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
123713072 12371307 2 F 20160513 20160516 20160803 PER US-ASTRAZENECA-2016SE37113 ASTRAZENECA 0.00 F Y 67.10000 KG 20160803 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
123713072 12371307 1 PS SYMBICORT BUDESONIDEFORMOTEROL FUMARATE DIHYDRATE 1 Respiratory (inhalation) 160/4.5 MCG 2 PUFFS TWICE A DAY 3001121C00 21929 BID
123713072 12371307 2 SS SYMBICORT BUDESONIDEFORMOTEROL FUMARATE DIHYDRATE 1 Respiratory (inhalation) 160/4.5 MCG 2 PUFFS TWICE A DAY 3001121C00 21929 BID
123713072 12371307 3 C MULTIVITAMIN VITAMINS 1 DAILY 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
123713072 12371307 1 Cough
123713072 12371307 2 Nasopharyngitis
123713072 12371307 3 Supplementation therapy

Outcome of event

no results found

Reactions reported

Event ID CASEID DRUG REC ACT PT
123713072 12371307 Device malfunction
123713072 12371307 Drug dose omission
123713072 12371307 Feeling abnormal
123713072 12371307 Malaise
123713072 12371307 Off label use
123713072 12371307 Product use 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
123713072 12371307 1 201603 0
123713072 12371307 2 201603 0