Pindolol
Overview
Pindolol is oral, nonselective, ß-receptor antagonist with intrinsic sympathomimetic activity (ISA) (i.e., partial agonist activity). Pindolol is the ß-blocker with the highest degree of ISA and nonselective antagonist qualities. The effect of ISA, as with ß-blockade in general, can be selective or nonselective in nature. The partial agonist potential of Pindolol is greater for ß 2- than ß1-receptors, a characteristic that renders the drug a "vasodilatory" ß-blocker. It was approved by the FDA in September 1982 for the treatment of hypertension. Like other ß-adrenergic antagonists, it competes with adrenergic neurotransmitters (e.g., catecholamines) for binding at sympathetic receptor sites, similar to propranolol.
Primary Characterstics
Indications
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Pharmacokinetics
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Contraindications
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Side Effects
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Dosage
Pindolol's dosage details are as follows:
Dose
|
Single Dose
|
Frequency
|
Route
|
Instructions
|
Adult Dosage
|
10 to 40 mg | 25 (25) | 24 hourly | PO | |
Paedriatic Dosage (20kg)
|
| | | | Not recommended for this age group |
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
Pindolol
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