Aldomet
Noun | 1. | Aldomet - antihypertensive drug (trade name Aldomet) used in the treatment of high blood pressure |
单词 | aldomet | |||
释义 | Aldomet
AldometAldomet[al´do-met]methyldopamethyldopate hydrochloridePharmacologic class: Centrally acting antiadrenergic Therapeutic class: Antihypertensive Pregnancy risk category B ActionStimulates CNS alpha-adrenergic receptors, decreasing sympathetic stimulation to heart and blood vessels. Also reduces arterial pressure and plasma renin. AvailabilityInjection: 50 mg/ml in 5- and 10-ml vials Oral suspension (contains bisulfites): 250 mg/5 ml Tablets: 125 mg, 250 mg, 500 mg Indications and dosages➣ Hypertension Adults: 250 mg P.O. two to three times daily for 2 days (not to exceed 500 mg/day in divided doses if used with other agents); may increase q 2 days as needed. Usual maintenance dosage is 500 mg to 2 g/day (not to exceed 3 g/day) P.O. in two to four divided doses or 250 to 500 mg I.V. q 6 hours (up to 1 g q 6 hours). Children: 10 mg/kg/day (300 mg/m2/day) P.O. in two to four divided doses. May increase q 2 days up to 65 mg/kg/day (2 g/m2/day), or 3 g/day in divided doses (whichever is lower) or 5 to 10 mg/kg I.V. q 6 hours; up to 65 mg/kg/day (2 g/m2/day), or 3 g/day in divided doses (whichever is lower). Contraindications• Hypersensitivity to drug or its components • Pheochromocytoma • Active hepatic disease or history of methyldopa-associated hepatic disorders • MAO inhibitor use within past 14 days PrecautionsUse cautiously in: • heart failure, edema, hemolytic anemia, hypotension, severe bilateral cerebrovascular disease • dialysis patients • elderly patients • pregnant or breastfeeding patients. AdministrationSee Don't give within 14 days of MAO inhibitors. • To prepare I.V. infusion, add prescribed dosage to 100 ml 5% dextrose injection. Or administer in 5% dextrose injection in a concentration of 100 mg/10 ml. Give each dose over 30 to 60 minutes. • Dilute and administer ADD-Vantage vials containing 50 mg/ml according to manufacturer's instructions. See Don't stop drug therapy abruptly. Adverse reactionsCNS: headache, asthenia, weakness, dizziness, sedation, decreased mental acuity, depression, paresthesia, parkinsonism, Bell's palsy, involuntary choreoathetotic movements CV: bradycardia, edema, orthostatic hypotension, myocarditis EENT: nasal congestion GI: nausea, vomiting, diarrhea, constipation, abdominal distention, colitis, dry mouth, sialadenitis, sore or black tongue, pancreatitis GU: breast enlargement, gynecomastia, failure to ejaculate, erectile dysfunction Hematologic: eosinophilia, hemolytic anemia Hepatic: hepatitis Other: fever InteractionsDrug-drug. Adrenergics, MAO inhibitors: excessive sympathetic stimulation Amphetamines, barbiturates, nonsteroidal anti-inflammatory drugs, phenothiazines, tricyclic antidepressants: decreased antihypertensive effect Anesthestics, antihypertensives, nitrates: additive hypotension Ferrous gluconate, ferrous sulfate: decreased methyldopa blood level Haloperidol: increased haloperidol effects, increased risk of psychoses Levodopa: additive hypotension and CNS toxicity Lithium: increased risk of lithium toxicity Nonselective beta-adrenergic blockers: paradoxical hypertension Tolbutamide: increased tolbutamide effects Drug-diagnostic tests. Alanine aminotransferase, alkaline phosphatase, aspartate aminotransferase, bilirubin, blood urea nitrogen, creatinine, potassium, prolactin, sodium, uric acid: increased levels Direct Coombs' test: positive result Liver function tests: abnormal results Prothrombin time: prolonged Drug-herbs. Capsicum: reduced antihypertensive effects Drug-behaviors. Alcohol use: increased hypotension Patient monitoring• Obtain direct Coombs' test before therapy starts and 6 and 12 months later. • Monitor periodic blood counts to detect adverse hematologic reactions. • Monitor liver function tests and check for signs and symptoms of hepatic dysfunction (particularly during first 6 to 12 weeks of therapy). • Check for edema or weight gain to help determine if diuretic should be added to regimen. • Monitor blood pressure. Drug tolerance may occur during second and third months of therapy. Patient teaching• Tell patient that sedation usually occurs when therapy starts and during dosage titration. To lessen this effect, advise him to begin dosage titration in evening. See Tell patient not to stop taking drug abruptly. See Instruct patient to report fever, yellowing of skin or eyes, fatigue, abdominal pain, flulike symptoms, swelling, or significant weight gain. • Inform patient that urine may darken after exposure to air. • Advise patient to move slowly when changing position, to avoid dizziness from sudden blood pressure decrease. • Caution patient to avoid driving and other hazardous activities until effects of drug are known or dosage titration is completed. • As appropriate, review all other significant and life-threatening adverse reactions and interactions, especially those related to the drugs, tests, herbs, and behaviors mentioned above. Aldomet(ăl′də-mĕt′)AldometA brand name for METHYLDOPA.Aldomet
Synonyms for Aldomet
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