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
104936273 10493627 3 F 20160907 20141002 20160908 PER US-GLAXOSMITHKLINE-A1086373A GLAXOSMITHKLINE 0.00 F Y 0.00000 20160908 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
104936273 10493627 1 PS ADVAIR DISKUS FLUTICASONE PROPIONATESALMETEROL XINAFOATE 1 Respiratory (inhalation) 1 PUFF(S), BID 6ZP4500 21077 1 DF INHALATION POWDER BID
104936273 10493627 2 SS ADVAIR DISKUS FLUTICASONE PROPIONATESALMETEROL XINAFOATE 1 21077 INHALATION POWDER
104936273 10493627 3 SS VENTOLIN HFA ALBUTEROL SULFATE 1 Respiratory (inhalation) 2 PUFF(S), PRN 6ZP6300 0 2 DF
104936273 10493627 4 SS VENTOLIN HFA ALBUTEROL SULFATE 1 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
104936273 10493627 1 Asthma
104936273 10493627 2 Chronic obstructive pulmonary disease
104936273 10493627 3 Asthma
104936273 10493627 4 Chronic obstructive pulmonary disease

Outcome of event

no results found

Reactions reported

Event ID CASEID DRUG REC ACT PT
104936273 10493627 Device use error
104936273 10493627 Dyspnoea
104936273 10493627 Intentional underdose
104936273 10493627 Nasopharyngitis
104936273 10493627 Sinusitis
104936273 10493627 Stomatitis

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
104936273 10493627 1 20100125 0
104936273 10493627 3 20100125 0