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
126103822 12610382 2 F 2015 20160907 20160801 20160908 EXP US-GLAXOSMITHKLINE-US2016109166 GLAXOSMITHKLINE 66.84 YR 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
126103822 12610382 1 PS ADVAIR DISKUS FLUTICASONE PROPIONATESALMETEROL XINAFOATE 1 Respiratory (inhalation) 1 PUFF(S), BID U 5ZP0753 21077 1 DF INHALATION POWDER BID
126103822 12610382 2 SS VENTOLIN HFA ALBUTEROL SULFATE 1 Respiratory (inhalation) 1 PUFF(S), EVERY 4 HOURS PRN 6ZP6060 0 1 DF
126103822 12610382 3 SS VENTOLIN HFA ALBUTEROL SULFATE 1 0
126103822 12610382 4 C SPIRIVA TIOTROPIUM BROMIDE MONOHYDRATE 1 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
126103822 12610382 1 Asthma
126103822 12610382 2 Asthma
126103822 12610382 3 Pneumonia

Outcome of event

Event ID CASEID OUTC COD
126103822 12610382 OT
126103822 12610382 HO

Reactions reported

Event ID CASEID DRUG REC ACT PT
126103822 12610382 Condition aggravated
126103822 12610382 Dyspnoea
126103822 12610382 Emergency care
126103822 12610382 Nasopharyngitis
126103822 12610382 Pneumonia
126103822 12610382 Respiratory tract infection

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
126103822 12610382 1 2015 0
126103822 12610382 2 2015 0