L-Carnitine injections may not be appropriate for everyone. Additional medical evaluation or clearance may be necessary for individuals who:

• Are pregnant or breastfeeding
• Have a history of seizure disorders
• Have significant kidney disease or impaired kidney function
• Have a known allergy or sensitivity to L-carnitine or any ingredient in the formulation
• Have certain underlying medical conditions or take medications that may interact with treatment
• Are under 18 years of age

Eligibility is determined after reviewing your medical history, current medications, allergies, and treatment goals.

L-Carnitine is generally well tolerated, but possible side effects may include:

• Injection-site pain, redness, swelling, or irritation
• Nausea or stomach discomfort
• Diarrhea or abdominal cramping
• Headache
• A distinctive or "fishy" body odor
• Rare allergic reactions

The dose, frequency, and route of administration are determined by your healthcare provider based on your individual needs and the specific prescription.

At-Home Program: Patients approved for home administration receive prescribed medication and individualized instructions for safe use, storage, dosing, and injection technique.

L-Carnitine injections require medical evaluation and, when applicable, a prescription from a licensed healthcare provider. Treatment recommendations are individualized, and benefits are not guaranteed. Injectable formulations may be compounded depending on the product prescribed.

Compounded medications are not FDA-approved and have not undergone FDA review for safety, effectiveness, or manufacturing quality in the same manner as FDA-approved medications.

This information is for educational purposes and is not a substitute for individualized medical advice.

Lipotropic injections are not appropriate for everyone. Treatment eligibility is determined after an individualized medical evaluation. Treatment may not be appropriate, or may require additional evaluation, for patients who:

• Are pregnant, trying to become pregnant, or breastfeeding
• Have a known allergy or hypersensitivity to any ingredient in the prescribed formulation
• Have significant liver or kidney disease
• Have certain metabolic or medical conditions that may affect safe use
• Have a history of significant reactions to injectable vitamins or amino acids
• Have an active infection or significant skin inflammation at the intended injection site
• Take medications or supplements that may interact with ingredients in the prescribed formulation
• Have another medical condition that your provider determines makes treatment inappropriate

If your formulation contains lidocaine, additional screening for lidocaine or local-anesthetic allergy and relevant medical conditions may be necessary.

Potential side effects may include:

• Injection-site pain or tenderness
• Redness, swelling, bruising, or itching
• Nausea or gastrointestinal discomfort
• Headache
• Dizziness
• Temporary changes in energy or how you feel after injection
• Allergic or hypersensitivity reactions

Rarely, injectable products can cause more significant reactions. Contact your healthcare provider if you develop persistent or concerning symptoms. Seek immediate medical attention for symptoms of a severe allergic reaction, such as difficulty breathing, significant swelling, or other severe symptoms.

Metabolic and lipotropic injections are offered only after an individualized medical evaluation and when determined to be medically appropriate.

Formulations may vary by pharmacy, and the exact ingredients, concentrations, route of administration, dose, and frequency will be provided with your prescription.

When a compounded preparation is prescribed, patients should understand that compounded medications are not FDA-approved and do not undergo FDA premarket review for safety, effectiveness, or quality.

These injections should not be considered a substitute for appropriate nutrition, exercise, or FDA-approved weight-management treatment when medically indicated.

Weight loss, increased energy, improved metabolism, or other specific outcomes are not guaranteed. Individual results may vary.

Glutathione, B12, and zinc injections are not appropriate for everyone. Eligibility is determined after an individualized medical evaluation. Treatment may not be appropriate or may require additional evaluation for patients who:

• Are pregnant, trying to become pregnant, or breastfeeding
• Have a known allergy or hypersensitivity to an ingredient in the prescribed formulation
• Have significant kidney or liver disease
• Have certain blood, metabolic, or nutritional disorders requiring additional evaluation
• Have an active infection or significant inflammation at the intended injection site
• Have experienced a significant reaction to previous injectable vitamins, minerals, or antioxidants
• Take medications or supplements that could interact with the prescribed treatment
• Have another medical condition that your provider determines makes treatment inappropriate

Eligibility differs between glutathione, B12, and zinc. Having a precaution for one does not necessarily mean you cannot receive another.

Depending on the treatment and formulation, potential side effects may include:

• Injection-site pain or tenderness
• Redness, swelling, bruising, or itching
• Nausea or gastrointestinal discomfort
• Headache
• Dizziness
• Skin reactions
• Allergic or hypersensitivity reactions
• Other formulation-specific adverse effects

Zinc Precautions
Excessive or prolonged zinc supplementation may contribute to copper deficiency and other nutritional imbalances. Zinc treatment should therefore be individualized rather than used excessively without appropriate clinical oversight.

B12 Precautions
B12 injections may cause injection-site reactions and, rarely, hypersensitivity reactions. Individual response to supplementation varies.

Glutathione Precautions
Glutathione injections may cause local reactions and other adverse effects. Treatment should be prescribed according to the patient's medical history and individualized needs.

Antioxidant and nutritional injections are provided only after an individualized medical evaluation and when determined to be clinically appropriate.

The fact that B12, zinc, and glutathione occur naturally in the body or diet does not mean injectable formulations are appropriate or necessary for every patient.

When a compounded preparation is prescribed, patients should understand that compounded medications are not FDA-approved and do not undergo FDA premarket review for safety, effectiveness, or quality.

These treatments are not intended to diagnose, treat, cure, or prevent disease unless prescribed for an established medical indication.

Improved energy, immunity, appearance, performance, or general wellness is not guaranteed. Individual results may vary.

Tri-Immune is a compounded prescription medication and is not FDA-approved. Compounded medications are prepared by licensed compounding pharmacies for individual patients pursuant to a valid prescription when clinically appropriate. The FDA does not review compounded medications for safety, effectiveness, or quality before they are marketed.

Treatment requires a medical evaluation and prescription. Eligibility, dosing, route of administration, frequency, and duration are determined individually by the treating medical provider. Results vary, and no specific outcome is guaranteed.

This information is provided for general educational purposes and is not intended to diagnose, treat, cure, or prevent any disease. Tri-Immune should not be considered a substitute for recommended medical care, vaccination, or treatment of an infection or other medical condition.