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
126300101 12630010 1 I 201510 20160801 20160808 20160808 EXP US-B.I. PHARMACEUTICALS,INC./RIDGEFIELD-2016-BI-50393BP BOEHRINGER INGELHEIM 63.14 YR F Y 0.00000 20160808 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
126300101 12630010 1 PS COMBIVENT ALBUTEROL SULFATEIPRATROPIUM BROMIDE 1 Respiratory (inhalation) FORMULATION: INHALATION SPRAY; DOSE PER APPLICATION: 20 MCG / 100 MCG; DAILY DOSE: 80 MCG / 400 MCG 502317A 21747 PRESSURISED INHALATION QID
126300101 12630010 2 C ADVAIR HFA FLUTICASONE PROPIONATESALMETEROL XINAFOATE 1 Respiratory (inhalation) 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
126300101 12630010 1 Chronic obstructive pulmonary disease
126300101 12630010 2 Product used for unknown indication

Outcome of event

Event ID CASEID OUTC COD
126300101 12630010 HO

Reactions reported

Event ID CASEID DRUG REC ACT PT
126300101 12630010 Chronic obstructive pulmonary disease
126300101 12630010 Intra-abdominal haematoma
126300101 12630010 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
126300101 12630010 1 2011 0