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
124450112 12445011 2 F 20160512 20160628 20160607 20160711 EXP US-GLAXOSMITHKLINE-US2016GSK070032 GLAXOSMITHKLINE 81.05 YR Y 0.00000 20160711 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
124450112 12445011 1 PS ADVAIR DISKUS FLUTICASONE PROPIONATESALMETEROL XINAFOATE 1 Respiratory (inhalation) 1 PUFF(S), BID 5ZP2958 21077 1 DF INHALATION POWDER BID
124450112 12445011 2 SS PROAIR HFA ALBUTEROL SULFATE 1 2 PUFF(S), PRN DAA57A 0 2 DF

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
124450112 12445011 1 Chronic obstructive pulmonary disease
124450112 12445011 2 Chronic obstructive pulmonary disease

Outcome of event

no results found

Reactions reported

Event ID CASEID DRUG REC ACT PT
124450112 12445011 Dyspnoea
124450112 12445011 Expired device used
124450112 12445011 Intentional product use issue
124450112 12445011 Medication error
124450112 12445011 Product quality issue

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
124450112 12445011 1 2012 0
124450112 12445011 2 2012 0