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
127282241 12728224 1 I 20160830 20160907 20160909 20160909 EXP US-GLAXOSMITHKLINE-US2016130803 GLAXOSMITHKLINE 71.48 YR F Y 0.00000 20160909 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
127282241 12728224 1 PS BREO ELLIPTA FLUTICASONE FUROATEVILANTEROL TRIFENATATE 1 Respiratory (inhalation) 1 PUFF(S), QD 2 DF Y R762499 204275 1 DF INHALATION POWDER QD
127282241 12728224 2 SS FLONASE FLUTICASONE PROPIONATE 1 UNK, U U UNKNOWN 0 NASAL SPRAY
127282241 12728224 3 SS FLUTICASONE FLUTICASONEFLUTICASONE PROPIONATE 1 UNK, U U 0
127282241 12728224 4 C ATIVAN LORAZEPAM 1 0
127282241 12728224 5 C DUONEB ALBUTEROL SULFATEIPRATROPIUM BROMIDE 1 0
127282241 12728224 6 C ZOLOFT SERTRALINE HYDROCHLORIDE 1 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
127282241 12728224 1 Chronic obstructive pulmonary disease
127282241 12728224 2 Product used for unknown indication
127282241 12728224 3 Product used for unknown indication

Outcome of event

Event ID CASEID OUTC COD
127282241 12728224 HO
127282241 12728224 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
127282241 12728224 Documented hypersensitivity to administered product
127282241 12728224 Drug hypersensitivity
127282241 12728224 Dyspnoea
127282241 12728224 Pneumonia

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
127282241 12728224 1 20160827 20160829 0