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
118863012 11886301 2 F 2012 20151222 20160104 20160210 PER US-B.I. PHARMACEUTICALS,INC./RIDGEFIELD-2015-BI-71885BP BOEHRINGER INGELHEIM 0.00 M Y 95.25000 KG 20160210 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
118863012 11886301 1 PS COMBIVENT ALBUTEROL SULFATEIPRATROPIUM BROMIDE 1 Respiratory (inhalation) 8 PUF 21747 NEBULISER LIQUID QID
118863012 11886301 2 SS COMBIVENT ALBUTEROL SULFATEIPRATROPIUM BROMIDE 1 Respiratory (inhalation) 4 PUF 21747 PRESSURISED INHALATION QID
118863012 11886301 3 SS SPIRIVA TIOTROPIUM BROMIDE MONOHYDRATE 1 Respiratory (inhalation) 18 MCG 21395 18 UG INHALATION POWDER, HARD CAPSULE QD
118863012 11886301 4 C ADVAIR HFA FLUTICASONE PROPIONATESALMETEROL XINAFOATE 1 Respiratory (inhalation) DOSE PER APPLICATION: 250/50 MCG; DAILY DOSE: 500 / 100 MCG 0 NEBULISER LIQUID BID

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
118863012 11886301 1 Chronic obstructive pulmonary disease
118863012 11886301 3 Chronic obstructive pulmonary disease
118863012 11886301 4 Chronic obstructive pulmonary disease

Outcome of event

no results found

Reactions reported

Event ID CASEID DRUG REC ACT PT
118863012 11886301 Suffocation feeling

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
118863012 11886301 1 2000 2012 0
118863012 11886301 2 2012 0
118863012 11886301 3 2005 201511 0
118863012 11886301 4 2005 0