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
127623561 12762356 1 I 20160730 20160915 20160920 20160920 PER US-GLAXOSMITHKLINE-US2016135487 GLAXOSMITHKLINE 59.46 YR F Y 0.00000 20160920 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
127623561 12762356 1 PS ADVAIR DISKUS FLUTICASONE PROPIONATESALMETEROL XINAFOATE 1 Respiratory (inhalation) 1 PUFF(S), BID UNKNOWN 21077 1 DF INHALATION POWDER BID
127623561 12762356 2 SS ADVAIR DISKUS FLUTICASONE PROPIONATESALMETEROL XINAFOATE 1 21077 INHALATION POWDER
127623561 12762356 3 SS VENTOLIN HFA ALBUTEROL SULFATE 1 Respiratory (inhalation) 2 PUFF(S), PRN XU8P 0 2 DF
127623561 12762356 4 SS VENTOLIN HFA ALBUTEROL SULFATE 1 0
127623561 12762356 5 SS ALCOHOL. ALCOHOL 1 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
127623561 12762356 1 Asthma
127623561 12762356 2 Chronic obstructive pulmonary disease
127623561 12762356 3 Asthma
127623561 12762356 4 Chronic obstructive pulmonary disease

Outcome of event

no results found

Reactions reported

Event ID CASEID DRUG REC ACT PT
127623561 12762356 Anxiety
127623561 12762356 Breath alcohol test positive
127623561 12762356 Dyspnoea

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

no results found

Therapies reported

no results found