Benazepril (HCl)
Benazepril (HCl) is an angeotensin converting enzyme inhibitor (ACEI). Benazepril (HCl) is a prodrug, converted into benazeprilat which is the active form of the drug. It lowers systemic vascular resistance and mean diastolic, and systolic blood pressure in various hypertensive states. ACE inhibitors have a perticularly useful role in treating patients with diabetic nephropathy. They have also proved to be extremely useful in the treatment of heart failure, and after MI (myocardial infarction).
Primary Characteristics
It is of Synthetic origin and belongs to Benzapine.
Molecular Weight: 461 · pKa: 3.1, 5.3 · Solubility in Water: 1 in 13 · Solubility in Alcohol: > 1 in 2 · Non-proprietary name: Benazepril (HCl).

Pharmacokinetics
Absorption: Benazepril (HCl) has an oral bioavailability is 18.5% (±18.5%).
Distribution: Benazepril (HCl) has a volume of distribution is 8.7 liter. plasma protein binding is 92-95%.
Elimination: plasma half-life is 3 hr, renal excretion is > 1% (unchanged).
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Indications
Benazepril (HCl) is primarily indicated in conditions like Arterial hypertension, Congestive heart failure.
Contraindications
Benazepril (HCl) is contraindicated in conditions like Angioedema, Hypersensitivity.
Dosage
None recorded.
Drug Interactions
Always consult your physician for the change of dose regimen or an alternative drug of choice that may strictly be required.
Side Effects
Benazepril (HCl) produces potentially life-threatening effects which include Sustained tachycardia. Careful monitoring is needed with proper medical management.
Benazepril (HCl) is known to cause more or less tolerable side effects which are usually transient. These include Azotemia, Cough , Dizziness, Fatigue, Headache, Hypotension , Nausea, Somnolence , Vertigo.
Warnings / Precautions
Available Brands
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Multi-Ingredient Combinations
Storage Conditions
Drug Classification
- 1.12.3.3 — ACE inhibitors