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
122850592 12285059 2 F 20160404 20160523 20160420 20160707 PER US-ASTRAZENECA-2016SE39369 ASTRAZENECA 31538.00 DY F Y 68.00000 KG 20160707 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
122850592 12285059 1 PS PULMICORT FLEXHALER BUDESONIDE 1 Respiratory (inhalation) 180MCG ONE PUFF TWICE DAILY PAKT 21949 INHALATION POWDER
122850592 12285059 2 SS PULMICORT FLEXHALER BUDESONIDE 1 Respiratory (inhalation) 180MCG ONE PUFF TWICE DAILY PAKT 21949 INHALATION POWDER
122850592 12285059 3 C MEDICATION FOR BLOOD PRESSURE 2 0
122850592 12285059 4 C MEDICATION FOR CHOLESTEROL 2 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
122850592 12285059 1 Asthma
122850592 12285059 2 Dyspnoea
122850592 12285059 3 Hypertension
122850592 12285059 4 Blood cholesterol abnormal

Outcome of event

no results found

Reactions reported

Event ID CASEID DRUG REC ACT PT
122850592 12285059 Dyspnoea
122850592 12285059 Oropharyngeal pain
122850592 12285059 Pain
122850592 12285059 Product quality issue

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
122850592 12285059 1 20160325 0
122850592 12285059 2 20160325 0