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
121062622 12106262 2 F 2010 20160510 20160223 20160817 PER US-ASTRAZENECA-2016SE15063 ASTRAZENECA 41.00 YR F Y 56.70000 KG 20160817 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
121062622 12106262 1 PS SYMBICORT BUDESONIDEFORMOTEROL FUMARATE DIHYDRATE 1 Respiratory (inhalation) 160 INTERMITTENT U U UNKNOWN 21929
121062622 12106262 2 SS OMEPRAZOLE. OMEPRAZOLE 1 Oral U 0 20 MG QD
121062622 12106262 3 C VENTOLIN ALBUTEROL SULFATE 1 Respiratory (inhalation) INTERMITTENT 0
121062622 12106262 4 C MONOLUKEST SODIUM 2 Oral 0 10 MG QD
121062622 12106262 5 C AZELASTINE HYDROCHLORIDE. AZELASTINE HYDROCHLORIDE 1 Nasal 2 UNK TWO TIMES A DAY 0
121062622 12106262 6 C KETOTIFEN FUMURATE 2 INTERMITTENT 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
121062622 12106262 1 Asthma

Outcome of event

no results found

Reactions reported

Event ID CASEID DRUG REC ACT PT
121062622 12106262 Asthma
121062622 12106262 Barrett's oesophagus
121062622 12106262 Candida infection
121062622 12106262 Coeliac disease
121062622 12106262 Drug dose omission
121062622 12106262 Dyspnoea
121062622 12106262 Hiatus hernia
121062622 12106262 Intentional product misuse
121062622 12106262 Nasopharyngitis
121062622 12106262 Vomiting

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
121062622 12106262 3 20160205 0
121062622 12106262 4 20160205 0
121062622 12106262 5 20160205 0
121062622 12106262 6 20160205 0