The Safety Rates Drug Report

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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
106747443 10674744 3 F 20141116 20160909 20141224 20160909 EXP PHHO2014DE015834 NOVARTIS 63.87 YR M Y 71.00000 KG 20160909 MD DE DE

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
106747443 10674744 1 PS SERETIDE FLUTICASONE PROPIONATESALMETEROL XINAFOATE 1 Respiratory (inhalation) 1 DF (50/500 ?G), BID 730 DF 0 1 DF BID
106747443 10674744 2 C SPIRIVA TIOTROPIUM BROMIDE MONOHYDRATE 1 Unknown 5 UG (2 X 2.5 1 5 UG) 0 5 UG
106747443 10674744 3 C OLODATEROL OLODATEROL 1 Unknown 5 UG (2 X 2.5 1 5 UG) 0 5 UG
106747443 10674744 4 C SULTANOL ALBUTEROL SULFATE 1 Unknown 0.2 MG, PRN 0 .2 MG

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
106747443 10674744 1 Chronic obstructive pulmonary disease
106747443 10674744 2 Chronic obstructive pulmonary disease
106747443 10674744 3 Chronic obstructive pulmonary disease
106747443 10674744 4 Chronic obstructive pulmonary disease

Outcome of event

Event ID CASEID OUTC COD
106747443 10674744 HO

Reactions reported

Event ID CASEID DRUG REC ACT PT
106747443 10674744 Chronic obstructive pulmonary disease

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
106747443 10674744 1 20131025 20141024 0
106747443 10674744 2 20141025 0
106747443 10674744 3 20141025 0
106747443 10674744 4 20141025 0