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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
127282241 | 12728224 | 1 | I | 20160830 | 20160907 | 20160909 | 20160909 | EXP | US-GLAXOSMITHKLINE-US2016130803 | GLAXOSMITHKLINE | 71.48 | YR | F | Y | 0.00000 | 20160909 | 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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
127282241 | 12728224 | 1 | PS | BREO ELLIPTA | FLUTICASONE FUROATEVILANTEROL TRIFENATATE | 1 | Respiratory (inhalation) | 1 PUFF(S), QD | 2 | DF | Y | R762499 | 204275 | 1 | DF | INHALATION POWDER | QD | ||
127282241 | 12728224 | 2 | SS | FLONASE | FLUTICASONE PROPIONATE | 1 | UNK, U | U | UNKNOWN | 0 | NASAL SPRAY | ||||||||
127282241 | 12728224 | 3 | SS | FLUTICASONE | FLUTICASONEFLUTICASONE PROPIONATE | 1 | UNK, U | U | 0 | ||||||||||
127282241 | 12728224 | 4 | C | ATIVAN | LORAZEPAM | 1 | 0 | ||||||||||||
127282241 | 12728224 | 5 | C | DUONEB | ALBUTEROL SULFATEIPRATROPIUM BROMIDE | 1 | 0 | ||||||||||||
127282241 | 12728224 | 6 | C | ZOLOFT | SERTRALINE HYDROCHLORIDE | 1 | 0 |
Indications of drugs used
Event ID | CASEID | INDI DRUG SEQ | INDI PT |
---|---|---|---|
127282241 | 12728224 | 1 | Chronic obstructive pulmonary disease |
127282241 | 12728224 | 2 | Product used for unknown indication |
127282241 | 12728224 | 3 | Product used for unknown indication |
Outcome of event
Event ID | CASEID | OUTC COD |
---|---|---|
127282241 | 12728224 | HO |
127282241 | 12728224 | OT |
Reactions reported
Event ID | CASEID | DRUG REC ACT | PT |
---|---|---|---|
127282241 | 12728224 | Documented hypersensitivity to administered product | |
127282241 | 12728224 | Drug hypersensitivity | |
127282241 | 12728224 | Dyspnoea | |
127282241 | 12728224 | Pneumonia |
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 |
---|---|---|---|---|---|---|
127282241 | 12728224 | 1 | 20160827 | 20160829 | 0 |