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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 125225091 | 12522509 | 1 | I | 20160621 | 20160627 | 20160701 | 20160701 | EXP | US-GLAXOSMITHKLINE-US2016091974 | GLAXOSMITHKLINE | 52.67 | YR | F | Y | 0.00000 | 20160701 | 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 125225091 | 12522509 | 1 | PS | FLOVENT DISKUS | FLUTICASONE PROPIONATE | 1 | Respiratory (inhalation) | UNK UNK, 1D PRN | 5ZP2299 | 20833 | INHALATION POWDER | QD | |||||||
| 125225091 | 12522509 | 2 | SS | VENTOLIN HFA | ALBUTEROL SULFATE | 1 | Respiratory (inhalation) | 2 PUFFS Q6H PRN WHEEZING | 6ZP5161 | 0 | 2 | DF | |||||||
| 125225091 | 12522509 | 3 | SS | ANORO ELLIPTA | UMECLIDINIUM BROMIDEVILANTEROL TRIFENATATE | 1 | UNK UNK, U | U | UNKNOWN | 0 | INHALATION POWDER | ||||||||
| 125225091 | 12522509 | 4 | SS | ALBUTEROL. | ALBUTEROL | 1 | UNK UNK, U | U | UNKNOWN | 0 | NEBULISER SOLUTION | ||||||||
| 125225091 | 12522509 | 5 | C | OXYCODONE | OXYCODONE | 1 | U | 0 | |||||||||||
| 125225091 | 12522509 | 6 | C | XANAX | ALPRAZOLAM | 1 | U | 0 |
Indications of drugs used
| Event ID | CASEID | INDI DRUG SEQ | INDI PT |
|---|---|---|---|
| 125225091 | 12522509 | 1 | Chronic obstructive pulmonary disease |
| 125225091 | 12522509 | 2 | Chronic obstructive pulmonary disease |
| 125225091 | 12522509 | 3 | Product used for unknown indication |
| 125225091 | 12522509 | 4 | Product used for unknown indication |
Outcome of event
| Event ID | CASEID | OUTC COD |
|---|---|---|
| 125225091 | 12522509 | HO |
Reactions reported
| Event ID | CASEID | DRUG REC ACT | PT |
|---|---|---|---|
| 125225091 | 12522509 | Anxiety | |
| 125225091 | 12522509 | Dizziness | |
| 125225091 | 12522509 | Drug dose omission | |
| 125225091 | 12522509 | Dyspnoea | |
| 125225091 | 12522509 | Underdose |
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 |
|---|---|---|---|---|---|---|
| 125225091 | 12522509 | 1 | 201603 | 0 | ||
| 125225091 | 12522509 | 2 | 201603 | 0 |