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
127875211 12787521 1 I 201604 20160923 20160928 20160928 PER US-GLAXOSMITHKLINE-US2016139914 GLAXOSMITHKLINE 48.88 YR F Y 0.00000 20160928 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
127875211 12787521 1 PS FLOVENT DISKUS FLUTICASONE PROPIONATE 1 Oral 2 PUFF(S), BID UB2C 21433 2 DF BID

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
127875211 12787521 1 Eosinophilic oesophagitis

Outcome of event

no results found

Reactions reported

Event ID CASEID DRUG REC ACT PT
127875211 12787521 Drug ineffective
127875211 12787521 Off label use
127875211 12787521 Product cleaning inadequate
127875211 12787521 Therapeutic response unexpected

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
127875211 12787521 1 201604 0