6 Diabetes mellitus

Outcome of event

Event ID CASEID OUTC COD
122047192 12204719 DS

Reactions reported

Event ID CASEID DRUG REC ACT PT
122047192 12204719 Constipation
122047192 12204719 Dry mouth
122047192 12204719 Palpitations
122047192 12204719 Photophobia

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
122047192 12204719 1 20160307 20160313 0
122047192 12204719 2 201509 20160313 0