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
125832342 12583234 2 F 201507 20160809 20160722 20160815 EXP US-B.I. PHARMACEUTICALS,INC./RIDGEFIELD-2016-BI-47116BP BOEHRINGER INGELHEIM 69.04 YR F Y 74.84000 KG 20160815 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
125832342 12583234 1 PS SPIRIVA TIOTROPIUM BROMIDE MONOHYDRATE 1 Respiratory (inhalation) 5 MCG 21936 2.5 UG PRESSURISED INHALATION BID
125832342 12583234 2 C ADVAIR HFA FLUTICASONE PROPIONATESALMETEROL XINAFOATE 1 Unknown 0
125832342 12583234 3 C ATENOLOL. ATENOLOL 1 Unknown 0
125832342 12583234 4 C GEMFIBROZIL. GEMFIBROZIL 1 Unknown 1200 MG 0 600 MG BID

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
125832342 12583234 1 Chronic obstructive pulmonary disease
125832342 12583234 2 Chronic obstructive pulmonary disease
125832342 12583234 3 Hypertension
125832342 12583234 4 Blood cholesterol increased

Outcome of event

Event ID CASEID OUTC COD
125832342 12583234 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
125832342 12583234 Lung neoplasm malignant
125832342 12583234 Total lung capacity abnormal

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
125832342 12583234 1 201503 0