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
126591121 12659112 1 I 20160803 20160809 20160817 20160817 EXP BR-GLAXOSMITHKLINE-BR2016GSK116062 GLAXOSMITHKLINE 4.38 YR F Y 17.00000 KG 20160817 CN BR BR

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
126591121 12659112 1 PS SERETIDE FLUTICASONE PROPIONATESALMETEROL XINAFOATE 1 Respiratory (inhalation) 1 PUFF(S), BID 21254 1 DF OROMUCOSAL SPRAY BID

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
126591121 12659112 1 Asthma

Outcome of event

Event ID CASEID OUTC COD
126591121 12659112 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
126591121 12659112 Asthmatic crisis
126591121 12659112 Respiratory disorder

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
126591121 12659112 1 201511 0