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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 127811121 | 12781112 | 1 | I | 2014 | 20160920 | 20160926 | 20160926 | EXP | US-DSJP-DSU-2016-131575 | DAIICHI | 0.00 | Y | 0.00000 | 20160926 | MD | 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 127811121 | 12781112 | 1 | PS | TRIBENZOR | AMLODIPINE BESYLATEHYDROCHLOROTHIAZIDEOLMESARTAN MEDOXOMIL | 1 | 40/??/12.5 MG, UNK | Y | 200175 | 1 | DF | FILM-COATED TABLET | |||||||
| 127811121 | 12781112 | 2 | SS | TRIBENZOR | AMLODIPINE BESYLATEHYDROCHLOROTHIAZIDEOLMESARTAN MEDOXOMIL | 1 | UNK | Y | 200175 | FILM-COATED TABLET | |||||||||
| 127811121 | 12781112 | 3 | SS | TRIBENZOR | AMLODIPINE BESYLATEHYDROCHLOROTHIAZIDEOLMESARTAN MEDOXOMIL | 1 | 40/??/12.5 MG, UNK | Y | 200175 | 1 | DF | FILM-COATED TABLET | |||||||
| 127811121 | 12781112 | 4 | SS | TRIBENZOR | AMLODIPINE BESYLATEHYDROCHLOROTHIAZIDEOLMESARTAN MEDOXOMIL | 1 | UNK | Y | 200175 | FILM-COATED TABLET | |||||||||
| 127811121 | 12781112 | 5 | SS | XANAX | ALPRAZOLAM | 1 | UNK | 0 | |||||||||||
| 127811121 | 12781112 | 6 | C | BYSTOLIC | NEBIVOLOL HYDROCHLORIDE | 1 | UNK | 0 |
Indications of drugs used
| Event ID | CASEID | INDI DRUG SEQ | INDI PT |
|---|---|---|---|
| 127811121 | 12781112 | 1 | Hypertension |
| 127811121 | 12781112 | 5 | Product used for unknown indication |
| 127811121 | 12781112 | 6 | Hypertension |
Outcome of event
| Event ID | CASEID | OUTC COD |
|---|---|---|
| 127811121 | 12781112 | OT |
Reactions reported
| Event ID | CASEID | DRUG REC ACT | PT |
|---|---|---|---|
| 127811121 | 12781112 | Burning sensation | |
| 127811121 | 12781112 | Dizziness | |
| 127811121 | 12781112 | Drug ineffective | |
| 127811121 | 12781112 | Fatigue | |
| 127811121 | 12781112 | Insomnia | |
| 127811121 | 12781112 | Malaise | |
| 127811121 | 12781112 | Micturition urgency | |
| 127811121 | 12781112 | Nausea | |
| 127811121 | 12781112 | Neoplasm malignant | |
| 127811121 | 12781112 | Pain | |
| 127811121 | 12781112 | Urine output decreased |
Reporting Sources (this data is often not reported and may therefore be missing here)
| no results found |
Therapies reported
| no results found |