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
125236481 12523648 1 I 20160206 20160624 20160704 20160704 EXP GB-MHRA-EYC 00141277 GB-009507513-1606GBR012222 MERCK 71.00 YR M Y 83.91000 KG 20160704 CN 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
125236481 12523648 1 PS SIMVASTATIN. SIMVASTATIN 1 Oral 10 MG, UNK Y U 19766 10 MG TABLET
125236481 12523648 2 SS ATORVASTATIN ATORVASTATIN 1 Oral 40 MG, UNK Y U 0 40 MG
125236481 12523648 3 SS PRAVASTATIN. PRAVASTATIN 1 Oral 10 MG, UNK Y U 0 10 MG
125236481 12523648 4 C BENDROFLUMETHIAZIDE BENDROFLUMETHIAZIDE 1 Oral 2.5 MG, QD U 0 2.5 MG QD
125236481 12523648 5 C FOLIC ACID. FOLIC ACID 1 5 MG, QW U 0 5 MG /wk
125236481 12523648 6 C METHOTREXATE. METHOTREXATE 1 15 MG, QW U 0 15 MG /wk

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
125236481 12523648 1 Blood cholesterol increased
125236481 12523648 2 Blood cholesterol increased
125236481 12523648 3 Blood cholesterol increased

Outcome of event

Event ID CASEID OUTC COD
125236481 12523648 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
125236481 12523648 Abdominal pain
125236481 12523648 Epistaxis
125236481 12523648 Flatulence
125236481 12523648 Gastrointestinal disorder
125236481 12523648 Muscle spasms

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
125236481 12523648 1 20160322 20160324 0
125236481 12523648 2 20160128 20160214 0
125236481 12523648 3 20160510 20160528 0