Ascorbic Acid
Dosage & Administration Guidelines
| Species | Route | Dose | Frequency | Duration & Clinical Notes |
|---|---|---|---|---|
| Dog | PO | 10-50 mg/kg | q12h | Duration: Variable; often 2-4 weeks or as needed Notes: For copper hepatopathy, doses up to 100 mg/kg/day have been used. Monitor for oxalate urolithiasis. |
| Cat | PO | 10-30 mg/kg | q12h | Duration: Variable Notes: Use with caution in cats with a history of calcium oxalate uroliths. |
| Horse | PO | 10-20 g per horse (approximately 20-40 mg/kg) | q24h | Duration: Variable Notes: For EMND, higher doses (up to 50 mg/kg) may be used. Oral absorption is limited; IV administration may be more effective. |
| Cattle | SC or IM | 2-5 g per animal | q24h | Duration: 3-5 days Notes: Used as supportive therapy; not a substitute for specific treatment. |
| Small Ruminants | PO or SC | 1-3 g per animal | q24h | Duration: 3-5 days Notes: Limited data; use based on clinical judgment. |
| Rabbit | PO | 10-50 mg/kg | q24h | Duration: Variable Notes: Not routinely required; may be used as an antioxidant. |
| Bird/Poultry | PO (in water) | 100-500 mg/L of drinking water | q24h | Duration: 3-5 days Notes: Use fresh solution daily; ascorbic acid is unstable in water. |
| Guinea Pig | PO | 10-30 mg/kg | q24h | Duration: Continuous (dietary requirement) Notes: Deficiency leads to scurvy; ensure adequate dietary intake. |
Clinical Indications & Species Uses
- Treatment and prevention of vitamin C deficiency (scurvy) in species requiring dietary intake
- Antioxidant supplementation in various diseases
- Adjunct in the treatment of copper-associated hepatopathy (e.g., Bedlington Terriers)
- Supportive therapy for immune-mediated diseases
- Antioxidant support in cancer patients
- Wound healing support
- Urinary acidification (though efficacy is debated)
- Supportive therapy for feline infectious peritonitis (FIP) (limited evidence)
- Antioxidant support in chronic kidney disease
- Wound healing support
- Supportive therapy for exercise-induced oxidative stress
- Adjunct in the treatment of equine motor neuron disease (EMND)
- Wound healing support
- Supportive therapy for stress (e.g., transport, weaning)
- Adjunct in the treatment of mastitis (as an antioxidant)
- Supportive therapy for respiratory disease
- Supportive therapy for stress
- Antioxidant support in pregnancy toxemia
- Prevention and treatment of scurvy in species that require dietary vitamin C (e.g., some passerines)
- Antioxidant support during heat stress
- Guinea pigs: prevention and treatment of scurvy (essential dietary requirement)
- Primates: prevention and treatment of scurvy
- Fish: prevention of deficiency (e.g., in salmonids)
Pharmacology & Mechanism of Action
Drug Class: Vitamin | Pharmacological Group: Water-soluble vitamin (antioxidant)
Mechanism of Action: Ascorbic acid (vitamin C) is a water-soluble antioxidant that acts as a cofactor in numerous enzymatic reactions, including collagen synthesis (hydroxylation of proline and lysine), carnitine synthesis, neurotransmitter synthesis (dopamine to norepinephrine), and steroidogenesis. It also regenerates other antioxidants (e.g., vitamin E) and modulates immune function by enhancing neutrophil activity and lymphocyte proliferation. In veterinary medicine, it is used primarily for its antioxidant properties and to correct deficiency states.
Pharmacodynamics: Ascorbic acid scavenges reactive oxygen species (ROS) and reactive nitrogen species, protecting cells from oxidative damage. It enhances iron absorption by reducing ferric to ferrous iron. It is essential for the maintenance of connective tissue integrity, wound healing, and bone formation. In some species (e.g., primates, guinea pigs, and some fish), it is a vitamin because they lack L-gulonolactone oxidase, the enzyme required for its synthesis. In most domestic animals, it is synthesized in the liver, so deficiency is rare except under stress or certain diseases.
β‘ Pharmacokinetics Summary
Available Formulations & Strengths
Contraindications & Clinical Warnings
- Known hypersensitivity to ascorbic acid
- Patients with a history of calcium oxalate urolithiasis (high doses may increase oxalate excretion)
- Patients with glucose-6-phosphate dehydrogenase deficiency (rare in animals)
- Do not administer intravenously to patients with renal insufficiency (may cause hyperoxalemia)
- Use with caution in patients with renal disease, as high doses may increase oxalate load and risk of calcium oxalate crystal formation.
- High doses may interfere with urine glucose testing (false negatives) and fecal occult blood tests.
- In animals that synthesize vitamin C (e.g., dogs, cats), supplementation is generally unnecessary and may be harmful in excessive doses.
- Prolonged high-dose therapy may cause hemolysis in patients with glucose-6-phosphate dehydrogenase deficiency (rare in animals).
- Injectable solutions may cause tissue irritation if given IM or SC; administer slowly IV when possible.
- In food animals, observe withdrawal times; ascorbic acid is generally considered low risk, but regulatory guidelines should be followed.
Adverse Effects & Reactions
Common:
- Gastrointestinal upset (diarrhea, nausea) at high oral doses
- Tissue irritation at injection site
Serious / Severe:
- Calcium oxalate urolithiasis (with chronic high doses)
- Oxalate nephropathy (rare, with high IV doses)
- Hemolysis in G6PD-deficient patients
Rare:
- Allergic reactions
- Hyperoxalemia
- Interference with laboratory tests
Key Drug Interactions
| Interacting Drug / Class | Clinical Effect & Mechanism | Severity |
|---|---|---|
| Iron supplements | Ascorbic acid enhances iron absorption; may increase risk of iron toxicity if given concurrently. | Moderate |
| Corticosteroids | Corticosteroids may increase ascorbic acid requirements and decrease tissue levels. | Mild |
| Warfarin and other anticoagulants | High doses of ascorbic acid may antagonize the anticoagulant effect of warfarin. | Moderate |
| Fluphenazine and other phenothiazines | Ascorbic acid may decrease the therapeutic effect of phenothiazines. | Mild |
| Aluminum-containing antacids | Ascorbic acid may increase aluminum absorption, potentially increasing toxicity risk. | Mild |
Overdose & Toxicity Management
Signs of Toxicity:
- Gastrointestinal upset (diarrhea, abdominal pain)
- Polyuria and polydipsia (due to osmotic diuresis)
- Calcium oxalate crystalluria and urolithiasis
- Hemolysis (in G6PD-deficient patients)
Emergency Treatment Protocol: Discontinue ascorbic acid. Provide supportive care, including fluid therapy to promote diuresis and reduce oxalate concentration. Monitor renal function and urine sediment for crystals. In severe cases, consider alkalinization of urine to increase oxalate solubility. There is no specific antidote.
Food Animal Withdrawal Times
Ascorbic acid is generally considered a low-risk substance in food animals. However, for extra-label use, follow regulatory guidelines and consult the FARAD database for specific withdrawal times. In the US, ascorbic acid is not approved for use in food animals, but it is often used off-label; withdrawal times may be set by the veterinarian based on risk assessment.
Storage, Handling & Regulatory Information
Storage Temperature: Store at controlled room temperature (20-25Β°C, excursions permitted to 15-30Β°C). Protect from moisture.
Light Sensitivity: Light-sensitive β protect from direct exposure.
Handling & Special Conditions: Protect from light and moisture. Keep container tightly closed. Injectable solutions should be stored at room temperature and protected from light; do not freeze.
Dispensing Status: Over-The-Counter (OTC)
Approval Status: Ascorbic acid is generally recognized as safe (GRAS) for use in human foods and is available as a dietary supplement. In veterinary medicine, there are FDA-approved products for certain species (e.g., injectable for cattle), but many uses are extra-label.
Extra-Label (Off-Label) Use: Ascorbic acid is a non-prescription vitamin in most countries. In veterinary medicine, it is often used extra-label (e.g., in food animals) under the Animal Medicinal Drug Use Clarification Act (AMDUCA) in the US. Extra-label use requires a valid veterinarian-client-patient relationship and must follow label directions for approved drugs when available. For food animals, withdrawal times must be established by the veterinarian.
Clinical Pearls & Practice Notes
References & Literature
- π Plumb's Veterinary Drug Handbook
- π Papich Veterinary Pharmacology and Therapeutics
- π Compendium of Veterinary Products (CVP)