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
127584412 12758441 2 F 200305 20160922 20160919 20160929 PER US-GLAXOSMITHKLINE-US2016GSK135765 GLAXOSMITHKLINE 54.19 YR F Y 0.00000 20160929 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
127584412 12758441 1 PS ADVAIR DISKUS FLUTICASONE PROPIONATESALMETEROL XINAFOATE 1 Respiratory (inhalation) 1 PUFF(S), BID Y U 21077 1 DF INHALATION POWDER BID
127584412 12758441 2 SS SEREVENT DISKUS SALMETEROL XINAFOATE 1 U 0
127584412 12758441 3 SS SYMBICORT BUDESONIDEFORMOTEROL FUMARATE DIHYDRATE 1 U 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
127584412 12758441 1 Asthma

Outcome of event

no results found

Reactions reported

Event ID CASEID DRUG REC ACT PT
127584412 12758441 Adverse drug reaction
127584412 12758441 Dysphonia
127584412 12758441 Feeling abnormal
127584412 12758441 Laryngitis
127584412 12758441 Multiple allergies
127584412 12758441 Psychotic disorder
127584412 12758441 Swelling face

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
127584412 12758441 1 200305 200305 0