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
127819441 12781944 1 I 20160606 20160915 20160926 20160926 EXP GB-MHRA-EYC 00145163 GB-CONCORDIA PHARMACEUTICALS INC.-GSH201609-004652 CONCORDIA 0.00 F Y 0.00000 20160927 OT 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
127819441 12781944 1 PS DIGOXIN. DIGOXIN 1 Oral IN THE MORNING D U 20405 QD
127819441 12781944 2 SS LISINOPRIL. LISINOPRIL 1 Oral D U 0 20 MG QD
127819441 12781944 3 C AMLODIPINE AMLODIPINE BESYLATE 1 0
127819441 12781944 4 C FOSTAIR BECLOMETHASONEFORMOTEROL 1 0
127819441 12781944 5 C FUROSEMIDE. FUROSEMIDE 1 0
127819441 12781944 6 C IBANDRONIC ACID IBANDRONIC ACID 1 0
127819441 12781944 7 C LEFLUNOMIDE. LEFLUNOMIDE 1 0
127819441 12781944 8 C OMEPRAZOLE. OMEPRAZOLE 1 0
127819441 12781944 9 C TIOTROPIUM BROMIDE TIOTROPIUM BROMIDE 1 0
127819441 12781944 10 C WARFARIN WARFARIN 1 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
127819441 12781944 1 Atrial fibrillation
127819441 12781944 2 Hypertension

Outcome of event

Event ID CASEID OUTC COD
127819441 12781944 HO

Reactions reported

Event ID CASEID DRUG REC ACT PT
127819441 12781944 Acute kidney injury
127819441 12781944 Decreased appetite
127819441 12781944 Fluid intake reduced
127819441 12781944 Hyperkalaemia
127819441 12781944 Toxicity to various agents

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
127819441 12781944 1 20160607 0
127819441 12781944 2 20160607 0