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
118159903 11815990 3 F 20151124 20160720 20151209 20160726 EXP US-GLAXOSMITHKLINE-US2015GSK175046 GLAXOSMITHKLINE 72.01 YR F Y 0.00000 20160726 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
118159903 11815990 1 PS ADVAIR HFA FLUTICASONE PROPIONATESALMETEROL XINAFOATE 1 Unknown UNK, U U UNKNOWN 21077
118159903 11815990 2 SS ADVAIR HFA FLUTICASONE PROPIONATESALMETEROL XINAFOATE 1 U 21077

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
118159903 11815990 1 Chronic obstructive pulmonary disease
118159903 11815990 2 Chronic obstructive pulmonary disease

Outcome of event

Event ID CASEID OUTC COD
118159903 11815990 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
118159903 11815990 Dysphonia
118159903 11815990 Speech disorder
118159903 11815990 Throat cancer

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
118159903 11815990 1 2005 0