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
123386793 12338679 3 F 201502 20160711 20160505 20160715 EXP US-GLAXOSMITHKLINE-US2016052273 GLAXOSMITHKLINE 69.01 YR F Y 0.00000 20160715 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
123386793 12338679 1 PS ADVAIR DISKUS FLUTICASONE PROPIONATESALMETEROL XINAFOATE 1 UNK U 5ZP2587 21077 INHALATION POWDER
123386793 12338679 2 SS ADVAIR DISKUS FLUTICASONE PROPIONATESALMETEROL XINAFOATE 1 250/50 MCG U 6ZP4158 21077 INHALATION POWDER
123386793 12338679 3 SS VENTOLIN HFA ALBUTEROL SULFATE 1 Respiratory (inhalation) UNK, U U 4ZP3888 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
123386793 12338679 1 Asthma
123386793 12338679 3 Asthma

Outcome of event

Event ID CASEID OUTC COD
123386793 12338679 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
123386793 12338679 Back disorder
123386793 12338679 Expired product administered
123386793 12338679 Malaise
123386793 12338679 Osteoporosis
123386793 12338679 Physiotherapy
123386793 12338679 Spinal operation

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
123386793 12338679 1 2010 0
123386793 12338679 3 2010 0