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
125286161 12528616 1 I 20160701 20160705 20160705 EXP SV-GLAXOSMITHKLINE-SV2016GSK095459 GLAXOSMITHKLINE 80.00 YR F Y 0.00000 20160705 CN SV SV

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
125286161 12528616 1 PS Relvar Ellipta FLUTICASONE FUROATEVILANTEROL TRIFENATATE 1 UNK, RELVAR 100/25 Y 204275
125286161 12528616 2 SS SERETIDE FLUTICASONE PROPIONATESALMETEROL XINAFOATE 1 UNK, SERETIDE 50/500 Y 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
125286161 12528616 1 Asthma
125286161 12528616 2 Asthma

Outcome of event

Event ID CASEID OUTC COD
125286161 12528616 HO
125286161 12528616 LT

Reactions reported

Event ID CASEID DRUG REC ACT PT
125286161 12528616 Asthma

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

no results found

Therapies reported

no results found