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
126103661 12610366 1 I 20100913 20160728 20160801 20160801 EXP US-GLAXOSMITHKLINE-US2016109846 GLAXOSMITHKLINE 69.44 YR M Y 0.00000 20160801 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
126103661 12610366 1 PS FLOVENT HFA FLUTICASONE PROPIONATE 1 Respiratory (inhalation) 2 PUFF(S), BID U KB7K 21433 2 DF BID
126103661 12610366 2 SS SEREVENT DISKUS SALMETEROL XINAFOATE 1 Respiratory (inhalation) 1 PUFF(S), BID U 5ZP2002 0 1 DF INHALATION POWDER BID
126103661 12610366 3 SS INCRUSE ELLIPTA UMECLIDINIUM BROMIDE 1 Respiratory (inhalation) 1 PUFF(S), 1D U R747429 0 1 DF INHALATION POWDER QD
126103661 12610366 4 C PREDNISONE. PREDNISONE 1 0
126103661 12610366 5 C AMLODIPINE AMLODIPINE BESYLATE 1 0
126103661 12610366 6 C MONTELUKAST SODIUM. MONTELUKAST SODIUM 1 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
126103661 12610366 1 Asthma
126103661 12610366 2 Asthma
126103661 12610366 3 Asthma

Outcome of event

Event ID CASEID OUTC COD
126103661 12610366 OT
126103661 12610366 HO

Reactions reported

Event ID CASEID DRUG REC ACT PT
126103661 12610366 Colostomy
126103661 12610366 Dyspnoea
126103661 12610366 Intestinal obstruction
126103661 12610366 Plasma cell myeloma

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
126103661 12610366 1 2011 0
126103661 12610366 2 2011 0
126103661 12610366 3 201607 0