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
126490811 12649081 1 I 201208 20160811 20160812 20160812 EXP US-B.I. PHARMACEUTICALS,INC./RIDGEFIELD-2016-BI-52838BP BOEHRINGER INGELHEIM 71.31 YR M Y 0.00000 20160812 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
126490811 12649081 1 PS SPIRIVA TIOTROPIUM BROMIDE MONOHYDRATE 1 Respiratory (inhalation) 18 MCG 21395 18 UG INHALATION POWDER, HARD CAPSULE QD
126490811 12649081 2 C ASPIRIN. ASPIRIN 1 Oral 81 MG 0 81 MG TABLET QD
126490811 12649081 3 C POTASSIUM POTASSIUM 1 Oral 2 ANZ 0 TABLET BID

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
126490811 12649081 1 Chronic obstructive pulmonary disease
126490811 12649081 2 Product used for unknown indication
126490811 12649081 3 Pollakiuria

Outcome of event

Event ID CASEID OUTC COD
126490811 12649081 DE

Reactions reported

Event ID CASEID DRUG REC ACT PT
126490811 12649081 Death
126490811 12649081 Fall
126490811 12649081 Therapeutic response unexpected
126490811 12649081 Thrombosis

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
126490811 12649081 1 201001 0