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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 127043961 | 12704396 | 1 | I | 201405 | 20160826 | 20160831 | 20160831 | EXP | FR-DSJP-DSE-2016-128862 | DAIICHI | 0.00 | Y | 0.00000 | 20160831 | OT | FR | FR |
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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 127043961 | 12704396 | 1 | PS | Alteis | OLMESARTAN MEDOXOMIL | 1 | Oral | 40 MG, QD | 21286 | 40 | MG | TABLET | QD | ||||||
| 127043961 | 12704396 | 2 | SS | Alteis | OLMESARTAN MEDOXOMIL | 1 | Oral | 20 MG, QD | 21286 | 20 | MG | TABLET | QD | ||||||
| 127043961 | 12704396 | 3 | SS | ALTEISDUO | HYDROCHLOROTHIAZIDEOLMESARTAN MEDOXOMIL | 1 | Oral | UNK | 0 | FILM-COATED TABLET | |||||||||
| 127043961 | 12704396 | 4 | SS | CANDESARTAN | CANDESARTAN | 1 | Oral | 8 MG, QD | 0 | 8 | MG | QD | |||||||
| 127043961 | 12704396 | 5 | SS | ATACAND | CANDESARTAN CILEXETIL | 1 | Oral | 8 MG, QD | 0 | 8 | MG | QD | |||||||
| 127043961 | 12704396 | 6 | SS | ATACAND | CANDESARTAN CILEXETIL | 1 | Oral | 4 MG, QD | 0 | 4 | MG | QD |
Indications of drugs used
| Event ID | CASEID | INDI DRUG SEQ | INDI PT |
|---|---|---|---|
| 127043961 | 12704396 | 1 | Hypertension |
| 127043961 | 12704396 | 3 | Hypertension |
| 127043961 | 12704396 | 4 | Hypertension |
| 127043961 | 12704396 | 5 | Hypertension |
Outcome of event
| Event ID | CASEID | OUTC COD |
|---|---|---|
| 127043961 | 12704396 | OT |
Reactions reported
| Event ID | CASEID | DRUG REC ACT | PT |
|---|---|---|---|
| 127043961 | 12704396 | Asthenia | |
| 127043961 | 12704396 | Diarrhoea | |
| 127043961 | 12704396 | Weight decreased |
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 |
|---|---|---|---|---|---|---|
| 127043961 | 12704396 | 1 | 20121217 | 20130623 | 0 | |
| 127043961 | 12704396 | 2 | 20130725 | 20140406 | 0 | |
| 127043961 | 12704396 | 3 | 20130624 | 20130724 | 0 | |
| 127043961 | 12704396 | 4 | 20140407 | 20151120 | 0 | |
| 127043961 | 12704396 | 5 | 20151121 | 20160311 | 0 | |
| 127043961 | 12704396 | 6 | 20160312 | 20160414 | 0 |