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
125585071 12558507 1 I 20160608 20160608 20160714 20160714 PER US-ASTRAZENECA-2016SE62107 ASTRAZENECA 22548.00 DY F Y 65.80000 KG 20160715 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
125585071 12558507 1 PS PULMICORT FLEXHALER BUDESONIDE 1 Respiratory (inhalation) 90 MCG 2 PUFFS TWICE A DAY 21949 INHALATION POWDER
125585071 12558507 2 SS PULMICORT FLEXHALER BUDESONIDE 1 Respiratory (inhalation) 90 MCG 2 PUFFS TWICE A DAY 21949 INHALATION POWDER
125585071 12558507 3 SS PULMICORT FLEXHALER BUDESONIDE 1 Respiratory (inhalation) 90 MCG 2 PUFFS TWICE A DAY 21949 INHALATION POWDER
125585071 12558507 4 C DIABETES MEDICATION UNSPECIFIED INGREDIENT 1 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
125585071 12558507 1 Nasal congestion
125585071 12558507 2 Cough
125585071 12558507 3 Upper-airway cough syndrome
125585071 12558507 4 Type 2 diabetes mellitus

Outcome of event

no results found

Reactions reported

Event ID CASEID DRUG REC ACT PT
125585071 12558507 Gastrooesophageal reflux disease
125585071 12558507 Intentional product misuse
125585071 12558507 Malaise
125585071 12558507 Product use issue
125585071 12558507 Type 2 diabetes mellitus

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
125585071 12558507 1 20160608 0
125585071 12558507 2 20160608 0
125585071 12558507 3 20160608 0