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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 126713391 | 12671339 | 1 | I | 20160413 | 20160414 | 20160822 | 20160822 | PER | US-TEVA-653813USA | TEVA | 79.05 | YR | F | Y | 62.58000 | KG | 20160822 | 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 126713391 | 12671339 | 1 | PS | FEXOFENADINE | FEXOFENADINEFEXOFENADINE HYDROCHLORIDE | 1 | Oral | Y | 4EE1333 (25F043) | 76191 | 60 | MG | TABLET | ||||||
| 126713391 | 12671339 | 2 | SS | FEXOFENADINE | FEXOFENADINEFEXOFENADINE HYDROCHLORIDE | 1 | Y | 4EE1333 (25F043) | 76191 | ||||||||||
| 126713391 | 12671339 | 3 | C | Vite eyes | 2 | 0 | |||||||||||||
| 126713391 | 12671339 | 4 | C | BIOTIN | BIOTIN | 1 | 0 | ||||||||||||
| 126713391 | 12671339 | 5 | C | VITAMIN D | CHOLECALCIFEROL | 1 | 0 | ||||||||||||
| 126713391 | 12671339 | 6 | C | LISINOPRIL. | LISINOPRIL | 1 | 0 | ||||||||||||
| 126713391 | 12671339 | 7 | C | OMEPRAZOLE. | OMEPRAZOLE | 1 | 0 | ||||||||||||
| 126713391 | 12671339 | 8 | C | ATORVASTATIN | ATORVASTATIN | 1 | 0 |
Indications of drugs used
| Event ID | CASEID | INDI DRUG SEQ | INDI PT |
|---|---|---|---|
| 126713391 | 12671339 | 1 | Rhinorrhoea |
| 126713391 | 12671339 | 2 | Nasopharyngitis |
Outcome of event
| no results found |
Reactions reported
| Event ID | CASEID | DRUG REC ACT | PT |
|---|---|---|---|
| 126713391 | 12671339 | Drug administered to patient of inappropriate age | |
| 126713391 | 12671339 | Expired product administered | |
| 126713391 | 12671339 | Product use issue | |
| 126713391 | 12671339 | Somnolence |
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 |
|---|---|---|---|---|---|---|
| 126713391 | 12671339 | 1 | 20160413 | 20160413 | 0 |