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
125322811 12532281 1 I 2015 20160630 20160706 20160706 EXP US-B.I. PHARMACEUTICALS,INC./RIDGEFIELD-2016-BI-43040BP BOEHRINGER INGELHEIM 0.00 F Y 0.00000 20160706 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
125322811 12532281 1 PS SPIRIVA TIOTROPIUM BROMIDE MONOHYDRATE 1 Respiratory (inhalation) 18 MCG 21395 18 UG INHALATION POWDER, HARD CAPSULE QD
125322811 12532281 2 C ADVAIR HFA FLUTICASONE PROPIONATESALMETEROL XINAFOATE 1 Unknown 0
125322811 12532281 3 C PROVENTIL ALBUTEROL 1 Unknown 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
125322811 12532281 1 Chronic obstructive pulmonary disease
125322811 12532281 2 Product used for unknown indication
125322811 12532281 3 Product used for unknown indication

Outcome of event

Event ID CASEID OUTC COD
125322811 12532281 HO

Reactions reported

Event ID CASEID DRUG REC ACT PT
125322811 12532281 Dysphonia
125322811 12532281 Dyspnoea
125322811 12532281 Pneumonia

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
125322811 12532281 1 2004 0