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
124933494 12493349 4 F 20160803 20160623 20160810 PER PHEH2016US015149 NOVARTIS 0.00 F Y 0.00000 20160810 CN COUNTRY NOT SPECIFIED 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
124933494 12493349 1 PS ENTRESTO SACUBITRILVALSARTAN 1 Oral 200 MG (97/103), BID 207620 200 MG BID
124933494 12493349 2 SS ENTRESTO SACUBITRILVALSARTAN 1 Oral 100 MG (49/51), UNK 207620 100 MG BID
124933494 12493349 3 SS METOPROLOL. METOPROLOL 1 Oral U 0
124933494 12493349 4 SS LIPITOR ATORVASTATIN CALCIUM 1 Oral U 0
124933494 12493349 5 SS MAG OXIDE MAGNESIUM OXIDE 1 Oral U 0
124933494 12493349 6 SS LASIX FUROSEMIDE 1 Oral U 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
124933494 12493349 1 Cardiac failure congestive
124933494 12493349 3 Product used for unknown indication
124933494 12493349 4 Product used for unknown indication
124933494 12493349 5 Product used for unknown indication
124933494 12493349 6 Product used for unknown indication

Outcome of event

no results found

Reactions reported

Event ID CASEID DRUG REC ACT PT
124933494 12493349 Blood potassium increased
124933494 12493349 Hypotension

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

no results found

Therapies reported

no results found