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
125688362 12568836 2 F 20160714 20160719 20160819 PER US-ASTRAZENECA-2016SE74247 ASTRAZENECA 0.00 F Y 56.70000 KG 20160820 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
125688362 12568836 1 PS SYMBICORT BUDESONIDEFORMOTEROL FUMARATE DIHYDRATE 1 Respiratory (inhalation) 160/4.5 MCG 2 PUFFS TWICE PER DAY U U 21929 BID
125688362 12568836 2 SS SYMBICORT BUDESONIDEFORMOTEROL FUMARATE DIHYDRATE 1 Respiratory (inhalation) 160/4.5 MCG 2 PUFFS TWICE PER DAY U U 21929 BID
125688362 12568836 3 SS TOPROL XL METOPROLOL SUCCINATE 1 Oral U U 0 50 MG MODIFIED-RELEASE TABLET QD
125688362 12568836 4 SS TOPROL XL METOPROLOL SUCCINATE 1 Oral U U 0 25 MG MODIFIED-RELEASE TABLET QD
125688362 12568836 5 C ZITHROMAX AZITHROMYCIN DIHYDRATE 1 Oral 0 600 MG QD
125688362 12568836 6 C NORVASC AMLODIPINE BESYLATE 1 Oral 0 10 MG QD
125688362 12568836 7 C SYMTHYROID 2 Oral 0 50 MG QD
125688362 12568836 8 C PREDNISONE. PREDNISONE 1 Oral 0 20 MG QD
125688362 12568836 9 C PREDNISONE. PREDNISONE 1 Oral 0 20 MG QD
125688362 12568836 10 C MELATONIN MELATONIN 1 Oral 0 2 MG QD

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
125688362 12568836 1 Chronic obstructive pulmonary disease
125688362 12568836 2 Bronchitis
125688362 12568836 3 Blood pressure abnormal
125688362 12568836 4 Blood pressure abnormal
125688362 12568836 5 Bronchitis
125688362 12568836 6 Blood pressure abnormal
125688362 12568836 7 Thyroid disorder
125688362 12568836 8 Chronic obstructive pulmonary disease
125688362 12568836 9 Bronchitis
125688362 12568836 10 Sleep disorder

Outcome of event

no results found

Reactions reported

Event ID CASEID DRUG REC ACT PT
125688362 12568836 Cough
125688362 12568836 Device malfunction
125688362 12568836 Insomnia
125688362 12568836 Oropharyngeal pain
125688362 12568836 Product taste abnormal

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
125688362 12568836 1 20160705 0
125688362 12568836 2 20160705 0
125688362 12568836 5 20160705 0
125688362 12568836 8 20160705 0
125688362 12568836 9 20160705 0