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
125323991 12532399 1 I 2013 20160623 20160706 20160706 PER US-B.I. PHARMACEUTICALS,INC./RIDGEFIELD-2016-BI-40856BP BOEHRINGER INGELHEIM 0.00 M 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
125323991 12532399 1 PS COMBIVENT ALBUTEROL SULFATEIPRATROPIUM BROMIDE 1 Unknown DOSE PER APPLICATION: 20 MCG /100 MCG 21747 PRESSURISED INHALATION

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
125323991 12532399 1 Chronic obstructive pulmonary disease

Outcome of event

no results found

Reactions reported

Event ID CASEID DRUG REC ACT PT
125323991 12532399 Drug ineffective

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
125323991 12532399 1 2013 0