Start or Transfer a Prescription
Send Trinova Health your prescription details, or ask us to coordinate a transfer from another pharmacy.
Trinova Health prepares patient-specific low-dose naltrexone in the strength and dosage form authorized by a licensed prescriber. Our pharmacy team can answer formulation questions and help coordinate a new prescription or transfer.
Choose the path that best matches your situation.
Send Trinova Health your prescription details, or ask us to coordinate a transfer from another pharmacy.
Call to discuss prescription intake, formulation questions, shipping, or account setup.
Trinova Health compounds medication only after receiving a patient-specific prescription from a licensed practitioner.
Choose the method that works best for your practice.
Search for Trinova Health in Tampa, Florida, within your e-prescribing system.
Fax the patient-specific prescription to 888-288-8253.
Call 844-219-2139 or email contact@trinovahealth.com.
This educational information does not replace the instructions or clinical judgment of the prescribing practitioner or dispensing pharmacist.
Naltrexone is an opioid receptor antagonist. FDA-approved oral naltrexone products use a standard dose for alcohol dependence and blockade of the effects of externally administered opioids. “Low-dose naltrexone” describes substantially smaller doses that clinicians may prescribe off-label for selected patients.
Low-dose naltrexone is not FDA-approved for chronic pain, fibromyalgia, autoimmune disease, or other commonly discussed off-label uses. Published studies have produced mixed results, and the strength of evidence varies by condition. Treatment decisions should be individualized by the prescriber.
A compounded LDN prescription may be useful when the prescribed strength or dosage form is not commercially available. The active ingredient, capsule or tablet composition, and inactive ingredients are selected according to the prescription and pharmacy review.
Naltrexone blocks opioid receptors and may reduce the effect of opioid pain medicines, cough medicines, or antidiarrheal products. Starting naltrexone too soon after opioid use may trigger abrupt withdrawal.
Signs of a severe allergic reaction, severe or persistent abdominal pain, symptoms of acute hepatitis such as yellowing of the skin or eyes, severe depression or suicidal thoughts, or symptoms of precipitated opioid withdrawal.
Reported effects with naltrexone may include nausea, stomach discomfort, headache, dizziness, fatigue, nervousness, sleep changes, or vivid dreams. The likelihood and severity can differ by patient and dose.
Contact the prescriber or pharmacist about any persistent, worsening, or unexpected reaction. This page does not list every possible adverse effect or interaction.
Naltrexone hydrochloride, in the patient-specific strength stated on the prescription label.
Inactive ingredients vary by formulation and may include capsule shells, fillers, binders, flavoring agents, or suspending vehicles. Tell Trinova Health about allergies or sensitivities before the prescription is prepared.
Follow the storage directions printed on the prescription label. Protect the medication from conditions listed on the label, keep it out of reach of children and pets, and review Trinova Health’s shipping policies for current delivery information.
Our pharmacy team is available to help patients and practitioners with prescription intake and formulation questions.