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
125832081 12583208 1 I 20160712 20160722 20160722 EXP US-GLAXOSMITHKLINE-US2016099775 GLAXOSMITHKLINE 0.00 M Y 0.00000 20160722 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
125832081 12583208 1 PS ADVAIR HFA FLUTICASONE PROPIONATESALMETEROL XINAFOATE 1 2 PUFF(S), BID 21254 2 DF BID
125832081 12583208 2 SS ADVAIR HFA FLUTICASONE PROPIONATESALMETEROL XINAFOATE 1 21254
125832081 12583208 3 SS BREO ELLIPTA FLUTICASONE FUROATEVILANTEROL TRIFENATATE 1 1 PUFF(S), QD U 0 1 DF INHALATION POWDER QD
125832081 12583208 4 SS CARVEDILOL. CARVEDILOL 1 UNK U 0
125832081 12583208 5 SS PULMICORT TURBUHALER BUDESONIDE 1 UNK 0
125832081 12583208 6 SS PULMICORT TURBUHALER BUDESONIDE 1 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
125832081 12583208 1 Wheezing
125832081 12583208 2 Asthma
125832081 12583208 3 Product used for unknown indication
125832081 12583208 4 Hypertension
125832081 12583208 5 Wheezing
125832081 12583208 6 Asthma

Outcome of event

Event ID CASEID OUTC COD
125832081 12583208 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
125832081 12583208 Drug ineffective
125832081 12583208 Gastrooesophageal reflux disease
125832081 12583208 Pericardial effusion
125832081 12583208 Productive cough
125832081 12583208 Weight decreased

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
125832081 12583208 1 2015 0
125832081 12583208 3 201602 0
125832081 12583208 5 2015 0