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
102078803 10207880 3 F 20160724 20160809 20140530 20160815 EXP US-GLAXOSMITHKLINE-A1063729A GLAXOSMITHKLINE 49.00 YR M Y 0.00000 20160815 OT 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
102078803 10207880 1 SS VENTOLIN ALBUTEROL SULFATE 1 Unknown 90 MCG UNKNOWN DOSING U UNKNOWN 0 90 UG
102078803 10207880 2 PS ADVAIR DISKUS FLUTICASONE PROPIONATESALMETEROL XINAFOATE 1 Unknown 100/50 MCG U UNKNOWN 21077 INHALATION POWDER
102078803 10207880 3 SS VENTOLIN HFA ALBUTEROL SULFATE 1 U UNKNOWN 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
102078803 10207880 1 Respiratory disorder
102078803 10207880 2 Respiratory disorder
102078803 10207880 3 Product used for unknown indication

Outcome of event

Event ID CASEID OUTC COD
102078803 10207880 HO

Reactions reported

Event ID CASEID DRUG REC ACT PT
102078803 10207880 Dyspnoea
102078803 10207880 Emergency care examination

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
102078803 10207880 1 20120731 0
102078803 10207880 2 20120731 0