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
125526151 12552615 1 I 201306 20160708 20160713 20160713 EXP US-B.I. PHARMACEUTICALS,INC./RIDGEFIELD-2016-BI-45106BP BOEHRINGER INGELHEIM 64.07 YR F Y 0.00000 20160713 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
125526151 12552615 1 PS SPIRIVA TIOTROPIUM BROMIDE MONOHYDRATE 1 Respiratory (inhalation) 18 MCG 21395 18 UG INHALATION POWDER, HARD CAPSULE QD
125526151 12552615 2 C SYMBICORT BUDESONIDEFORMOTEROL FUMARATE DIHYDRATE 1 Respiratory (inhalation) 2 ANZ 0 BID
125526151 12552615 3 C DALIRESP ROFLUMILAST 1 Oral 1 ANZ 0 TABLET QD

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
125526151 12552615 1 Emphysema
125526151 12552615 2 Emphysema
125526151 12552615 3 Emphysema

Outcome of event

Event ID CASEID OUTC COD
125526151 12552615 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
125526151 12552615 Amnesia
125526151 12552615 Lung neoplasm malignant

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
125526151 12552615 1 2012 0
125526151 12552615 2 2012 0
125526151 12552615 3 201601 0