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
127979081 12797908 1 I 20160926 20160930 20160930 EXP BR-GLAXOSMITHKLINE-BR2016GSK142328 GLAXOSMITHKLINE 0.00 F Y 0.00000 20160930 CN BR BR

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
127979081 12797908 1 PS SERETIDE FLUTICASONE PROPIONATESALMETEROL XINAFOATE 1 Respiratory (inhalation) 2 PUFF(S), QD 21077 2 DF INHALATION POWDER QD
127979081 12797908 2 C SELOZOK (METOPROLOL SUCCINATE) 2 U U 0
127979081 12797908 3 C CARVEDILOL. CARVEDILOL 1 U U 0
127979081 12797908 4 C PREDNISONE. PREDNISONE 1 25 MG, UNK U U 0 25 MG
127979081 12797908 5 C PURAN LEVOTHYROXINE SODIUM 1 75 MG, QD U U 0 75 MG QD

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
127979081 12797908 1 Asthma
127979081 12797908 2 Cardiac disorder
127979081 12797908 3 Cardiac disorder
127979081 12797908 4 Bronchial disorder
127979081 12797908 5 Hyperthyroidism

Outcome of event

Event ID CASEID OUTC COD
127979081 12797908 OT
127979081 12797908 HO

Reactions reported

Event ID CASEID DRUG REC ACT PT
127979081 12797908 Angiopathy
127979081 12797908 Aortic calcification
127979081 12797908 Blood pressure fluctuation
127979081 12797908 Deafness
127979081 12797908 Dizziness
127979081 12797908 Dyspnoea
127979081 12797908 Fatigue
127979081 12797908 Hand deformity
127979081 12797908 Hypertension
127979081 12797908 Ischaemic stroke
127979081 12797908 Off label use
127979081 12797908 Osteoarthritis
127979081 12797908 Pain

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

no results found

Therapies reported

no results found