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Community data Updated 2 months ago
500 mg
2 x 14
৳7.00

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Same active ingredient — pay up to 56% less

These brands contain the same active ingredient (Methyldopa). Strength and form may differ — confirm substitution with your doctor or pharmacist before switching.

From ৳7.00 (2 x 14)
Available as: 500 mg · 2 x 14 500 mg 500 mg 500 mg

Indications & Uses

Sardopa is indicated for:

Dosage Reference

Reference Information Only

Dosages shown are general references from official sources. Always consult your doctor or pharmacist for personalized dosing.

Adults:

Adults. Initiation of therapy: the usual starting dose of Methyldopa is 250 mg two or three times a day for the first 48 hours. The daily dose may then be increased or decreased, preferably at intervals of not less than two days, until an adequate response is achieved. To minimize sedation, start any dose increase in the evening. When Methyldopa is given to patients already on other antihypertensives, the dose of those agents may need to be adjusted to allow a smooth transition. When Methyldopa is given with antihypertensives other than thiazides, the initial dose of Methyldopa should be limited to 500 mg daily in divided doses; when Methyldopa is added to a thiazide, the thiazide dose need not be changed. Maintenance therapy: the usual daily dose of Methyldopa is 500 mg to 2 g in two to four doses. Although occasional patients have responded to higher doses, the maximum recommended daily dose is 3 g. Tolerance may occasionally develop, usually between the second and third month of therapy. Adding a diuretic or increasing the dose of Methyldopa will frequently restore effective control of blood pressure. A thiazide may be added at any time during Methyldopa therapy and is recommended if therapy has not been started with a thiazide, or if effective control of blood pressure cannot be maintained on 2 g of Methyldopa daily. Methyldopa is largely excreted by the kidney, so patients with impaired renal function may respond to smaller doses. Syncope in older patients may be related to increased sensitivity and advanced arteriosclerotic vascular disease; this may be avoided by using lower doses. Pediatric use: the initial dose is based on 10 mg/kg of body weight daily in two to four doses. The daily dose is then increased or decreased until an adequate response is achieved. The maximum dose is 65 mg/kg or 3 g daily, whichever is less.

Side Effects

Sedation, which is usually temporary, may occur when treatment begins or whenever the dose is increased. Headache, asthenia, or weakness may also appear as early, short-lived symptoms. The following systemic side effects have rarely been reported with the use of Dopamet: angina pectoris, congestive heart failure, orthostatic hypotension, edema or weight gain, bradycardia, pancreatitis, colitis, vomiting, diarrhea, nausea, constipation, dry mouth, hyperprolactinemia, bone marrow depression, leukopenia, granulocytopenia, thrombocytopenia, hemolytic anemia, positive rheumatoid factor, hepatitis, jaundice, myocarditis, pericarditis, vasculitis, eosinophilia, parkinsonism, Bell's palsy, nightmares, reversible mild psychosis or depression, dizziness, lightheadedness, paresthesias, arthralgia, myalgia, nasal stuffiness, rash, amenorrhea, gynecomastia, lactation, and impotence. Significant adverse effects from Dopamet have, however, been infrequent, and the medicine is usually well tolerated.

Cautions & Contraindications

Warnings & Precautions

Use Dopamet with caution in patients who have a history of liver disease or impaired liver function. Some patients taking Dopamet develop clinical oedema (fluid retention) or gain weight; this can usually be controlled with a diuretic. Dopamet should be stopped if the oedema worsens or if signs of heart failure appear. Hypertension has occasionally returned after dialysis in patients receiving Dopamet, because the drug is removed from the body during this procedure. Rarely, involuntary choreoathetotic movements (jerky, writhing movements) have been seen during Dopamet therapy in patients with severe bilateral cerebrovascular disease. If such movements occur, stop treatment.

Contraindications

Methyldopa should not be used in patients who have active liver disease, such as acute hepatitis or active cirrhosis; in those who have previously had a liver disorder linked to Methyldopa treatment; in anyone who is hypersensitive to any component of these products; or in patients currently being treated with monoamine oxidase (MAO) inhibitors.

Drug Interactions

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Last updated: 20 Aug 2026