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
125259081 12525908 1 I 20160527 20160628 20160705 20160705 EXP ES-ORION CORPORATION ORION PHARMA-ENTC2016-0354 ORION 84.00 YR M Y 0.00000 20160705 PH ES ES

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
125259081 12525908 1 PS STALEVO CARBIDOPAENTACAPONELEVODOPA 1 Oral STRENGTH: 150/37.5/200 MG Y 0 1 DF
125259081 12525908 2 SS EUCREAS METFORMIN HYDROCHLORIDEVILDAGLIPTIN 1 Oral STRENGTH: 850/50 MG Y 0 1 DF BID
125259081 12525908 3 SS RAMIPRIL. RAMIPRIL 1 Oral Y 0 10 MG
125259081 12525908 4 SS LYRICA PREGABALIN 1 Oral Y 0 150 MG TID
125259081 12525908 5 SS NOVONORM REPAGLINIDE 1 Oral Y 0 1 MG TID
125259081 12525908 6 SS PLETAL CILOSTAZOL 1 Oral Y 0 100 MG BID
125259081 12525908 7 SS ROLPRYNA ROPINIROLE HYDROCHLORIDE 1 Oral Y 0 8 MG

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
125259081 12525908 1 Dementia
125259081 12525908 2 Type 2 diabetes mellitus
125259081 12525908 3 Hypertension
125259081 12525908 5 Type 2 diabetes mellitus
125259081 12525908 7 Dementia

Outcome of event

Event ID CASEID OUTC COD
125259081 12525908 HO
125259081 12525908 LT

Reactions reported

Event ID CASEID DRUG REC ACT PT
125259081 12525908 Atrial fibrillation
125259081 12525908 Chest pain
125259081 12525908 Procedural hypotension
125259081 12525908 Renal impairment

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
125259081 12525908 1 2016 201606 0
125259081 12525908 2 2016 201606 0
125259081 12525908 3 2016 201606 0
125259081 12525908 4 2016 201606 0
125259081 12525908 5 2016 201606 0
125259081 12525908 6 2016 201606 0
125259081 12525908 7 2016 201606 0