Bethanechol for Animals

Bethanechol

Bethanechol stimulates detrusor and gastrointestinal smooth muscle. Veterinary efficacy evidence is limited.

Group

Muscarinic agonist

Mechanism of Action

Directly activates muscarinic receptors and resists acetylcholinesterase hydrolysis.

Dose Rates

Dogs

Use / stageDoseRouteScheduleInstructions
Urinary bladder atony5–15 mg/animalPOEvery 8 hEmpirical size-related doses: small dogs 2.5 mg, medium dogs 5 mg, large dogs 15 mg. The general range is not a validated weight-band table.
Urinary bladder atony2.5 mg/animalPOEvery 8 hSmall-dog alternative.
Urinary bladder atony5–25 mg/animalPOEvery 8–12 h
Urinary bladder atony2.5–25 mg/animalPOEvery 8 h
Reduced esophageal sphincter tone0.5–1 mg/kgPOEvery 8 h
Dysautonomia1.25–5 mg/animalPOEvery 24 h
Divided-dose dysautonomia treatmentReference onlyPO2.5–7.5 mg total orally divided every 8–12 hours; the passage does not unambiguously distinguish the daily total from the amount per administration.
Dysautonomia0.05 mg/kgSCEvery 12 hIncrease slowly according to response; have atropine available for cholinergic toxicity.
Dysautonomia1.25–5 mg/animalPOEvery 12 h

Cats

Use / stageDoseRouteScheduleInstructions
Urinary bladder atony1.25–5 mg/animalPOEvery 8 h
Urinary bladder atony1.25–7.5 mg/animalPOEvery 8–12 h
Urinary bladder atony1.25–7.5 mg/animalPOEvery 8 h
Dysautonomia1.25–5 mg/animalPOEvery 24 h
Divided-dose dysautonomia treatmentReference onlyPO2.5–7.5 mg total orally divided every 8–12 hours; the passage does not unambiguously distinguish the daily total from the amount per administration.

Horses

Use / stageDoseRouteScheduleInstructions
Gastrointestinal motility stimulation0.025 mg/kgSCOnceHistorical regimen; efficacy for gastrointestinal stasis is questionable.
Urinary bladder atony0.025–0.075 mg/kgSCEvery 8 h
Urinary bladder atony0.25–0.75 mg/kgPOEvery 6–12 hOnly if weak detrusor contractions remain; dose differs substantially from SC administration.
Postoperative bladder atony0.4 mg/kgPOEvery 8–12 hFoals only; withdraw gradually as bladder function returns.

Cattle

Use / stageDoseRouteScheduleInstructions
Gastrointestinal motility stimulation0.07 mg/kgSCOnceHistorical regimen; efficacy for gastrointestinal stasis is questionable.
Cecal dilation without torsion0.07 mg/kgSCEvery 8 hUp to 2 days; Only for stable or mildly affected cattle still passing feces, without rectal evidence of torsion or retroflexion. Combine fluids and other indicated care; no improvement in 24 hours requires reassessment for surgery.

Indications

  • Urinary bladder atony
  • Historical gastrointestinal motility stimulation

Contraindications

  • Suspected urinary or gastrointestinal obstruction.
  • Compromised bladder integrity, recent gastrointestinal anastomosis, peritonitis, peptic ulceration or inflammatory gastrointestinal lesions.
  • Severe bradycardia, hypotension, asthma, epilepsy or hyperthyroidism.
  • Hypersensitivity to bethanechol.

Interactions

  • Atropine and other anticholinergics oppose its effects.
  • Other cholinergic drugs can produce additive cholinergic toxicity.
  • Quinidine and procainamide may oppose the response; ganglionic blockers can increase gastrointestinal and hypotensive effects.

Adverse effects

  • Abdominal cramping and diarrhea
  • Circulatory depression

Toxicity

Cholinergic excess causes salivation, diarrhea, bradycardia, bronchospasm and potentially circulatory collapse. Atropine antagonizes muscarinic toxicity; maintain airway and cardiovascular support.

Preparations

PreparationFormStrengthRoute
Bethanechol 5 mg tabletTablet5 mg / tabletPO
Bethanechol 10 mg tabletTablet10 mg / tabletPO
Bethanechol 25 mg tabletTablet25 mg / tabletPO
Bethanechol 50 mg tabletTablet50 mg / tabletPO
Bethanechol 5 mg/mL injectionInjection5 mg / mLSC
Compounded bethanechol chloride 5 mg/mL oral suspension
Specific Ora-Plus/Ora-Sweet formulation; 60-day reported potency at 5°C or 25°C protected from light.
Oral Liquid5 mg / mLPO

Monitoring and Administration

Exclude obstruction before treatment. Monitor urination, gastrointestinal function and cardiovascular response.

Only subcutaneous injection is described. Oral treatment is generally preferred in small animals. Large-animal use for gastrointestinal stasis has uncertain efficacy and is not recommended routinely.

Follow voided volume, bladder size, urination frequency and gastrointestinal tolerance. Exclude mechanical obstruction; increased urethral tone may require a separate outflow-relaxing drug. Give oral doses on an empty stomach unless this is poorly tolerated.

Compounding stability is vehicle-specific: twelve 50 mg tablets in 60 mL Ora-Plus, made to 120 mL with Ora-Sweet or Ora-Sweet SF, gives 5 mg/mL and has reported 60-day potency at 5°C or 25°C protected from light. Do not generalize this to other aqueous vehicles.

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