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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 122656342 | 12265634 | 2 | F | 20160322 | 20160707 | 20160413 | 20160713 | EXP | FR-DSJP-DSE-2016-112196 | DAIICHI | 0.00 | Y | 0.00000 | 20160713 | MD | 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 122656342 | 12265634 | 1 | PS | OLMETEC 40 mg | OLMESARTAN MEDOXOMIL | 1 | Oral | 40 MG, QD | Y | 21286 | 40 | MG | TABLET | QD | |||||
| 122656342 | 12265634 | 2 | SS | EUCREAS | METFORMIN HYDROCHLORIDEVILDAGLIPTIN | 1 | Oral | 1 DF, BID | 0 | 1 | DF | BID | |||||||
| 122656342 | 12265634 | 3 | SS | KALEORID | POTASSIUM CHLORIDE | 1 | Oral | 1000 MG, QD | 0 | 1000 | MG | PROLONGED-RELEASE TABLET | QD | ||||||
| 122656342 | 12265634 | 4 | SS | TAHOR | ATORVASTATIN CALCIUM | 1 | Oral | 80 MG, QD | 0 | 80 | MG | FILM-COATED TABLET | QD | ||||||
| 122656342 | 12265634 | 5 | C | SELOKEN /00376902/ | METOPROLOL TARTRATE | 1 | Oral | 100 MG, BID | 0 | 100 | MG | TABLET | BID | ||||||
| 122656342 | 12265634 | 6 | C | AMOXICILLIN. | AMOXICILLIN | 1 | UNK | 0 |
Indications of drugs used
| Event ID | CASEID | INDI DRUG SEQ | INDI PT |
|---|---|---|---|
| 122656342 | 12265634 | 1 | Hypertension |
| 122656342 | 12265634 | 2 | Type 2 diabetes mellitus |
| 122656342 | 12265634 | 3 | Hypokalaemia |
| 122656342 | 12265634 | 4 | Dyslipidaemia |
| 122656342 | 12265634 | 5 | Atrial fibrillation |
| 122656342 | 12265634 | 6 | Lung infection |
Outcome of event
| Event ID | CASEID | OUTC COD |
|---|---|---|
| 122656342 | 12265634 | HO |
Reactions reported
| Event ID | CASEID | DRUG REC ACT | PT |
|---|---|---|---|
| 122656342 | 12265634 | Acute kidney injury | |
| 122656342 | 12265634 | Hyperkalaemia | |
| 122656342 | 12265634 | Lactic acidosis |
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 |
|---|---|---|---|---|---|---|
| 122656342 | 12265634 | 1 | 20160322 | 0 | ||
| 122656342 | 12265634 | 2 | 2008 | 20160322 | 0 | |
| 122656342 | 12265634 | 3 | 20160322 | 0 | ||
| 122656342 | 12265634 | 4 | 20160322 | 0 | ||
| 122656342 | 12265634 | 5 | 2013 | 0 | ||
| 122656342 | 12265634 | 6 | 20160315 | 0 |