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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 127583401 | 12758340 | 1 | I | 20160825 | 20160919 | 20160919 | PER | US-GLAXOSMITHKLINE-US2016134667 | GLAXOSMITHKLINE | 0.00 | F | Y | 0.00000 | 20160919 | 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 127583401 | 12758340 | 1 | PS | FLONASE | FLUTICASONE PROPIONATE | 1 | UNK | U | UNK | 205434 | NASAL SPRAY | ||||||||
| 127583401 | 12758340 | 2 | C | CODEINE COUGH SYRUP | CODEINE | 1 | UNK | U | UNK | 0 |
Indications of drugs used
| Event ID | CASEID | INDI DRUG SEQ | INDI PT |
|---|---|---|---|
| 127583401 | 12758340 | 1 | Product used for unknown indication |
| 127583401 | 12758340 | 2 | Product used for unknown indication |
Outcome of event
| no results found |
Reactions reported
| Event ID | CASEID | DRUG REC ACT | PT |
|---|---|---|---|
| 127583401 | 12758340 | Cough | |
| 127583401 | 12758340 | Drug ineffective | |
| 127583401 | 12758340 | Ear discomfort | |
| 127583401 | 12758340 | Ear pain | |
| 127583401 | 12758340 | Increased viscosity of bronchial secretion | |
| 127583401 | 12758340 | Sinusitis | |
| 127583401 | 12758340 | Sputum discoloured | |
| 127583401 | 12758340 | Viral infection |
Reporting Sources (this data is often not reported and may therefore be missing here)
| no results found |
Therapies reported
| no results found |