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
101631483 10163148 3 F 20160823 20140509 20160825 EXP US-GLAXOSMITHKLINE-A1072489A GLAXOSMITHKLINE 0.00 F Y 0.00000 20160825 MD 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
101631483 10163148 1 PS ADVAIR HFA FLUTICASONE PROPIONATESALMETEROL XINAFOATE 1 UNK, U U 21077 INHALATION POWDER
101631483 10163148 2 SS ADVAIR HFA FLUTICASONE PROPIONATESALMETEROL XINAFOATE 1 Unknown 500/50 MCG UNK, U U UNKNOWN 21077 INHALATION POWDER
101631483 10163148 3 SS VENTOLIN HFA ALBUTEROL SULFATE 1 UNK, U U 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
101631483 10163148 1 Product used for unknown indication
101631483 10163148 3 Product used for unknown indication

Outcome of event

Event ID CASEID OUTC COD
101631483 10163148 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
101631483 10163148 Anxiety
101631483 10163148 Condition aggravated
101631483 10163148 Drug dose omission
101631483 10163148 Ill-defined disorder
101631483 10163148 Memory impairment
101631483 10163148 Mental impairment
101631483 10163148 Treatment noncompliance

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
101631483 10163148 3 20141226 0