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
126605391 12660539 1 I 201607 20160803 20160817 20160817 EXP US-GLAXOSMITHKLINE-US2016112999 GLAXOSMITHKLINE 67.87 YR M Y 0.00000 20160817 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
126605391 12660539 1 PS SEREVENT DISKUS SALMETEROL XINAFOATE 1 Respiratory (inhalation) 1 PUFF(S), BID N U 20692 1 DF BID
126605391 12660539 2 SS ANORO ELLIPTA UMECLIDINIUM BROMIDEVILANTEROL TRIFENATATE 1 Respiratory (inhalation) 1 PUFF(S), 1D 5ZP3448 0 1 DF INHALATION POWDER QD
126605391 12660539 3 SS Albuterol Inhalational powder ALBUTEROL 1 UNK U 0
126605391 12660539 4 C FUROSEMIDE. FUROSEMIDE 1 0
126605391 12660539 5 C POTASSIUM CHLORIDE. POTASSIUM CHLORIDE 1 0
126605391 12660539 6 C SIMVASTATIN. SIMVASTATIN 1 0
126605391 12660539 7 C Warfarin WARFARIN 1 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
126605391 12660539 1 Asthma
126605391 12660539 2 Asthma
126605391 12660539 3 Dyspnoea

Outcome of event

no results found

Reactions reported

Event ID CASEID DRUG REC ACT PT
126605391 12660539 Drug ineffective
126605391 12660539 Dyspnoea

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
126605391 12660539 1 20160721 0
126605391 12660539 2 20160728 0