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
125887093 12588709 3 F 201606 20160902 20160725 20160912 PER US-B.I. PHARMACEUTICALS,INC./RIDGEFIELD-2016-BI-45774BP BOEHRINGER INGELHEIM 0.00 M Y 0.00000 20160912 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
125887093 12588709 1 PS COMBIVENT ALBUTEROL SULFATEIPRATROPIUM BROMIDE 1 Respiratory (inhalation) DOSE PER APPLICATION: 18MCG / 103MCG; DAILY DOSE: 72MCG/ 412MCG Y 165580A 21747 INHALATION SOLUTION QID
125887093 12588709 2 SS COMBIVENT ALBUTEROL SULFATEIPRATROPIUM BROMIDE 1 Respiratory (inhalation) DOSE PER APPLICATION: 20MCG /100MCG; DAILY DOSE: 80MCG/ 400MCG 507343 21747 PRESSURISED INHALATION QID

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
125887093 12588709 1 Chronic obstructive pulmonary disease
125887093 12588709 2 Chronic obstructive pulmonary disease

Outcome of event

no results found

Reactions reported

Event ID CASEID DRUG REC ACT PT
125887093 12588709 Drug ineffective
125887093 12588709 Product quality issue

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
125887093 12588709 1 1998 2012 0
125887093 12588709 2 2012 0