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
126603171 12660317 1 I 20160803 20160817 20160817 EXP PL-ASTRAZENECA-2016SE84391 ASTRAZENECA 51.00 YR M Y 0.00000 20160817 OT PL PL

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
126603171 12660317 1 PS BUDESONIDE, FORMOTEROL FUMARATE BUDESONIDEFORMOTEROL FUMARATE DIHYDRATE 1 Respiratory (inhalation) 320 UG AND 9 UG RESPECTIVELY TWICE A DAY. U 21929 INHALATION POWDER
126603171 12660317 2 SS THEOPHYLLINE THEOPHYLLINE ANHYDROUS 1 Unknown U 0 300 MG QD
126603171 12660317 3 C MONTELUKAST MONTELUKAST SODIUM 1 0 10 MG QD
126603171 12660317 4 C METHYLOPREDNISOLONE 2 0 4 MG QD
126603171 12660317 5 C PREDNISONE. PREDNISONE 1 Oral 30.0MG UNKNOWN 0 30 MG

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
126603171 12660317 4 Asthma prophylaxis
126603171 12660317 5 Asthma prophylaxis

Outcome of event

Event ID CASEID OUTC COD
126603171 12660317 HO

Reactions reported

Event ID CASEID DRUG REC ACT PT
126603171 12660317 Aspergilloma
126603171 12660317 Cataract
126603171 12660317 Dyspnoea
126603171 12660317 Ischaemic stroke
126603171 12660317 Lumbar vertebral fracture
126603171 12660317 Osteoporosis
126603171 12660317 Productive cough
126603171 12660317 Thoracic vertebral fracture
126603171 12660317 Wheezing

Reporting Sources (this data is often not reported and may therefore be missing here)

no results found

Therapies reported

no results found