Aldomet

Aldomet

methyldopa

Manufacturer:

Aspen

Distributor:

Zuellig
Full Prescribing Info
Contents
Methyldopa.
Description
Each tablet contains 250 mg of methyldopa.
Action
Antihypertensive.
Aldomet is an effective antihypertensive agent that reduces both supine and standing blood pressure. Symptomatic postural hypotension, exercise hypotension and diurnal blood pressure variations rarely occur. By adjustment of dosage, morning hypotension can be prevented without sacrificing control of afternoon blood pressure.
Methyldopa has no direct effect on cardiac function and usually does not reduce glomerular filtration rate, renal blood flow or filtration fraction. Cardiac output usually is maintained without cardiac acceleration. In some patients, the heart rate is slowed.
Because of relative freedom from adverse effects on kidney function, methyldopa can be of benefit in the control of high blood pressure, even in the presence of renal impairment. It may help arrest or retard the progression of renal function impairment and damage due to sustained elevation of blood pressure.
Normal or elevated plasma renin activity may decrease in the course of methyldopa therapy.
The ability to inhibit dopa decarboxylase and to deplete animal tissues of norepinephrine resides solely in the L-isomer (methyldopa). In man, the antihypertensive activity appears to be due solely to the L-isomer.
Indications/Uses
Hypertension (mild, moderate or severe).
Dosage/Direction for Use
Oral therapy.
General: Methyldopa is largely excreted by the kidney and patients with impaired renal function may respond to smaller doses. Syncope in older patients may be related to an increased sensitivity and advanced arteriosclerotic vascular disease. This may be avoided by lower doses.
Withdrawal of Aldomet is followed by return of hypertension usually within 48 hrs. This is not complicated by an overshoot of blood pressure.
Therapy with Aldomet may be initiated in most patients already on treatment with other antihypertensive agents.
Aldomet may also be used concomitantly with hydrochlorothiazide and amiloride or β-blocking agents eg, timolol maleate.
When methyldopa is given to patients on other antihypertensives, the dose of these agents may need to be adjusted to effect a smooth transition. Terminate these antihypertensive medications gradually if required (see manufacturers' recommendations on stopping these drugs).
Following such previous antihypertensive therapy, the initial dose of Aldomet should be limited to not more than 500 mg daily and increased as required at intervals of not less than 2 days.
Adults: Usual Starting Dose: 250 mg twice or thrice daily in the first 48 hrs. The daily dosage then may be increased or decreased, preferably at intervals of not less than 2 days, until an adequate response is achieved. The maximum recommended daily dosage is 3 g.
When 500 mg of Aldomet is added to 50 mg of hydrochlorothiazide, the 2 agents may be given together once daily.
Many patients experience sedation for 2 or 3 days when therapy with Aldomet is started or when the dose is increased. When increasing the dosage, therefore, it may be desirable to increase the evening dose first.
Children: Initial dosage is based on 10 mg/kg of body weight daily in 2-4 doses. The daily dosage then is increased or decreased until an adequate response is achieved. The maximum dosage is 65 mg/kg or 3 g daily, whichever is less.
Overdosage
Acute overdosage may produce acute hypotension with other responses attributable to brain and gastrointestinal malfunction (excessive sedation, weakness, bradycardia, dizziness, lightheadedness, constipation, distention, flatus, diarrhea, nausea, vomiting).
In the event of overdosage, symptomatic and supportive measures should be employed. When ingestion is recent, gastric lavage or emesis may reduce absorption. When ingestion has been earlier, infusions may be helpful to promote urinary excretion. Otherwise, management includes special attention to cardiac rate and output, blood volume, electrolyte balance, paralytic ileus, urinary function and cerebral activity.
Sympathomimetic drugs (eg, levarterenol, epinephrine, metaraminol bitartrate) may be indicated. Methyldopa is dialyzable.
Contraindications
Hypersensitivity (including hepatic disorders associated with previous methyldopa therapy) to any of the excipients of Aldomet (see Precautions).
Patients with active hepatic disease eg, acute hepatitis and active cirrhosis; on therapy with monoamine oxidase (MAO) inhibitors.
Special Precautions
Acquired hemolytic anemia has occurred rarely in association with methyldopa therapy. Should clinical symptoms indicate the possibility of anemia, hemoglobin and/or hematocrit determinations should be performed. If anemia is present, appropriate laboratory studies should be done to determine if hemolysis is present. Evidence of hemolytic anemia is an indication for discontinuation of the drug. Discontinuation of methyldopa alone, or the initiation of adrenocortical steroids, usually results in a prompt remission of anemia. Rarely, however, fatalities have occurred.
Some patients on continued therapy with methyldopa develop a positive direct Coombs' test. The incidence of positive Coombs' test as reported by different investigators has averaged between 10% and 20%. A positive Coombs' test rarely occurs in the first 6 months of therapy with methyldopa, and if not encountered within 12 months, is unlikely to develop with continued administration. This phenomenon is also dose-related with the lowest incidence occurring in patients receiving ≤1 g of methyldopa/day. Reversal of the positive Coombs' test occurs within weeks to months after discontinuation of the drug.
Should the need for transfusion arise, prior knowledge of a positive Coombs' reaction will aid in evaluation of the crossmatch. Patients with a positive Coombs' test at the time of crossmatch may exhibit an incompatible minor crossmatch. When this occurs, an indirect Coombs' test should be performed. If negative, transfusion with such blood which is otherwise compatible in the major crossmatch may be carried out. However, if positive, the advisability of transfusion with blood compatible in the major crossmatch should be determined by a hematologist or expert in transfusion problems.
Rarely, a reversible reduction of the white blood cell count with a primary effect on the granulocytes has been seen. The granulocyte count returned promptly to normal on discontinuance of the drug. Reversible thrombocytopenia has occurred rarely.
Occasionally, fever has occurred within the first 3 weeks of administration of methyldopa. In some cases, this fever has been associated with eosinophilia or abnormalities in one or more liver function tests. Jaundice, with or without fever, may occur also, with onset usually within the first 2 or 3 months of therapy. In some patients, the findings are consistent with those of cholestasis.
Rare cases of fatal hepatic necrosis have been reported. Liver biopsy performed in several patients with liver dysfunction showed a microscopic focal necrosis compatible with drug hypersensitivity. A determination of hepatic function and a white cell and differential blood count should be done at intervals during the first 6-12 weeks of therapy, or whenever an unexplained fever may occur. If fever, abnormalities in liver function tests or jaundice appear, therapy with methyldopa should be stopped. If related to methyldopa, the temperature and abnormalities in liver function characteristically have reverted to normal when the drug was discontinued. Methyldopa should not be reinstituted in such patients. Methyldopa should be used with caution in patients with a history of previous liver disease or dysfunction.
Patients may require reduced doses of anesthetics when on therapy with Aldomet. If hypotension does occur during anesthesia, it usually can be controlled by vasopressors. The adrenergic receptors remain sensitive during treatment with methyldopa.
Dialysis removes methyldopa; therefore, hypertension may recur after this procedure.
Interference with Laboratory Tests: Methyldopa may interfere with the measurement of urinary uric acid by the phosphotungstate method, serum creatinine by the alkaline picrate method and serum glutamic oxaloacetic transaminase (SGOT) by the colorimetric method. Interference with spectrophotometric methods for SGOT analysis has not been reported.
Since methyldopa will cause fluorescence in urine samples at the same wavelengths as catecholamines, spuriously high concentrations of urinary catecholamines may be reported. This will interfere with the diagnosis of pheochromocytoma.
It is important to recognize this phenomenon before a patient with a possible pheochromocytoma is subjected to surgery. Methyldopa does not interfere with measurement of vanillylmandelic acid (VMA) by those methods which convert VMA to vanillin. Methyldopa is not recommended for the treatment of patients with pheochromocytoma.
Rarely, when urine is exposed to air after voiding, it may darken because of breakdown of methyldopa or its metabolites.
Use in pregnancy: Aldomet has been used under close medical and obstetric supervision for the treatment of hypertension during pregnancy. There was no clinical evidence that Aldomet caused fetal abnormalities or affected the neonate.
Published reports of the use of methyldopa during all trimesters indicate that if this drug is used during pregnancy, the possibility of fetal harm appears remote. In clinical studies, treatment with Aldomet has been associated with an improved fetal outcome. The majority of the women in these studies were in the 3rd trimester when methyldopa therapy was begun.
Methyldopa does cross the placental barrier and appears in cord blood.
Although no obvious teratogenic effects have been reported, the possibility of fetal injury cannot be excluded, and the use of the drug in women who are or may become pregnant requires that anticipated benefits be weighed against possible risks.
Use in lactation: Methyldopa appears in breast milk. Therefore, caution should be exercised if Aldomet is given to a breastfeeding mother.
Use In Pregnancy & Lactation
Use in Pregnancy: Aldomet has been used under close medical and obstetric supervision for the treatment of hypertension during pregnancy. There was no clinical evidence that Aldomet caused fetal abnormalities or affected the neonate.
Published reports of the use of methyldopa during all trimesters indicate that if this drug is used during pregnancy, the possibility of fetal harm appears remote. In clinical studies, treatment with Aldomet has been associated with an improved fetal outcome. The majority of the women in these studies were in the 3rd trimester when methyldopa therapy was begun.
Methyldopa does cross the placental barrier and appears in cord blood.
Although no obvious teratogenic effects have been reported, the possibility of fetal injury cannot be excluded, and the use of the drug in women who are or may become pregnant requires that anticipated benefits be weighed against possible risks.
Use in Lactation: Methyldopa appears in breast milk. Therefore, caution should be exercised if Aldomet is given to a breastfeeding mother.
Side Effects
Sedation, usually transient, may occur during the initial period of therapy or whenever the dose is increased. Headache, asthenia or weakness may be noted as early and transient symptoms.
Significant side effects due to Aldomet have been infrequent and this agent usually is well tolerated.
The following reactions have been reported:
Central Nervous System: Sedation (usually transient), headache, asthenia or weakness, paresthesias, parkinsonism, Bell's palsy, involuntary choreoathetotic movements. Psychic disturbances including nightmares, impaired mental acuity and reversible mild psychoses or depression. Dizziness, lightheadedness and symptoms of cerebrovascular insufficiency (may be due to lowering of blood pressure).
Cardiovascular: Bradycardia, prolonged carotid sinus hypersensitivity, aggravation of angina pectoris. Orthostatic hypotension (decrease daily dosage). Edema (and weight gain) usually relieved by use of a diuretic. (Discontinue methyldopa if edema progresses or signs of heart failure appear.)
Gastrointestinal: Nausea, vomiting, distention, constipation, flatus, diarrhea, colitis, mild dryness of mouth, sore or "black" tongue, pancreatitis, sialoadenitis.
Hepatic: Liver disorders including hepatitis, jaundice, abnormal liver function tests.
Hematologic: Positive Coombs' test, hemolytic anemia, bone marrow depression, leukopenia, granulocytopenia, thrombocytopenia, eosinophilia. Positive tests for antinuclear antibody, LE cells and rheumatoid factor.
Allergic: Drug-related fever and lupus-like syndrome, myocarditis, pericarditis.
Dermatologic: Rash, as in eczema or lichenoid eruption, toxic epidermal necrolysis.
Others: Nasal stuffiness, rise in blood urea nitrogen, breast enlargement, gynecomastia, lactation, hyperprolactinemia, amenorrhea, impotence, decreased libido, mild arthralgia, with or without joint swelling, myalgia.
Drug Interactions
Lithium: When methyldopa and lithium are given concomitantly, the patient should be monitored carefully for symptoms of lithium toxicity.
Other Antihypertensive Drugs: When methyldopa is used in combination with other antihypertensive drugs, potentiation of antihypertensive action may occur. Patients should be followed carefully to detect side reactions or unusual manifestations of drug idiosyncrasy.
Iron: Several studies demonstrate a decrease in the bioavailability of methyldopa when it is ingested with ferrous sulfate or ferrous gluconate. This may adversely affect blood pressure control in patients treated with methyldopa.
Monoamine Oxidase (MAO) Inhibitors: See Contraindications.
Storage
Store at temperatures not exceeding 30°C. Protect from sunlight and excessive heat.
MIMS Class
Other Antihypertensives
ATC Classification
C02AB01 - methyldopa (levorotatory) ; Belongs to the class of methyldopa, centrally-acting antiadrenergic agents. Used in the treatment of hypertension.
Presentation/Packing
Tab 250 mg x 100's, 500's.
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