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
127029371 12702937 1 I 20160822 20160831 20160831 PER US-GLAXOSMITHKLINE-US2016122196 GLAXOSMITHKLINE 0.00 M Y 0.00000 20160831 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
127029371 12702937 1 PS ADVAIR DISKUS FLUTICASONE PROPIONATESALMETEROL XINAFOATE 1 Respiratory (inhalation) 1 PUFF(S), BID UNKNOWN 21077 1 DF INHALATION POWDER BID
127029371 12702937 2 SS ADVAIR DISKUS FLUTICASONE PROPIONATESALMETEROL XINAFOATE 1 21077 INHALATION POWDER
127029371 12702937 3 SS FLONASE FLUTICASONE PROPIONATE 1 Nasal 2 PUFF(S), PRN UNKNOWN 0 2 DF NASAL SPRAY
127029371 12702937 4 C ATORVASTATIN ATORVASTATIN 1 0
127029371 12702937 5 C LIPITOR ATORVASTATIN CALCIUM 1 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
127029371 12702937 1 Chronic obstructive pulmonary disease
127029371 12702937 2 Asthma
127029371 12702937 3 Sinus disorder

Outcome of event

no results found

Reactions reported

Event ID CASEID DRUG REC ACT PT
127029371 12702937 Anxiety
127029371 12702937 Cough
127029371 12702937 Drug ineffective
127029371 12702937 Heart rate increased
127029371 12702937 Middle insomnia
127029371 12702937 Palpitations
127029371 12702937 Sinus disorder

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

no results found

Therapies reported

no results found