Benazepril
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.
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.
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
Item Type Attachment URL https://www.vmd.defra.gov.uk/productinformationdatabase/files/SPC_Documents/SPC_130807.PDF Accessed 01/10/2023, 06:09:35 Date Added 01/10/2023, 06:09:35 Modified 01/10/2023, 06:14:04 Fortekor 2.5 mg Tablets for Cats and Dogs.pdf
Item Type Attachment URL https://www.vmd.defra.gov.uk/productinformationdatabase/files/SPC_Documents/SPC_862595.PDF Accessed 01/10/2023, 06:12:38 Date Added 01/10/2023, 06:12:38 Modified 01/10/2023, 06:15:03 MiPet Benazapet 2.5 mg Tablets for cats and dogs