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
126088572 12608857 2 F 2014 20160727 20160730 20160819 PER US-ASTRAZENECA-2016SE71139 ASTRAZENECA 78.00 YR M Y 68.00000 KG 20160819 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
126088572 12608857 1 PS SYMBICORT BUDESONIDEFORMOTEROL FUMARATE DIHYDRATE 1 Respiratory (inhalation) 160/4.5 MCG, 1 PUFF TWICE DAILY 21929 BID
126088572 12608857 2 C VENTOLIN ALBUTEROL SULFATE 1 Respiratory (inhalation) 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
126088572 12608857 1 Chronic obstructive pulmonary disease
126088572 12608857 2 Chronic obstructive pulmonary disease

Outcome of event

no results found

Reactions reported

Event ID CASEID DRUG REC ACT PT
126088572 12608857 Condition aggravated
126088572 12608857 Device malfunction
126088572 12608857 Drug dose omission
126088572 12608857 Dyspnoea
126088572 12608857 Malaise
126088572 12608857 Off label use
126088572 12608857 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
126088572 12608857 1 2014 0