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
100508984 10050898 4 F 20160822 20140401 20160825 EXP US-GLAXOSMITHKLINE-A1008405A GLAXOSMITHKLINE 0.00 F Y 0.00000 20160825 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
100508984 10050898 1 PS ADVAIR DISKUS FLUTICASONE PROPIONATESALMETEROL XINAFOATE 1 250/50 UG, 3-4 TIMES DAILY U 21077 INHALATION POWDER
100508984 10050898 2 SS ADVAIR DISKUS FLUTICASONE PROPIONATESALMETEROL XINAFOATE 1 500/50 UG, MORE THAN 2 TIMES DAILY U 21077 INHALATION POWDER
100508984 10050898 3 SS VENTOLIN ALBUTEROL SULFATE 1 90 MCG AT 3-4 TIMES DAILY U UNKNOWN 0
100508984 10050898 4 SS ADVAIR HFA FLUTICASONE PROPIONATESALMETEROL XINAFOATE 1 1 PUFF(S), QD U 21077 1 DF INHALATION POWDER QD

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
100508984 10050898 1 Asthma
100508984 10050898 3 Asthma
100508984 10050898 4 Product used for unknown indication

Outcome of event

Event ID CASEID OUTC COD
100508984 10050898 HO

Reactions reported

Event ID CASEID DRUG REC ACT PT
100508984 10050898 Anaemia
100508984 10050898 Bronchitis
100508984 10050898 Dyspnoea
100508984 10050898 Intentional underdose
100508984 10050898 Overdose

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
100508984 10050898 1 20090204 0
100508984 10050898 3 20090204 0