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
125849973 12584997 3 F 20160612 20160818 20160722 20160912 PER US-ASTRAZENECA-2016SE78688 ASTRAZENECA 24590.00 DY F Y 62.60000 KG 20160912 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
125849973 12584997 1 PS PULMICORT FLEXHALER BUDESONIDE 1 Respiratory (inhalation) 21949 90 UG INHALATION POWDER BID
125849973 12584997 2 SS PULMICORT FLEXHALER BUDESONIDE 1 Respiratory (inhalation) 90 UG; ONE PUFF, TWICE DAILY, BACM 21949 INHALATION POWDER
125849973 12584997 3 SS METOPROLOL TARTRATE. METOPROLOL TARTRATE 1 Oral 182650 MG 0 50 MG BID
125849973 12584997 4 C SYNTHROID LEVOTHYROXINE SODIUM 1 Oral 0 112 MG QD

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
125849973 12584997 1 Asthma
125849973 12584997 2 Asthma
125849973 12584997 3 Hypertension
125849973 12584997 4 Thyroid disorder

Outcome of event

no results found

Reactions reported

Event ID CASEID DRUG REC ACT PT
125849973 12584997 Asthma
125849973 12584997 Chest discomfort
125849973 12584997 Cough
125849973 12584997 Device malfunction
125849973 12584997 Dyspnoea
125849973 12584997 Rhinorrhoea
125849973 12584997 Upper-airway cough syndrome

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
125849973 12584997 1 201605 0
125849973 12584997 2 20160624 0
125849973 12584997 3 2011 0
125849973 12584997 4 1980 0