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
127600141 12760014 1 I 201607 20160831 20160919 20160919 PER US-ASTRAZENECA-2016SE93262 ASTRAZENECA 675.00 MON F Y 88.50000 KG 20160919 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
127600141 12760014 1 PS PULMICORT FLEXHALER BUDESONIDE 1 Respiratory (inhalation) 90.0UG UNKNOWN U U BACN 20441 90 UG INHALATION POWDER
127600141 12760014 2 C SINGULAIR MONTELUKAST SODIUM 1 Oral 0 1 DF TABLET QD
127600141 12760014 3 C VENTOLIN ALBUTEROL SULFATE 1 Respiratory (inhalation) AS REQUIRED 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
127600141 12760014 1 Asthma
127600141 12760014 2 Asthma
127600141 12760014 3 Asthma

Outcome of event

no results found

Reactions reported

Event ID CASEID DRUG REC ACT PT
127600141 12760014 Asthma
127600141 12760014 Circumstance or information capable of leading to medication error
127600141 12760014 Intentional product misuse
127600141 12760014 Lung infection
127600141 12760014 Product packaging quantity issue
127600141 12760014 Product taste abnormal

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
127600141 12760014 1 1996 0