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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 126816571 | 12681657 | 1 | I | 2015 | 20160816 | 20160824 | 20160824 | EXP | VN-009507513-1608VNM009568 | MERCK | 54.00 | YR | F | Y | 0.00000 | 20160824 | CN | VN | VN |
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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 126816571 | 12681657 | 1 | PS | COZAAR | LOSARTAN POTASSIUM | 1 | Oral | 1 TABLET (50 MG) ONCE A DAY | 20386 | 50 | MG | FILM-COATED TABLET | QD |
Indications of drugs used
| no results found |
Outcome of event
| Event ID | CASEID | OUTC COD |
|---|---|---|
| 126816571 | 12681657 | HO |
Reactions reported
| Event ID | CASEID | DRUG REC ACT | PT |
|---|---|---|---|
| 126816571 | 12681657 | Blood glucose abnormal | |
| 126816571 | 12681657 | Decreased appetite | |
| 126816571 | 12681657 | Feeling abnormal | |
| 126816571 | 12681657 | Hyperglycaemia | |
| 126816571 | 12681657 | Hypoglycaemia | |
| 126816571 | 12681657 | Insomnia | |
| 126816571 | 12681657 | Pallor | |
| 126816571 | 12681657 | 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 |
|---|---|---|---|---|---|---|
| 126816571 | 12681657 | 1 | 20110813 | 0 |