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
125893801 12589380 1 I 2016 20160712 20160725 20160725 PER US-B.I. PHARMACEUTICALS,INC./RIDGEFIELD-2016-BI-45793BP BOEHRINGER INGELHEIM 0.00 M Y 0.00000 20160725 PH 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
125893801 12589380 1 PS COMBIVENT ALBUTEROL SULFATEIPRATROPIUM BROMIDE 1 Respiratory (inhalation) 4 ANZ 21747 PRESSURISED INHALATION QD
125893801 12589380 2 C ALBUTEROL. ALBUTEROL 1 Respiratory (inhalation) 8 ANZ 0 PRESSURISED INHALATION
125893801 12589380 3 C DUONEB ALBUTEROL SULFATEIPRATROPIUM BROMIDE 1 Respiratory (inhalation) 4 ANZ 0 ORAL SOLUTION

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
125893801 12589380 1 Chronic obstructive pulmonary disease
125893801 12589380 2 Product used for unknown indication
125893801 12589380 3 Product used for unknown indication

Outcome of event

no results found

Reactions reported

Event ID CASEID DRUG REC ACT PT
125893801 12589380 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
125893801 12589380 1 2013 0