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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
121405824 | 12140582 | 4 | F | 201508 | 20160913 | 20160303 | 20160916 | PER | US-GLAXOSMITHKLINE-US2016028498 | GLAXOSMITHKLINE | 69.10 | YR | F | Y | 0.00000 | 20160916 | 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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
121405824 | 12140582 | 1 | PS | INCRUSE ELLIPTA | UMECLIDINIUM BROMIDE | 1 | Respiratory (inhalation) | 1 PUFF(S), 1D | Y | U | R756735 | 0 | 1 | DF | INHALATION POWDER | QD | |||
121405824 | 12140582 | 2 | SS | ADVAIR DISKUS | FLUTICASONE PROPIONATESALMETEROL XINAFOATE | 1 | UNK, QD (250/50) | U | 5ZP0395 | 0 | INHALATION POWDER | QD | |||||||
121405824 | 12140582 | 3 | SS | SPIRIVA | TIOTROPIUM BROMIDE MONOHYDRATE | 1 | U | 0 | |||||||||||
121405824 | 12140582 | 4 | C | LISINOPRIL. | LISINOPRIL | 1 | 0 | ||||||||||||
121405824 | 12140582 | 5 | C | PROAIR HFA | ALBUTEROL SULFATE | 1 | 0 | ||||||||||||
121405824 | 12140582 | 6 | C | ADVAIR HFA | FLUTICASONE PROPIONATESALMETEROL XINAFOATE | 1 | 0 |
Indications of drugs used
Event ID | CASEID | INDI DRUG SEQ | INDI PT |
---|---|---|---|
121405824 | 12140582 | 1 | Chronic obstructive pulmonary disease |
121405824 | 12140582 | 2 | Chronic obstructive pulmonary disease |
121405824 | 12140582 | 3 | Product used for unknown indication |
Outcome of event
Event ID | CASEID | OUTC COD |
---|---|---|
121405824 | 12140582 | OT |
Reactions reported
Event ID | CASEID | DRUG REC ACT | PT |
---|---|---|---|
121405824 | 12140582 | Biopsy lung | |
121405824 | 12140582 | Incorrect dose administered | |
121405824 | 12140582 | Intentional product use issue | |
121405824 | 12140582 | Lung infection | |
121405824 | 12140582 | Pruritus | |
121405824 | 12140582 | Staphylococcal infection | |
121405824 | 12140582 | Vision blurred |
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 |
---|---|---|---|---|---|---|
121405824 | 12140582 | 1 | 20160224 | 20160226 | 0 |