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
127498811 12749881 1 I 20160822 20160823 20160916 20160916 PER US-ASTRAZENECA-2016SE97915 ASTRAZENECA 46.00 YR F Y 55.30000 KG 20160916 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
127498811 12749881 1 PS RHINOCORT ALLERGY BUDESONIDE 1 Nasal 2 SPRAYS EACH NOSTRIL U U VACY 20746 NASAL SPRAY
127498811 12749881 2 SS RHINOCORT ALLERGY BUDESONIDE 1 Nasal 2 SPRAYS EACH NOSTRIL U U VACY 20746 NASAL SPRAY

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
127498811 12749881 1 Nasal congestion
127498811 12749881 2 Multiple allergies

Outcome of event

no results found

Reactions reported

Event ID CASEID DRUG REC ACT PT
127498811 12749881 Nausea
127498811 12749881 Somnolence

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
127498811 12749881 1 20160822 0
127498811 12749881 2 20160822 0