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
125897321 12589732 1 I 2015 20160526 20160725 20160725 PER US-ASTRAZENECA-2016SE57830 ASTRAZENECA 79.00 YR F Y 71.70000 KG 20160725 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
125897321 12589732 1 PS SYMBICORT BUDESONIDEFORMOTEROL FUMARATE DIHYDRATE 1 Respiratory (inhalation) 160/4.5 UG, UNKNOWN DOSE AND FREQUENCY UNKNOWN Y Y 21929
125897321 12589732 2 SS SYMBICORT BUDESONIDEFORMOTEROL FUMARATE DIHYDRATE 1 Respiratory (inhalation) 80/4.5 UG, TWO PUFFS TWO TIMES A DAY UNKNOWN Y Y 21929 BID
125897321 12589732 3 SS SYMBICORT BUDESONIDEFORMOTEROL FUMARATE DIHYDRATE 1 Respiratory (inhalation) UNKNOWN Y Y 21929
125897321 12589732 4 C ATROVENT IPRATROPIUM BROMIDE 1 Respiratory (inhalation) EVERY 4 HOURS DURING THE DAY 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
125897321 12589732 1 Bronchiectasis
125897321 12589732 2 Bronchiectasis
125897321 12589732 3 Bronchiectasis

Outcome of event

no results found

Reactions reported

Event ID CASEID DRUG REC ACT PT
125897321 12589732 Lung disorder
125897321 12589732 Muscle spasms
125897321 12589732 Pneumonia
125897321 12589732 Weight decreased
125897321 12589732 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
125897321 12589732 1 2015 0
125897321 12589732 2 2015 2015 0
125897321 12589732 3 2016 0