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Benazepril

Grade

Hypertension

Dosing Proposal

  • 0.25 – 0.5 mg/kg, PO, q12-24h (Müller and Mancinelli, 2022).


Major species extrapolation  (MSE) and anecdotal expert opinion in textbooks inform all dosing suggestions identified.

No Recommendations

There is no community consensus on diagnosing or staging rabbit hypertension. Therefore, until our understanding of rabbit hypertension is better developed, identifying ideal target patients, therapeutic strategies, and assessing hypertension treatment efficacy remains elusive.

Therapeutics

About Benazepril and Hypertension

Benazepril is a prodrug that inhibits the conversion of angiotensin-I to angiotensin-II by inhibiting angiotensin-converting enzyme (ACE) after being hydrolyzed in the liver to benazeprilat. 

Adverse Effects Profile

  • Severe CHF: Monitor for progressive azotaemia, especially where aggressive diuresis has recently occurred. Avoid use in cardiac output failure due, for example, to aortic stenosis.

  • GI Distress: Typically anorexia, vomiting, and diarrhoea.

  • Hypotension:  Animals may experience excessive hypotension, and fatigue, lethargy, ataxia, and incoordination may be observed. 

  • Azotaemia: Renal dysfunction, azotaemia and hyperkalemia may occur. Plasma creatinine concentration may increase at the start of therapy in patients with CKD or dehydration.

Contraindications

  • AKI: Avoid use in animals at risk of azotaemia as use may decrease GFR and worsen azotemia

  • Hypersensitivity: Avoid use in patients with known hypersensitivity to ACE inhibitors.

  • Hyponatremia or sodium depletion: Avoid use. 

  • Hypotension:  Avoid use in animals with or at risk of hypotension. 

  • Hypovolemia:  Avoid use. 

  • Coronary or cerebrovascular insufficiency:  Avoid use. 

  • Pre-existing hematologic abnormalities: Avoid use. 

  • SLE or Collagen Vascular Disease: Avoid use (e.g., systemic lupus erythematosus [SLE]). 

Reproductive Safety

  • Pregnancy: Avoid use. Benazepril crosses the placenta. Embryotoxic effects (foetal urinary tract malformation) were seen in trials with laboratory animals (rats) at maternally non-toxic doses (SPC data).

  • Lactation: Benazepril is not expected to cause adverse effects in an infant being nursed. However, in some countries, its use is contraindicated during pregnancy and lactation (SPC data).

  • Male Fertility: No data located.

  • Female Fertility: Avoid use. Benazepril reduced ovary/oviduct weights in cats when administered daily at 10 mg/kg body weight for 52 weeks (SPC data).

  • Neonates: Benazepril is not expected to cause adverse effects in an infant being nursed (SPC data).

Interactions

  • Anti-hypertensive Agents: e.g. calcium channel blockers, β-blockers or diuretics), anaesthetics or sedatives may lead to additive hypotensive effects (SPC data).

  • NSAIDs: e.g., carprofen, meloxicam, robenacoxib): can lead to reduced anti-hypertensive efficacy or impaired renal function (SPC data).

Alternative Products 

  • We refer clinicians to current ACVIM Hypertension recommendations. 

Alternative Protocols

  • We refer clinicians to current ACVIM Hypertension recommendations. 

Formulations

  • Oral Forms:  2.5 mg, 5mg and 20mg Tablets

  • UK Availability: Sole agent or combined with other diuretics such as hydrochlorothiazide.

Evidence


  • Li, J., Wanchun, C., 1997. Benazepril on tissue angiotensin-converting enzyme and cellular proliferation in restenosis after experimental angioplasty. J Cardiovasc Pharmacol 30, 790–797. https://doi.org/10.1097/00005344-199712000-00014

  • Müller, K., Mancinelli, E., 2022. Cardiology in Rabbits and Rodents–Common Cardiac Diseases, Therapeutic Options, and Limitations. Veterinary Clinics of North America: Exotic Animal Practice, Cardiology 25, 525–540. https://doi.org/10.1016/j.cvex.2022.01.006

  • Pariaut, R., 2009. Cardiovascular Physiology and Diseases of the Rabbit. Veterinary Clinics of North America: Exotic Animal Practice, Cardiology 12, 135–144. https://doi.org/10.1016/j.cvex.2008.08.004

  • Reusch, B., 2005. Investigation and management of cardiovascular disease in rabbits. In Practice 27, 418–425. https://doi.org/10.1136/inpract.27.8.418

  • Yamamoto, S., Takemori, E., Hasegawa, Y., Kuroda, K., Nakao, K., Inukai, T., Sakonjyo, H., Nishimura, T., Nishimori, T., 1991. General pharmacology of the novel angiotensin converting enzyme inhibitor benazepril hydrochloride. Effects on cardiovascular, visceral and renal functions and on hemodynamics. Arzneimittelforschung 41, 913–923.

 

Expert Opinion


  • 1317822 : Extrapolation of pharmacological properties in man and veterinary species. Some material employed in collating the data displayed here was taken from veterinary product datasheets or extrapolated from pharmacology texts.


Datasheets Accessed


Monograph Details

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