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
125978012 12597801 2 F 20160622 20160725 20160727 20160921 PER US-ASTRAZENECA-2016SE70877 ASTRAZENECA 20450.00 DY M Y 83.90000 KG 20160921 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
125978012 12597801 1 PS PULMICORT FLEXHALER BUDESONIDE 1 Respiratory (inhalation) D 21949 180 UG INHALATION POWDER BID
125978012 12597801 2 SS PULMICORT FLEXHALER BUDESONIDE 1 Respiratory (inhalation) D PALE 21949 180 UG INHALATION POWDER BID
125978012 12597801 3 C ADVAIR HFA FLUTICASONE PROPIONATESALMETEROL XINAFOATE 1 Respiratory (inhalation) 0
125978012 12597801 4 C VENTOLIN RESCUE INHALER 2 Respiratory (inhalation) 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
125978012 12597801 1 Asthma
125978012 12597801 2 Asthma
125978012 12597801 3 Asthma
125978012 12597801 4 Respiratory disorder

Outcome of event

no results found

Reactions reported

Event ID CASEID DRUG REC ACT PT
125978012 12597801 Chest discomfort
125978012 12597801 Device issue
125978012 12597801 Intentional product misuse

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
125978012 12597801 2 20160622 0