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
127665981 12766598 1 I 2011 20160913 20160921 20160921 EXP US-B.I. PHARMACEUTICALS,INC./RIDGEFIELD-2016-BI-59987BP BOEHRINGER INGELHEIM 0.00 F Y 0.00000 20160921 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
127665981 12766598 1 PS COMBIVENT ALBUTEROL SULFATEIPRATROPIUM BROMIDE 1 Respiratory (inhalation) STRENGTH AND DOSE PER APPLICATION: 20MCG / 100 MCG; DAILY DOSE: 2 INHALATION SPRAY 4 TIME PER DAY N 21747 PRESSURISED INHALATION
127665981 12766598 2 SS COMBIVENT ALBUTEROL SULFATEIPRATROPIUM BROMIDE 1 Respiratory (inhalation) STRENGTH AND DOSE PER APPLICATION: 20MCG/100 MCG, DAILY DOSE: 2 INHALATION SPRAY 2 TIME PER AS REQUI N 21747 PRESSURISED INHALATION

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
127665981 12766598 1 Chronic obstructive pulmonary disease

Outcome of event

Event ID CASEID OUTC COD
127665981 12766598 HO

Reactions reported

Event ID CASEID DRUG REC ACT PT
127665981 12766598 Malaise
127665981 12766598 Medication error
127665981 12766598 Renal failure
127665981 12766598 Upper respiratory tract infection

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
127665981 12766598 1 2011 2015 0
127665981 12766598 2 2015 0