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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
127172291 | 12717229 | 1 | I | 201601 | 20160830 | 20160906 | 20160906 | EXP | US-B.I. PHARMACEUTICALS,INC./RIDGEFIELD-2016-BI-56829BP | BOEHRINGER INGELHEIM | 76.47 | YR | M | Y | 0.00000 | 20160906 | 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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
127172291 | 12717229 | 1 | PS | COMBIVENT | ALBUTEROL SULFATEIPRATROPIUM BROMIDE | 1 | Respiratory (inhalation) | DOSE PER APPLICATION: 20 MCG / 100 MCG, INHALATION SPRAY, DAILY DOSE: 80 MCG/400 MCG | 21747 | PRESSURISED INHALATION | QID | ||||||||
127172291 | 12717229 | 2 | SS | SPIRIVA | TIOTROPIUM BROMIDE MONOHYDRATE | 1 | Respiratory (inhalation) | 18 MCG | 21395 | 18 | UG | INHALATION POWDER, HARD CAPSULE | QD | ||||||
127172291 | 12717229 | 3 | C | ALBUTEROL. | ALBUTEROL | 1 | Respiratory (inhalation) | 2 ANZ | 0 | BID |
Indications of drugs used
Event ID | CASEID | INDI DRUG SEQ | INDI PT |
---|---|---|---|
127172291 | 12717229 | 1 | Chronic obstructive pulmonary disease |
127172291 | 12717229 | 2 | Chronic obstructive pulmonary disease |
127172291 | 12717229 | 3 | Chronic obstructive pulmonary disease |
Outcome of event
Event ID | CASEID | OUTC COD |
---|---|---|
127172291 | 12717229 | OT |
Reactions reported
Event ID | CASEID | DRUG REC ACT | PT |
---|---|---|---|
127172291 | 12717229 | Chronic obstructive pulmonary disease | |
127172291 | 12717229 | Lung carcinoma cell type unspecified stage I |
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 |
---|---|---|---|---|---|---|
127172291 | 12717229 | 1 | 2006 | 0 | ||
127172291 | 12717229 | 2 | 2013 | 0 | ||
127172291 | 12717229 | 3 | 2006 | 0 |