The Safety Rates Drug Report

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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
103790912 10379091 2 F 201310 20160620 20140812 20160630 EXP US-GLAXOSMITHKLINE-A1083873A GLAXOSMITHKLINE 71.69 YR F Y 0.00000 20160630 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
103790912 10379091 1 PS ADVAIR HFA FLUTICASONE PROPIONATESALMETEROL XINAFOATE 1 Respiratory (inhalation) 250/50 UNKNOWN 21077 1 DF INHALATION POWDER BID
103790912 10379091 2 SS BREO ELLIPTA FLUTICASONE FUROATEVILANTEROL TRIFENATATE 1 Respiratory (inhalation) 1 PUFF(S), 1D R658029 0 1 DF INHALATION POWDER QD
103790912 10379091 3 SS BREO ELLIPTA FLUTICASONE FUROATEVILANTEROL TRIFENATATE 1 1 PUFF(S), 1D R713285 0 1 DF INHALATION POWDER QD
103790912 10379091 4 SS ANORO ELLIPTA UMECLIDINIUM BROMIDEVILANTEROL TRIFENATATE 1 Respiratory (inhalation) UNK, 1D R749798 0 INHALATION POWDER QD
103790912 10379091 5 SS IPRATROPIUM BROMIDE + SALBUTAMOL SULPHATE ALBUTEROL SULFATEIPRATROPIUM BROMIDE 1 Respiratory (inhalation) UNK 5021 0
103790912 10379091 6 SS PROAIR HFA ALBUTEROL SULFATE 1 Unknown 0
103790912 10379091 7 SS CPAP DEVICE 1 Unknown 0
103790912 10379091 8 C Calcium CALCIUM 1 0
103790912 10379091 9 C Ipratropium IPRATROPIUM 1 0 NEBULISER SOLUTION
103790912 10379091 10 C PRAVASTATIN PRAVASTATINPRAVASTATIN SODIUM 1 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
103790912 10379091 1 Chronic obstructive pulmonary disease
103790912 10379091 2 Chronic obstructive pulmonary disease
103790912 10379091 4 Chronic obstructive pulmonary disease
103790912 10379091 5 Chronic obstructive pulmonary disease
103790912 10379091 7 Sleep apnoea syndrome

Outcome of event

Event ID CASEID OUTC COD
103790912 10379091 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
103790912 10379091 Chest discomfort
103790912 10379091 Cough
103790912 10379091 Drug dose omission
103790912 10379091 Drug ineffective
103790912 10379091 Dyspnoea
103790912 10379091 Eye haemorrhage
103790912 10379091 Fungal infection
103790912 10379091 Malaise
103790912 10379091 Middle insomnia
103790912 10379091 Pneumothorax
103790912 10379091 Sleep apnoea syndrome
103790912 10379091 Therapeutic response unexpected
103790912 10379091 Unevaluable event
103790912 10379091 Weight increased

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
103790912 10379091 1 2014 0
103790912 10379091 2 2014 201602 0
103790912 10379091 4 201602 0
103790912 10379091 5 2007 0