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
125290331 12529033 1 I 20160619 20160619 20160705 20160705 PER US-B.I. PHARMACEUTICALS,INC./RIDGEFIELD-2016-BI-39994BP BOEHRINGER INGELHEIM 0.00 F Y 0.00000 20160705 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
125290331 12529033 1 PS SPIRIVA TIOTROPIUM BROMIDE MONOHYDRATE 1 Respiratory (inhalation) 18 MCG U 21395 18 UG INHALATION POWDER, HARD CAPSULE QD
125290331 12529033 2 SS SPIRIVA TIOTROPIUM BROMIDE MONOHYDRATE 1 Oral 18 MCG U 21395 18 UG INHALATION POWDER, HARD CAPSULE QD

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
125290331 12529033 1 Chronic obstructive pulmonary disease

Outcome of event

no results found

Reactions reported

Event ID CASEID DRUG REC ACT PT
125290331 12529033 Incorrect route of drug administration
125290331 12529033 Malaise

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
125290331 12529033 2 20160619 20160619 0