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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
125418671 | 12541867 | 1 | I | 20160627 | 20160708 | 20160708 | PER | US-B.I. PHARMACEUTICALS,INC./RIDGEFIELD-2016-BI-41689BP | BOEHRINGER INGELHEIM | 0.00 | F | Y | 0.00000 | 20160708 | 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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
125418671 | 12541867 | 1 | PS | COMBIVENT | ALBUTEROL SULFATEIPRATROPIUM BROMIDE | 1 | Respiratory (inhalation) | DOSE PER APPLICATION AND DAILY DOSE: 20 MCG / 100 MCG; | 21747 | PRESSURISED INHALATION | QD | ||||||||
125418671 | 12541867 | 2 | C | POTASSIUM | POTASSIUM | 1 | Oral | 0 | TABLET | BID | |||||||||
125418671 | 12541867 | 3 | C | SINGULAIR | MONTELUKAST SODIUM | 1 | Oral | 10 MG | 0 | 10 | MG | TABLET | QD | ||||||
125418671 | 12541867 | 4 | C | ATORVASTATIN | ATORVASTATIN | 1 | Oral | 20 MG | 0 | 20 | MG | TABLET | QD | ||||||
125418671 | 12541867 | 5 | C | ALBUTEROL. | ALBUTEROL | 1 | Respiratory (inhalation) | 0 | NEBULISER LIQUID |
Indications of drugs used
Event ID | CASEID | INDI DRUG SEQ | INDI PT |
---|---|---|---|
125418671 | 12541867 | 1 | Chronic obstructive pulmonary disease |
125418671 | 12541867 | 2 | Product used for unknown indication |
125418671 | 12541867 | 3 | Chronic obstructive pulmonary disease |
125418671 | 12541867 | 4 | Blood cholesterol increased |
125418671 | 12541867 | 5 | Chronic obstructive pulmonary disease |
Outcome of event
no results found |
Reactions reported
Event ID | CASEID | DRUG REC ACT | PT |
---|---|---|---|
125418671 | 12541867 | Hypoacusis | |
125418671 | 12541867 | Increased upper airway secretion | |
125418671 | 12541867 | Throat irritation |
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 |
---|---|---|---|---|---|---|
125418671 | 12541867 | 1 | 2011 | 0 |