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
126544993 12654499 3 F 2012 20160920 20160816 20160923 PER US-B.I. PHARMACEUTICALS,INC./RIDGEFIELD-2016-BI-50861BP BOEHRINGER INGELHEIM 0.00 M Y 0.00000 20160923 MD 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
126544993 12654499 1 PS COMBIVENT ALBUTEROL SULFATEIPRATROPIUM BROMIDE 1 Respiratory (inhalation) DOSE PER APPLICATION: 20MCG /100MCG; DAILY DOSE:120MCG/600MCG 504737A,504177B,15L0110,15L0008 21747 PRESSURISED INHALATION
126544993 12654499 2 SS COMBIVENT ALBUTEROL SULFATEIPRATROPIUM BROMIDE 1 Respiratory (inhalation) 2 INHALATIONS OF 18MCG/103MCG; DOSE PER APPLICATION: 36MCG/206MCG; DAILY DOSE: 216MCG/1236MCG FORMUL Y 21747

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
126544993 12654499 1 Chronic obstructive pulmonary disease
126544993 12654499 2 Chronic obstructive pulmonary disease

Outcome of event

no results found

Reactions reported

Event ID CASEID DRUG REC ACT PT
126544993 12654499 Drug ineffective
126544993 12654499 Hypoacusis
126544993 12654499 Memory impairment
126544993 12654499 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
126544993 12654499 1 2011 0
126544993 12654499 2 1996 2011 0