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
127270721 12727072 1 I 20160823 20160909 20160909 PER US-ASTRAZENECA-2016SE91000 ASTRAZENECA 0.00 M Y 96.60000 KG 20160909 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
127270721 12727072 1 PS PULMICORT FLEXHALER BUDESONIDE 1 Respiratory (inhalation) 90 MCG,TWO PUFFS TWICE A DAY 21949 INHALATION POWDER
127270721 12727072 2 SS PULMICORT FLEXHALER BUDESONIDE 1 Respiratory (inhalation) 90 MCG,TWO PUFFS TWICE A DAY 21949 INHALATION POWDER
127270721 12727072 3 SS PULMICORT FLEXHALER BUDESONIDE 1 Respiratory (inhalation) 165 MG 21949 INHALATION POWDER
127270721 12727072 4 SS PULMICORT FLEXHALER BUDESONIDE 1 Respiratory (inhalation) 165 MG 21949 INHALATION POWDER
127270721 12727072 5 C RAMIPRIL. RAMIPRIL 1 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
127270721 12727072 1 Bronchitis
127270721 12727072 2 Hypersensitivity
127270721 12727072 3 Bronchitis
127270721 12727072 4 Hypersensitivity
127270721 12727072 5 Hypertension

Outcome of event

no results found

Reactions reported

Event ID CASEID DRUG REC ACT PT
127270721 12727072 Dyspnoea
127270721 12727072 Intentional product misuse
127270721 12727072 Off label use
127270721 12727072 Product quality issue
127270721 12727072 Product use issue

Reporting Sources (this data is often not reported and may therefore be missing here)

no results found

Therapies reported

no results found