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
123145572 12314557 2 F 20160627 20160428 20160708 EXP US-GLAXOSMITHKLINE-US2016GSK050305 GLAXOSMITHKLINE 0.00 F Y 0.00000 20160708 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
123145572 12314557 1 PS VENTOLIN HFA ALBUTEROL SULFATE 1 U 20983
123145572 12314557 2 SS ADVAIR DISKUS FLUTICASONE PROPIONATESALMETEROL XINAFOATE 1 U 0 INHALATION POWDER

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
123145572 12314557 1 Chronic obstructive pulmonary disease
123145572 12314557 2 Chronic obstructive pulmonary disease

Outcome of event

no results found

Reactions reported

Event ID CASEID DRUG REC ACT PT
123145572 12314557 Cough
123145572 12314557 Dyspnoea
123145572 12314557 Malaise
123145572 12314557 Rhinorrhoea
123145572 12314557 Therapy change

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

no results found

Therapies reported

no results found