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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 120600243 | 12060024 | 3 | F | 20160829 | 20160210 | 20160901 | EXP | US-GLAXOSMITHKLINE-US2016GSK017885 | GLAXOSMITHKLINE | 0.00 | F | Y | 0.00000 | 20160901 | 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 120600243 | 12060024 | 1 | PS | SEREVENT DISKUS | SALMETEROL XINAFOATE | 1 | UNK | U | UNKNOWN | 20692 | INHALATION POWDER | ||||||||
| 120600243 | 12060024 | 2 | SS | COREG | CARVEDILOL | 1 | 25 MG, UNK | U | UNKNOWN | 0 | 25 | MG | TABLET | ||||||
| 120600243 | 12060024 | 3 | SS | BECONASE AQ | BECLOMETHASONE DIPROPIONATE MONOHYDRATE | 1 | UNK | U | UNKNOWN | 0 | NASAL SPRAY |
Indications of drugs used
| Event ID | CASEID | INDI DRUG SEQ | INDI PT |
|---|---|---|---|
| 120600243 | 12060024 | 1 | Product used for unknown indication |
| 120600243 | 12060024 | 2 | Product used for unknown indication |
| 120600243 | 12060024 | 3 | Product used for unknown indication |
Outcome of event
| Event ID | CASEID | OUTC COD |
|---|---|---|
| 120600243 | 12060024 | OT |
Reactions reported
| Event ID | CASEID | DRUG REC ACT | PT |
|---|---|---|---|
| 120600243 | 12060024 | Macular degeneration |
Reporting Sources (this data is often not reported and may therefore be missing here)
| no results found |
Therapies reported
| no results found |