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
898048717 8980487 17 F 201106 20160825 20121221 20160901 EXP PHHY2012CA117568 NOVARTIS 62.83 YR F Y 0.00000 20160901 CN COUNTRY NOT SPECIFIED CA

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
898048717 8980487 1 PS GLEEVEC IMATINIB MESYLATE 1 Oral 400 MG, QD 423600 MG 21588 400 MG QD
898048717 8980487 2 SS GLEEVEC IMATINIB MESYLATE 1 Oral 400 MG, QD 423600 MG 21588 400 MG QD
898048717 8980487 3 C PROLIA DENOSUMAB 1 Unknown UNK U 0
898048717 8980487 4 C FOSAMAX ALENDRONATE SODIUM 1 Unknown UNK 0
898048717 8980487 5 C VITAMIN D CHOLECALCIFEROL 1 Unknown 1000 IU, BID (AT LUNCH AND BEDTIME) U 0 1000 IU BID
898048717 8980487 6 C CALCIUM CALCIUM 1 Unknown 500 MG, BID (AT LUNCH AND BEDTIME) U 0 500 MG BID
898048717 8980487 7 C SYNTHROID LEVOTHYROXINE SODIUM 1 Unknown U 0
898048717 8980487 8 C CORTISONE CORTISONEHYDROCORTISONE 1 Unknown U 0
898048717 8980487 9 C PENICILLIN /02215301/ PENICILLIN 1 Unknown UNK U 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
898048717 8980487 1 Gastrointestinal stromal tumour
898048717 8980487 3 Product used for unknown indication
898048717 8980487 4 Product used for unknown indication
898048717 8980487 5 Product used for unknown indication
898048717 8980487 6 Product used for unknown indication
898048717 8980487 7 Product used for unknown indication
898048717 8980487 8 Product used for unknown indication
898048717 8980487 9 Prophylaxis

Outcome of event

Event ID CASEID OUTC COD
898048717 8980487 HO
898048717 8980487 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
898048717 8980487 Anaemia
898048717 8980487 Arthritis
898048717 8980487 Asthma
898048717 8980487 Bladder disorder
898048717 8980487 Burning sensation
898048717 8980487 Cystitis radiation
898048717 8980487 Dizziness
898048717 8980487 Dry eye
898048717 8980487 Dyspnoea
898048717 8980487 Dysuria
898048717 8980487 Epistaxis
898048717 8980487 Fluid retention
898048717 8980487 Haematuria
898048717 8980487 Haemoptysis
898048717 8980487 Haemorrhage urinary tract
898048717 8980487 Immune system disorder
898048717 8980487 Lung infection
898048717 8980487 Migraine with aura
898048717 8980487 Nausea
898048717 8980487 Pain in extremity
898048717 8980487 Pollakiuria
898048717 8980487 Productive cough
898048717 8980487 Pulmonary mass
898048717 8980487 Pyrexia
898048717 8980487 Secretion discharge
898048717 8980487 Tooth infection
898048717 8980487 Urinary bladder haemorrhage
898048717 8980487 Urinary tract infection
898048717 8980487 Vision blurred
898048717 8980487 Vomiting
898048717 8980487 White blood cell count decreased

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
898048717 8980487 1 20100818 20130711 0
898048717 8980487 2 20130726 0
898048717 8980487 3 201405 0
898048717 8980487 4 201405 0
898048717 8980487 9 20150602 0