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
124695782 12469578 2 F 2014 20160713 20160615 20160727 PER US-B.I. PHARMACEUTICALS,INC./RIDGEFIELD-2016-BI-35859BP BOEHRINGER INGELHEIM 0.00 M Y 0.00000 20160727 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
124695782 12469578 1 PS COMBIVENT ALBUTEROL SULFATEIPRATROPIUM BROMIDE 1 Respiratory (inhalation) DOSE PER APPLICATION: 20MCG/100 MCG 504177B,15L0108 21747 PRESSURISED INHALATION
124695782 12469578 2 C ADVAIR HFA FLUTICASONE PROPIONATESALMETEROL XINAFOATE 1 Respiratory (inhalation) 0 BID
124695782 12469578 3 C ZYRTEC CETIRIZINE HYDROCHLORIDE 1 Oral 0 QD

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
124695782 12469578 1 Asthma
124695782 12469578 2 Asthma
124695782 12469578 3 Multiple allergies

Outcome of event

no results found

Reactions reported

Event ID CASEID DRUG REC ACT PT
124695782 12469578 Drug ineffective
124695782 12469578 Off label use
124695782 12469578 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
124695782 12469578 1 2014 0