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
118409183 11840918 3 F 20160202 20151216 20160210 EXP US-GLAXOSMITHKLINE-US2015GSK176851 GLAXOSMITHKLINE 0.00 M Y 0.00000 20160210 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
118409183 11840918 1 PS ADVAIR DISKUS FLUTICASONE PROPIONATESALMETEROL XINAFOATE 1 UNK 5ZP0903 21077 INHALATION POWDER

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
118409183 11840918 1 Product used for unknown indication

Outcome of event

no results found

Reactions reported

Event ID CASEID DRUG REC ACT PT
118409183 11840918 Drug ineffective
118409183 11840918 Inhalation therapy
118409183 11840918 Product physical consistency issue
118409183 11840918 Product quality issue

Reporting Sources (this data is often not reported and may therefore be missing here)

no results found

Therapies reported

no results found