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
125269215 12526921 5 F 20160901 20160705 20160908 PER PHEH2016US016502 NOVARTIS 0.00 M Y 0.00000 20160908 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
125269215 12526921 1 PS GLEEVEC IMATINIB MESYLATE 1 Unknown 400 MG, UNK U F002A, F0028, F0031 21588 400 MG TABLET
125269215 12526921 2 C PRENATAL /00231801/ VITAMINS 1 Unknown U 0
125269215 12526921 3 C BAYER ASPIRIN ASPIRIN 1 Unknown U 0
125269215 12526921 4 C SUPER B COMPLEX /01995301/ CYANOCOBALAMINDEXPANTHENOLNIACINAMIDEPYRIDOXINE HYDROCHLORIDERIBOFLAVIN 5'-PHOSPHATE SODIUMTHIAMINE HYDROCHLORIDEVITAMIN B COMPLEX 1 Unknown U 0
125269215 12526921 5 C SODIUM SODIUM 1 Unknown U 0
125269215 12526921 6 C POTASSIUM POTASSIUM 1 Unknown U 0
125269215 12526921 7 C FOLIC ACID. FOLIC ACID 1 Unknown U 0
125269215 12526921 8 C METOPROLOL SUCCINATE. METOPROLOL SUCCINATE 1 Unknown U 0 EXTENDED RELEASE TABLET
125269215 12526921 9 C PRAVASTATIN. PRAVASTATIN 1 Unknown U 0
125269215 12526921 10 C NAPROXEN. NAPROXEN 1 Unknown U 0
125269215 12526921 11 C TRAMADOL. TRAMADOL 1 Unknown U 0
125269215 12526921 12 C TRAZODONE TRAZODONE HYDROCHLORIDE 1 Unknown U 0
125269215 12526921 13 C SILDENAFIL. SILDENAFIL 1 Unknown U 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
125269215 12526921 1 Product used for unknown indication
125269215 12526921 2 Product used for unknown indication
125269215 12526921 3 Product used for unknown indication
125269215 12526921 4 Product used for unknown indication
125269215 12526921 5 Product used for unknown indication
125269215 12526921 6 Product used for unknown indication
125269215 12526921 7 Product used for unknown indication
125269215 12526921 8 Product used for unknown indication
125269215 12526921 9 Product used for unknown indication
125269215 12526921 10 Product used for unknown indication
125269215 12526921 11 Product used for unknown indication
125269215 12526921 12 Product used for unknown indication
125269215 12526921 13 Product used for unknown indication

Outcome of event

no results found

Reactions reported

Event ID CASEID DRUG REC ACT PT
125269215 12526921 Blood disorder
125269215 12526921 Fatigue
125269215 12526921 Product quality issue

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

no results found

Therapies reported

no results found