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 CASE I F COD FOLL SEQ IMAGE EVENT DT MFR DT FDA DT REPT COD MFR NUM MFR SNDR AGE AGE COD GNDR COD E SUB WT WT COD REPT DT OCCP COD DEATH DT TO MFR CONFID REPORTER COUNTRY
5958970 7025964 I 5958970-6 20081031 20081117 EXP 2008ST000243 SANTARUS, INC. 81 YR M N 20081112 MD UNITED KINGDOM

Drug(s) used by person

Event ID DRUG SEQ ROLE COD DRUGNAME VAL VBM ROUTE DOSE VBM DECHAL RECHAL LOT NUM EXP DT NDA NUM
5958970 1010725496 PS ZEGERID 1 Y D 21636
5958970 1010746642 C ISOSORBIDE MONONITRATE 1 21636
5958970 1010746643 C ATENOLOL 1 21636
5958970 1010746644 C ATORVASTATIN CALCIUM 1 21636
5958970 1010746645 C LISINOPRIL 2 21636
5958970 1010746646 SS QUININE 2 21636
5958970 1010746655 C AMLODIPINE 2 21636
5958970 1010746656 C OLMESARTAN 2 21636
5958970 1010746657 C ASPIRIN 1 21636

Indications of drugs used

no results found

Outcome of event

Event ID OUTC COD
5958970 HO
5958970 OT
5958970 RI

Reactions reported

Event ID PT
5958970 ATRIAL FLUTTER
5958970 BLOOD PARATHYROID HORMONE ABNORMAL
5958970 BRADYCARDIA
5958970 FALL
5958970 HYPOCALCAEMIA
5958970 HYPOKALAEMIA
5958970 HYPOMAGNESAEMIA
5958970 HYPOTENSION
5958970 URINARY TRACT INFECTION

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

Event ID RPSR COD
5958970 FGN
5958970 HP
5958970 LIT

Therapies reported

no results found