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
82467866 8246786 6 F 20121022 20111116 20121029 EXP PHEH2011US08280 SANDOZ 0.00 M Y 0.00000 20121029 CN US 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
82467866 8246786 1 PS TASIGNA 1 ORAL 150 MG, QID U F0005A 0 150 MG QID
82467866 8246786 2 SS TASIGNA 1 ORAL 300 MG, BID U UNKNOWN 0 300 MG BID
82467866 8246786 3 SS PROMETHAZINE 1 25 MG, Q5H U 84176 25 MG Q5H
82467866 8246786 4 C INSPRA 1 50 MG, BID U 0 50 MG BID
82467866 8246786 5 C NOVOLOG 1 250-300 UNITS PER DAY U 0
82467866 8246786 6 C CATAPRES-TTS-3 2 UNK UKN, UNK U 0 Patch
82467866 8246786 7 C NITROGLYCERIN 1 4 MG, PRN U 0 4 MG
82467866 8246786 8 C ATIVAN 1 1 MG, AS NEEDED U 0 1 MG
82467866 8246786 9 C PERCOCET 1 UNK UKN, UNK U 0
82467866 8246786 10 C RANITIDINE HYDROCHLORIDE 1 1 MG, AS NEEDED U 0 1 MG
82467866 8246786 11 C LOPROX 1 UNK UKN, UNK U 0 Cream

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
82467866 8246786 1 Chronic myeloid leukaemia
82467866 8246786 3 Nausea
82467866 8246786 7 Pain

Outcome of event

Event ID CASEID OUTC COD
82467866 8246786 OT
82467866 8246786 HO

Reactions reported

Event ID CASEID DRUG REC ACT PT
82467866 8246786 Blood pressure increased
82467866 8246786 Chest discomfort
82467866 8246786 Chest pain
82467866 8246786 Coronary artery occlusion
82467866 8246786 Cough
82467866 8246786 Diabetes mellitus
82467866 8246786 Diarrhoea
82467866 8246786 Dizziness
82467866 8246786 Gastric disorder
82467866 8246786 Haemorrhage
82467866 8246786 Headache
82467866 8246786 Herpes zoster
82467866 8246786 Hypertriglyceridaemia
82467866 8246786 Hypopnoea
82467866 8246786 Malaise
82467866 8246786 Nausea
82467866 8246786 Palpitations
82467866 8246786 Pruritus
82467866 8246786 Rhinorrhoea

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
82467866 8246786 1 20120420 0