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
125203524 12520352 4 F 20160611 20160721 20160701 20160729 EXP CN-ASTRAZENECA-2016SE70766 ASTRAZENECA 66.00 YR M Y 0.00000 20160729 CN CN

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
125203524 12520352 1 PS PULMICORT RESPULES BUDESONIDE 1 Respiratory (inhalation) 10 MG U U 20929 1 MG NEBULISER SUSPENSION BID
125203524 12520352 2 SS PULMICORT RESPULES BUDESONIDE 1 Respiratory (inhalation) 10 MG U U 20929 1 MG NEBULISER SUSPENSION BID
125203524 12520352 3 SS PULMICORT RESPULES BUDESONIDE 1 Respiratory (inhalation) 10 MG U U 20929 2 MG NEBULISER SUSPENSION BID
125203524 12520352 4 SS PULMICORT RESPULES BUDESONIDE 1 Respiratory (inhalation) 10 MG U U 20929 2 MG NEBULISER SUSPENSION BID
125203524 12520352 5 SS BRICANYL TERBUTALINE SULFATE 1 Unknown 30 MG Y U 0 5 MG BID
125203524 12520352 6 SS SYMBICORT BUDESONIDEFORMOTEROL FUMARATE DIHYDRATE 1 Respiratory (inhalation) 0 INHALATION POWDER
125203524 12520352 7 C METHYLPREDNISOLONE. METHYLPREDNISOLONE 1 40 MG, IVGTT 0
125203524 12520352 8 C OMEPRAZOLE. OMEPRAZOLE 1 0
125203524 12520352 9 C DEXAMETHASONE. DEXAMETHASONE 1 Intravenous (not otherwise specified) 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
125203524 12520352 1 Heart rate abnormal
125203524 12520352 2 Chronic obstructive pulmonary disease
125203524 12520352 3 Heart rate abnormal
125203524 12520352 4 Chronic obstructive pulmonary disease
125203524 12520352 5 Chronic obstructive pulmonary disease
125203524 12520352 8 Gastritis

Outcome of event

Event ID CASEID OUTC COD
125203524 12520352 OT
125203524 12520352 LT
125203524 12520352 HO

Reactions reported

Event ID CASEID DRUG REC ACT PT
125203524 12520352 Arrhythmia
125203524 12520352 Atrial tachycardia
125203524 12520352 Chest discomfort
125203524 12520352 Confusional state
125203524 12520352 Cyanosis
125203524 12520352 Disorganised speech
125203524 12520352 Drug dose omission
125203524 12520352 Dyskinesia
125203524 12520352 Dyspnoea
125203524 12520352 Oxygen saturation decreased
125203524 12520352 Pulmonary arterial hypertension
125203524 12520352 Rales
125203524 12520352 Respiratory failure
125203524 12520352 Sinus tachycardia
125203524 12520352 Supraventricular extrasystoles
125203524 12520352 Ventricular extrasystoles
125203524 12520352 Wheezing

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
125203524 12520352 1 20160608 20160610 0
125203524 12520352 2 20160608 20160610 0
125203524 12520352 3 20160611 0
125203524 12520352 4 20160611 0
125203524 12520352 5 20160608 20160610 0
125203524 12520352 7 20160608 20160611 0
125203524 12520352 8 20160608 20160611 0
125203524 12520352 9 20160608 20160611 0