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
120831552 12083155 2 F 20151031 20160811 20160217 20160819 PER US-ASTRAZENECA-2016SE13627 ASTRAZENECA 19904.00 DY M Y 108.00000 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
120831552 12083155 1 PS SYMBICORT BUDESONIDEFORMOTEROL FUMARATE DIHYDRATE 1 Respiratory (inhalation) 160/4.5 MCG 1-2 PUFFS DAILY U U 21929
120831552 12083155 2 SS SYMBICORT BUDESONIDEFORMOTEROL FUMARATE DIHYDRATE 1 Respiratory (inhalation) 160/4.5 MCG 1-2 PUFFS DAILY U U 21929
120831552 12083155 3 C BENAZEPRIL BENAZEPRIL HYDROCHLORIDE 1 Oral 0 80 MG QD
120831552 12083155 4 C AMOXIK-CLAV 2 Oral 1 TABLET TWICE A DAY 0 TABLET
120831552 12083155 5 C ASPERIN 2 Oral 0 81 MG QD
120831552 12083155 6 C MULTIPLE VITAMIN VITAMINS 1 Oral 1 DAILY 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
120831552 12083155 1 Asthma
120831552 12083155 2 Chronic obstructive pulmonary disease
120831552 12083155 3 Hypertension
120831552 12083155 4 Bronchitis

Outcome of event

no results found

Reactions reported

Event ID CASEID DRUG REC ACT PT
120831552 12083155 Bronchitis
120831552 12083155 Drug dose omission
120831552 12083155 Dyspnoea
120831552 12083155 Off label use

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
120831552 12083155 4 20160203 0