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
121101072 12110107 2 F 201512 20160729 20160224 20160804 EXP PHHY2016FR022513 NOVARTIS 52.89 YR F Y 0.00000 20160804 OT FR FR

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
121101072 12110107 1 PS DESFERAL DEFEROXAMINE MESYLATE 1 Subcutaneous 3 G, BID 966 G Y 16267 3 G BID
121101072 12110107 2 SS SIKLOS HYDROXYUREA 1 Oral 1000 MG, QD 161000 MG 0 1000 MG TABLET QD
121101072 12110107 3 SS SIKLOS HYDROXYUREA 1 Oral 500 MG, QD 161000 MG 0 500 MG TABLET QD
121101072 12110107 4 SS FERRIPROX DEFERIPRONE 1 Oral 500 MG, TID 241500 MG Y 0 500 MG TABLET TID
121101072 12110107 5 SS AUGMENTIN AMOXICILLINCLAVULANATE POTASSIUM 1 Oral UNK Y 0
121101072 12110107 6 SS TAVANIC LEVOFLOXACIN 1 Oral UNK Y 0
121101072 12110107 7 C LAROXYL AMITRIPTYLINE 1 Oral 40 MG/ML, UNK 0 ORAL SOLUTION
121101072 12110107 8 C PLAQUENIL HYDROXYCHLOROQUINE SULFATE 1 Oral 200 MG, BID 0 200 MG TABLET BID
121101072 12110107 9 C SPECIAFOLDINE FOLIC ACID 1 Oral 5 MG, QD 0 5 MG TABLET QD
121101072 12110107 10 C TOPALGIC LP TRAMADOL 1 Oral 50 MG, TID 0 50 MG SLOW RELEASE TABLET TID
121101072 12110107 11 C LAMALINE ACETAMINOPHENCAFFEINEOPIUM 1 Oral UNK UNK, PRN 0
121101072 12110107 12 C INORIAL BILASTINE 1 Oral 20 MG, UNK 0 20 MG TABLET
121101072 12110107 13 C COVERSYL//PERINDOPRIL ARGININE PERINDOPRIL ARGININE 1 Oral 5 MG, QD 0 5 MG TABLET QD
121101072 12110107 14 C BIPROFENID KETOPROFEN 1 Oral 50 MG (100 MG, 0.5 DF), TID 0 50 MG SLOW RELEASE CAPSULES TID

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
121101072 12110107 1 Sickle cell anaemia
121101072 12110107 2 Sickle cell anaemia
121101072 12110107 4 Product used for unknown indication
121101072 12110107 5 Infection
121101072 12110107 6 Infection
121101072 12110107 7 Product used for unknown indication
121101072 12110107 8 Arthritis
121101072 12110107 9 Product used for unknown indication
121101072 12110107 10 Product used for unknown indication
121101072 12110107 11 Product used for unknown indication
121101072 12110107 12 Product used for unknown indication
121101072 12110107 13 Product used for unknown indication
121101072 12110107 14 Product used for unknown indication

Outcome of event

Event ID CASEID OUTC COD
121101072 12110107 HO

Reactions reported

Event ID CASEID DRUG REC ACT PT
121101072 12110107 Asthenia
121101072 12110107 Epistaxis
121101072 12110107 Pancytopenia

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
121101072 12110107 1 20150721 20151229 0
121101072 12110107 2 20150721 20151229 0
121101072 12110107 3 201602 0
121101072 12110107 4 20150721 20151229 0
121101072 12110107 5 20151127 20151211 0
121101072 12110107 6 20151127 20151211 0
121101072 12110107 8 20150630 0
121101072 12110107 13 20150701 0