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
104932992 10493299 2 F 20160614 20141002 20160630 EXP US-GLAXOSMITHKLINE-A1082236A GLAXOSMITHKLINE 0.00 M Y 0.00000 20160630 OT 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
104932992 10493299 1 PS ADVAIR DISKUS FLUTICASONE PROPIONATESALMETEROL XINAFOATE 1 Unknown 250/50 MCG, UNKNOWN DOSING UNKNOWN 21077 INHALATION POWDER
104932992 10493299 2 SS ADVAIR DISKUS FLUTICASONE PROPIONATESALMETEROL XINAFOATE 1 21077 INHALATION POWDER
104932992 10493299 3 SS VENTOLIN HFA ALBUTEROL SULFATE 1 Unknown 2 PUFF(S), PRN UNKNOWN 0 2 DF
104932992 10493299 4 SS VENTOLIN HFA ALBUTEROL SULFATE 1 0
104932992 10493299 5 SS ANORO ELLIPTA UMECLIDINIUM BROMIDEVILANTEROL TRIFENATATE 1 Respiratory (inhalation) 1 PUFF(S), QD 0 1 DF INHALATION POWDER QD

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
104932992 10493299 1 Chronic obstructive pulmonary disease
104932992 10493299 2 Emphysema
104932992 10493299 3 Dyspnoea
104932992 10493299 4 Wheezing
104932992 10493299 5 Product used for unknown indication

Outcome of event

no results found

Reactions reported

Event ID CASEID DRUG REC ACT PT
104932992 10493299 Blood pressure increased
104932992 10493299 Treatment noncompliance

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
104932992 10493299 1 20140603 0
104932992 10493299 3 20140603 0
104932992 10493299 5 20140812 0