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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
126712491 | 12671249 | 1 | I | 2015 | 20150924 | 20160822 | 20160822 | PER | US-TEVA-597721USA | TEVA | 0.00 | M | Y | 90.70000 | 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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
126712491 | 12671249 | 1 | PS | FEXOFENADINE | FEXOFENADINEFEXOFENADINE HYDROCHLORIDE | 1 | Oral | 180 MILLIGRAM DAILY; | Y | 4MR0247 (43F130) | 76191 | 180 | MG | TABLET | QD | ||||
126712491 | 12671249 | 2 | SS | FEXOFENADINE | FEXOFENADINEFEXOFENADINE HYDROCHLORIDE | 1 | Y | 4MR0247 (43F130) | 76191 | ||||||||||
126712491 | 12671249 | 3 | SS | FEXOFENADINE | FEXOFENADINEFEXOFENADINE HYDROCHLORIDE | 1 | Y | 4MR0247 (43F130) | 76191 | ||||||||||
126712491 | 12671249 | 4 | SS | FEXOFENADINE | FEXOFENADINEFEXOFENADINE HYDROCHLORIDE | 1 | Y | 4MR0247 (43F130) | 76191 | ||||||||||
126712491 | 12671249 | 5 | C | SINGULAIR | MONTELUKAST SODIUM | 1 | 0 | ||||||||||||
126712491 | 12671249 | 6 | C | AMLODIPINE | AMLODIPINE BESYLATE | 1 | 0 | ||||||||||||
126712491 | 12671249 | 7 | C | CRESTOR | ROSUVASTATIN CALCIUM | 1 | 0 | ||||||||||||
126712491 | 12671249 | 8 | C | LEVOTHYROXINE. | LEVOTHYROXINE | 1 | 0 | ||||||||||||
126712491 | 12671249 | 9 | C | ALLERGEN EXTRACTS | 2 | 0 |
Indications of drugs used
Event ID | CASEID | INDI DRUG SEQ | INDI PT |
---|---|---|---|
126712491 | 12671249 | 1 | Hypersensitivity |
126712491 | 12671249 | 2 | Rhinorrhoea |
126712491 | 12671249 | 3 | Eye pruritus |
126712491 | 12671249 | 4 | Lacrimation increased |
Outcome of event
no results found |
Reactions reported
Event ID | CASEID | DRUG REC ACT | PT |
---|---|---|---|
126712491 | 12671249 | Drug administered to patient of inappropriate age | |
126712491 | 12671249 | Dry mouth | |
126712491 | 12671249 | Dry throat | |
126712491 | 12671249 | Mucosal dryness |
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 |
---|---|---|---|---|---|---|
126712491 | 12671249 | 1 | 2015 | 201509 | 0 |