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
124734542 12473454 2 F 20160612 20160722 20160616 20160727 EXP CN-GLAXOSMITHKLINE-CN2016GSK084081 GLAXOSMITHKLINE 0.00 F Y 0.00000 20160727 CN CN CN

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
124734542 12473454 1 PS SERETIDE FLUTICASONE PROPIONATESALMETEROL XINAFOATE 1 Respiratory (inhalation) 1 PUFF(S), TID 21077 1 DF INHALATION POWDER TID
124734542 12473454 2 SS SERETIDE FLUTICASONE PROPIONATESALMETEROL XINAFOATE 1 Respiratory (inhalation) 1 PUFF(S), BID 21077 1 DF INHALATION POWDER BID
124734542 12473454 3 SS SERETIDE FLUTICASONE PROPIONATESALMETEROL XINAFOATE 1 Respiratory (inhalation) 1 PUFF(S), QD 21077 1 DF INHALATION POWDER QD
124734542 12473454 4 SS SERETIDE FLUTICASONE PROPIONATESALMETEROL XINAFOATE 1 1 PUFF(S), UNK R35U-A 21077 1 DF INHALATION POWDER

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
124734542 12473454 1 Asthma

Outcome of event

Event ID CASEID OUTC COD
124734542 12473454 HO

Reactions reported

Event ID CASEID DRUG REC ACT PT
124734542 12473454 Condition aggravated
124734542 12473454 Drug dose omission
124734542 12473454 Drug ineffective
124734542 12473454 Inappropriate schedule of drug administration
124734542 12473454 Medication error
124734542 12473454 Prescribed overdose
124734542 12473454 Suspected counterfeit product

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
124734542 12473454 4 20160612 0