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
125488231 12548823 1 I 201606 20160706 20160712 20160712 EXP US-GLAXOSMITHKLINE-US2016096853 GLAXOSMITHKLINE 0.00 E F Y 0.00000 20160712 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
125488231 12548823 1 PS BREO ELLIPTA FLUTICASONE FUROATEVILANTEROL TRIFENATATE 1 UNK, QD U R757836 204275 INHALATION POWDER QD
125488231 12548823 2 SS BREO ELLIPTA FLUTICASONE FUROATEVILANTEROL TRIFENATATE 1 U 204275 INHALATION POWDER
125488231 12548823 3 SS VENTOLIN HFA ALBUTEROL SULFATE 1 U 0
125488231 12548823 4 SS VENTOLIN HFA ALBUTEROL SULFATE 1 U 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
125488231 12548823 1 Chronic obstructive pulmonary disease
125488231 12548823 2 Asthma
125488231 12548823 3 Chronic obstructive pulmonary disease
125488231 12548823 4 Asthma

Outcome of event

Event ID CASEID OUTC COD
125488231 12548823 HO
125488231 12548823 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
125488231 12548823 Atrial fibrillation
125488231 12548823 Drug dispensing error
125488231 12548823 Drug dose omission
125488231 12548823 Dyspnoea
125488231 12548823 Haematuria
125488231 12548823 Hospitalisation
125488231 12548823 Sluggishness

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
125488231 12548823 1 201606 0