Flecainide (Acetate)
Overview
Chemically Minoxidil is identified as 2, 4-diamino-6-piperidinopyrimidine 3-oxide. Oral it is an antihypertensive agent while topical Minoxidil is used for alopecia. Due to its potency and adverse reactions, oral Minoxidil is used mainly for patients with severe, drug-resistant forms of hypertension. Tolerance to prolonged therapy with oral it does not appear to be a problem. Although the oral dosage form was originally approved in October 1979 for use in hypertension, it was first discovered in 1965. Subsequently, in August 1988, a topical formulation was approved for the treatment of alopecia. It has a direct vasodilatory effect on arterial smooth muscle, causing a reduction in peripheral resistance and blood pressure.
Primary Characterstics
Indications
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Pharmacokinetics
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Contraindications
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Side Effects
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Dosage
Flecainide (Acetate)'s dosage details are as follows:
Dose
|
Single Dose
|
Frequency
|
Route
|
Instructions
|
Adult Dosage
|
0 to 2 mg/kg | 1 (1) | 0.8 hourly | IV inf | |
0 to 2 mg/kg | 1 (1) | 2.4 hourly | IV inj | |
0.714 to 2.857 mg/kg | 1.8 (1.7855) | 12 hourly | PO | Individed doses for supra ventricular tachycardia & at rial fibrillation |
Paedriatic Dosage (20kg)
|
100 to 400 mg | 250 (250) | 12 hourly | PO | |
Neonatal Dosage (3kg)
|
| | | | Not recommended in this age group |
High Risk Groups
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Warning / Precautions
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Storage Conditions
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Interference in Pathology
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Brands / Trade Names of
Flecainide (Acetate)
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Manufacturers of
Flecainide (Acetate)
in Pakistan
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