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
121541512 12154151 2 F 2016 20160722 20160307 20160818 PER US-ASTRAZENECA-2016SE20489 ASTRAZENECA 65.00 YR F Y 74.80000 KG 20160819 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
121541512 12154151 1 PS SYMBICORT BUDESONIDEFORMOTEROL FUMARATE DIHYDRATE 1 Respiratory (inhalation) 160/4.5 MCG, 2 PUFFS TWO TIMES A DAY 21929 Q12H
121541512 12154151 2 SS SYMBICORT BUDESONIDEFORMOTEROL FUMARATE DIHYDRATE 1 Respiratory (inhalation) 160/4.5 MCG, 2 PUFFS TWO TIMES A DAY 3001087C00 21929 Q12H
121541512 12154151 3 C HARVONI LEDIPASVIRSOFOSBUVIR 1 Oral 0 90 MG QD

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
121541512 12154151 1 Chronic obstructive pulmonary disease
121541512 12154151 2 Chronic obstructive pulmonary disease
121541512 12154151 3 Hepatitis

Outcome of event

no results found

Reactions reported

Event ID CASEID DRUG REC ACT PT
121541512 12154151 Abdominal discomfort
121541512 12154151 Chest pain
121541512 12154151 Dyspepsia
121541512 12154151 Intentional product misuse
121541512 12154151 Oropharyngeal pain
121541512 12154151 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
121541512 12154151 1 201506 0
121541512 12154151 2 20160224 0
121541512 12154151 3 201601 0