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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 126713101 | 12671310 | 1 | I | 201604 | 20160425 | 20160822 | 20160822 | PER | US-TEVA-656200USA | TEVA | 76.00 | YR | M | Y | 87.07000 | 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 126713101 | 12671310 | 1 | PS | FEXOFENADINE | FEXOFENADINEFEXOFENADINE HYDROCHLORIDE | 1 | Oral | 180 MILLIGRAM DAILY; | 5FR0219 | 76191 | 180 | MG | TABLET | QD | |||||
| 126713101 | 12671310 | 2 | SS | FEXOFENADINE | FEXOFENADINEFEXOFENADINE HYDROCHLORIDE | 1 | 5FR0219 | 76191 | |||||||||||
| 126713101 | 12671310 | 3 | SS | FEXOFENADINE | FEXOFENADINEFEXOFENADINE HYDROCHLORIDE | 1 | 5FR0219 | 76191 | |||||||||||
| 126713101 | 12671310 | 4 | SS | FEXOFENADINE | FEXOFENADINEFEXOFENADINE HYDROCHLORIDE | 1 | 5FR0219 | 76191 | |||||||||||
| 126713101 | 12671310 | 5 | SS | FEXOFENADINE | FEXOFENADINEFEXOFENADINE HYDROCHLORIDE | 1 | 5FR0219 | 76191 | |||||||||||
| 126713101 | 12671310 | 6 | C | VITAMINS NOS | VITAMINS | 1 | 0 | ||||||||||||
| 126713101 | 12671310 | 7 | C | ANTIHYPERTENSIVES | UNSPECIFIED INGREDIENT | 1 | 0 |
Indications of drugs used
| Event ID | CASEID | INDI DRUG SEQ | INDI PT |
|---|---|---|---|
| 126713101 | 12671310 | 1 | Perennial allergy |
| 126713101 | 12671310 | 2 | Rhinorrhoea |
| 126713101 | 12671310 | 3 | Sneezing |
| 126713101 | 12671310 | 4 | Eye pruritus |
| 126713101 | 12671310 | 5 | Lacrimation increased |
Outcome of event
| no results found |
Reactions reported
| Event ID | CASEID | DRUG REC ACT | PT |
|---|---|---|---|
| 126713101 | 12671310 | Drug administered to patient of inappropriate age | |
| 126713101 | 12671310 | Drug administration error | |
| 126713101 | 12671310 | Drug effect decreased |
Reporting Sources (this data is often not reported and may therefore be missing here)
| no results found |
Therapies reported
| no results found |