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
126191711 12619171 1 I 2014 20160719 20160803 20160803 PER US-B.I. PHARMACEUTICALS,INC./RIDGEFIELD-2016-BI-47424BP BOEHRINGER INGELHEIM 0.00 F Y 0.00000 20160803 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
126191711 12619171 1 PS COMBIVENT ALBUTEROL SULFATEIPRATROPIUM BROMIDE 1 Respiratory (inhalation) DOSE PER APPLICATION: 20 MCG / 100 MCG; DAILY DOSE-160MCG/800MCG 21747 PRESSURISED INHALATION
126191711 12619171 2 C PAROXETINE. PAROXETINE 1 Oral 10 MG 0 10 MG TABLET QD

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
126191711 12619171 1 Chronic obstructive pulmonary disease
126191711 12619171 2 Depression

Outcome of event

no results found

Reactions reported

Event ID CASEID DRUG REC ACT PT
126191711 12619171 Dyspnoea
126191711 12619171 Incorrect dose administered
126191711 12619171 Pain in extremity
126191711 12619171 Road traffic accident

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
126191711 12619171 1 2014 0