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
125589001 12558900 1 I 20160530 20160603 20160715 20160715 PER US-ASTRAZENECA-2016SE60220 ASTRAZENECA 8295.00 DY M Y 122.50000 KG 20160715 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
125589001 12558900 1 PS SYMBICORT BUDESONIDEFORMOTEROL FUMARATE DIHYDRATE 1 Respiratory (inhalation) 160/4.5MCG, 2 PUFFS TWICE DAILY 21929
125589001 12558900 2 SS SYMBICORT BUDESONIDEFORMOTEROL FUMARATE DIHYDRATE 1 Respiratory (inhalation) 160/4.5MCG, 2 PUFFS TWICE DAILY 21929
125589001 12558900 3 C ZYRTEC CETIRIZINE HYDROCHLORIDE 1 Oral 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
125589001 12558900 1 Asthma
125589001 12558900 2 Chronic obstructive pulmonary disease
125589001 12558900 3 Dust allergy

Outcome of event

no results found

Reactions reported

Event ID CASEID DRUG REC ACT PT
125589001 12558900 Dysphonia
125589001 12558900 Intentional product misuse

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
125589001 12558900 1 2015 0
125589001 12558900 2 2015 0
125589001 12558900 3 2008 0