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
127239703 12723970 3 F 20160927 20160908 20160928 EXP US-B.I. PHARMACEUTICALS,INC./RIDGEFIELD-2016-BI-58443BP BOEHRINGER INGELHEIM 0.00 F Y 0.00000 20160928 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
127239703 12723970 1 PS COMBIVENT ALBUTEROL SULFATEIPRATROPIUM BROMIDE 1 Respiratory (inhalation) FORMULATION: INHALATION AEROSOL; DOSE PER APPLICATION: 18 MCG/103 MCG; DAILY DOSE: 108 MCG/618 MCG U 507871B 21747
127239703 12723970 2 SS SPIRIVA TIOTROPIUM BROMIDE MONOHYDRATE 1 Respiratory (inhalation) 18 MCG U 602373A 21395 18 UG INHALATION POWDER, HARD CAPSULE QD

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
127239703 12723970 1 Product used for unknown indication
127239703 12723970 2 Product used for unknown indication

Outcome of event

Event ID CASEID OUTC COD
127239703 12723970 HO

Reactions reported

Event ID CASEID DRUG REC ACT PT
127239703 12723970 Unevaluable event

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
127239703 12723970 1 2013 0
127239703 12723970 2 2013 0