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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 125593901 | 12559390 | 1 | I | 20160704 | 20160715 | 20160715 | EXP | NZ-ACCORD-042361 | ACCORD | BRUNETTE-LAWREY E, CROFT F. LOSARTAN AND AMLODIPINE OVERDOSE-CASE REPORT OF A PATIENT WITH ANURIC RENAL FAILURE PRIOR TO THE ONSET OF HYPOTENSION. N Z MED J. 2016 MAY 27; 129(1435):84-6. | 54.00 | YR | F | Y | 75.00000 | KG | 20160715 | OT | NZ | NZ |
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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 125593901 | 12559390 | 1 | PS | AMLODIPINE | AMLODIPINE BESYLATE | 1 | 20 TIMES DAILY DOSE AT 18:00 THE PREVIOUS EVENING | 202553 | 200 | MG | |||||||||
| 125593901 | 12559390 | 2 | SS | LOSARTAN. | LOSARTAN | 1 | 27 TIMES MAXIMUM DAILY DOSE AT 18:00 THE PREVIOUS EVENING | 0 | 2700 | G |
Indications of drugs used
| no results found |
Outcome of event
| Event ID | CASEID | OUTC COD |
|---|---|---|
| 125593901 | 12559390 | HO |
Reactions reported
| Event ID | CASEID | DRUG REC ACT | PT |
|---|---|---|---|
| 125593901 | 12559390 | Acute kidney injury | |
| 125593901 | 12559390 | Hypotension | |
| 125593901 | 12559390 | Intentional overdose | |
| 125593901 | 12559390 | Metabolic acidosis | |
| 125593901 | 12559390 | Respiratory failure |
Reporting Sources (this data is often not reported and may therefore be missing here)
| no results found |
Therapies reported
| no results found |