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
125856832 12585683 2 F 20160421 20160725 20160801 PER US-ASTRAZENECA-2016SE45032 ASTRAZENECA 0.00 M Y 133.80000 KG 20160801 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
125856832 12585683 1 PS TUDORZA PRESSAIR ACLIDINIUM BROMIDE 1 Respiratory (inhalation) U 202450 400 UG INHALATION POWDER BID
125856832 12585683 2 SS TUDORZA PRESSAIR ACLIDINIUM BROMIDE 1 Respiratory (inhalation) U 202450 400 UG INHALATION POWDER BID
125856832 12585683 3 SS PRILOSEC OMEPRAZOLE MAGNESIUM 1 Oral 0 10 MG QD
125856832 12585683 4 C WATER PILL UNSPECIFIED INGREDIENT 1 0
125856832 12585683 5 C MEDICATIONS FOR HIGH BLOOD PRESSURE 2 0
125856832 12585683 6 C MEDICATIONS FOR HIGH CHOLESTEROL 2 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
125856832 12585683 1 Bronchitis chronic
125856832 12585683 2 Seasonal allergy
125856832 12585683 3 Gastrooesophageal reflux disease
125856832 12585683 5 Hypertension
125856832 12585683 6 Blood cholesterol increased

Outcome of event

no results found

Reactions reported

Event ID CASEID DRUG REC ACT PT
125856832 12585683 Dyspnoea
125856832 12585683 Intentional product misuse
125856832 12585683 Off label use
125856832 12585683 Sleep apnoea syndrome
125856832 12585683 Wheezing

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
125856832 12585683 1 201512 0
125856832 12585683 2 201512 0