.png)
Longetivity medication, personalized to you
Longetivity
medication, personalized to you
This is more than just the beginning — it’s where your personalized care journey truly takes shape, tailored to your unique needs and goals.
Care, simplified
Answer some questions about your health history, lifestyle, and goals.
A medical professional will review your intake and determine what’s right for you.
If prescribed, you’ll get a customized holistic plan designed to work for you.
Get unlimited online access to follow-ups, adjustments, and answers to questions.
Compounded Semaglutide
*Compounded medications may be prescribed by physicians but have not been FDA regulated for safety, effectiveness, or quality. FDA-approved medicines containing semaglutide are available.
WARNING
Please contact your doctor ASAP and seek in-person care immediately if a side effect becomes problematic or you experience:
- Severe nausea and/or vomiting resulting in dehydration—it is important to stay well hydrated and drink plenty of fluids while on this medication
Kidney problems/kidney failure - vomiting, nausea, diarrhea can cause dehydration and kidney issues and make kidney problems worse in individuals who have pre-existing kidney conditions; may sometimes lead to the need for hemodialysis - Thyroid C-Cell Tumor: Trouble swallowing, hoarseness, a lump or swelling in your neck, or shortness of breath (see black box warning below)
- Pancreatitis: Severe pain in your abdomen or back that will not go away
- Acute gallbladder disease - Pain in the middle or right upper stomach, fever, white parts of your eyes turn yellow or skin turns yellow, nausea/vomiting. If gallstones or inflammation of the gallbladder is suspected further studies are needed.
- Hepatitis/Elevated liver enzymes/Jaundice
- Diabetic retinopathy problems: Changes in vision in those with type II diabetes, particularly vision problems may worsen in those with a history of diabetic retinopathy
- Severe gastrointestinal disease - may cause gastrointestinal disease; do not use if you have a history of severe gastrointestinal disease
- Signs of low blood sugar (for example, dizziness, weakness, shakiness, jitteriness, headache, anxiety/mood changes, rapid heartbeat, confusion, slurred speech, sweating, or lightheadedness). While this is rare with GLP-1s, if it occurs, please seek in-person care immediately. If you have these symptoms, try having liquid or food containing sugar (around 15-20 grams) —drinking juice, having regular soda, or eating some hard candies right away, as this will help raise your blood sugar quickly. If taken with insulin or an insulin secretagogue (i.e. sulfonylurea such as Glipizide, glimepiride, and glyburide) it is best to talk to your healthcare provider about possibly lowering the dose of these medications to lower the risk of hypoglycemia.
- Increasing heart rate
- Worsening depression, behavior changes, or suicidality
Never share the semaglutide with other people
Drug Interactions
As with other medications, compounded semaglutide can interact with alcohol and certain prescription and non-prescription medications and herbal products. The risk of hypoglycemia is increased when combined with insulin or insulin secretagogues such as sulfonylureas. Compounded semaglutide delays gastric emptying and may impact the absorption of oral medications. If you are on papillary hormone medication, prior to starting compounded semaglutide, please review the timing of taking your papillary hormone medication with the doctor who prescribes it as it may need to be adjusted. The drug levels of medications with narrow therapeutic windows (ie warfarin) should be monitored closely while on compounded semaglutide.
Please consult the pharmaceutical packaging for a full list of side effects, warnings, interactions and additional information.
To report suspected adverse reactions to compounded semaglutide, contact the FDA at 1-800-FDA-1088 or www.fda.gov/medwatch.
In case of emergencies, please call 911 or go to the nearest emergency room.
Note: The above statements have not been evaluated by the Food and Drug Administration. This product is not intended to diagnose, treat, cure, or prevent any disease.
BLACK BOX WARNING
GLP-1s are contraindicated in individuals with a history of medullary thyroid carcinoma, a family history of such, or in patients with multiple endocrine neoplasia syndrome type 2. Do not take them if you have ever had thyroid cancer. In studies with rodents, GLP-1s caused thyroid tumors, including thyroid cancer; it is not known if they will cause thyroid tumors or cancer in humans. Please notify your doctor ASAP if you develop trouble swallowing, hoarseness, a lump or swelling in your neck, or shortness of breath.
If you experience a medical emergency, call 911 or go to the nearest emergency room.
Tell your healthcare provider about your medical history prior to taking semaglutide.
Avoid alcohol while taking this medication. If you’re taking diabetes medications, please discuss this with your prescribing doctor before starting semaglutide, as your diabetes medications may need to be adjusted as you lose weight.
Use adequate contraception while taking this medication. Do not take this medication if pregnant, trying to get pregnant or breastfeeding. If you plan to become pregnant, this medication needs to be stopped at least 2 months before trying. This medication may cause fetal harm.
Notify your doctor if you have kidney, liver, or pancreas problems.
Stop using semaglutide and call your healthcare provider immediately if you have severe stomach or abdomen pain that will not go away, with or without vomiting.
Stop using semaglutide and get medical help right away if you have any symptoms of a serious allergic reaction, including swelling of your face, lips, tongue, or throat; problems breathing or swallowing; severe rash or itching; fainting or feeling dizzy; or very rapid heartbeat.
Serious hypersensitivity reactions (e.g., anaphylaxis and angioedema) have been reported. Discontinue semaglutide if suspected and promptly seek medical advice.
NAD+ Injection: Important Safety Information
1. Introduction
Nicotinamide Adenine Dinucleotide (NAD+) is a coenzyme found in all living cells, involved in critical metabolic processes. NAD+ injections are sometimes used for various wellness purposes. Please note that NAD+ injections may not be evaluated or approved by the U.S. Food and Drug Administration (FDA) for safety, effectiveness, or quality. If you have any questions about NAD+ therapy, consult a qualified healthcare professional.
2. Purpose & Benefits
- NAD+ may be administered for potential support of energy metabolism, cellular repair, or other wellness goals.
- This information does not constitute medical advice regarding indications or dosage and is provided for educational purposes only.
3. Contraindications
You should not receive NAD+ injections if you:
- Have a known allergy or hypersensitivity to NAD+ or any of the injection components.
- Are pregnant, planning to become pregnant, or breastfeeding, unless specifically advised by your healthcare provider.
- Have severe or unstable medical conditions (e.g., uncontrolled diabetes, end-stage renal disease, significant heart or liver disease) without first consulting a physician.
4. Potential Risks & Side Effects
While many individuals tolerate NAD+ injections well, side effects can occur. Contact your healthcare provider immediately if any symptoms worsen or become unmanageable. Potential side effects include:
- Injection Site Reactions
- Redness, swelling, or pain at the injection site.
- Bruising or minor bleeding.
-
- Gastrointestinal Disturbances
- Nausea, vomiting, or diarrhea.
- Abdominal discomfort or cramping.
-
- Headache or Dizziness
- May occur shortly after injection.
- If severe or persistent, seek medical attention.
-
- Changes in Energy Levels
- Some individuals report fatigue or jitteriness, especially if combined with other stimulants.
-
- Allergic Reactions
- Rash, itching, swelling (including of the face, lips, tongue, or throat), or difficulty breathing.
- Seek emergency care if you suspect a serious allergic reaction (anaphylaxis).
5. Warnings & Precautions
- Not FDA-Approved
-
- NAD+ injections have not been evaluated by the FDA for safety or efficacy.
- If you prefer FDA-approved treatments, discuss alternatives with your healthcare provider.
-
- Medical Supervision Required
- NAD+ injections should be administered by a qualified healthcare professional or under professional guidance, following all recommended safety protocols.
-
- Pre-Existing Conditions
- Inform your healthcare provider of any heart, kidney, liver, or other medical conditions.
- Discuss any concerns regarding potential interactions with existing medications or supplements.
-
- Use in Specific Populations
- Safety and effectiveness in children have not been established.
- Pregnant or nursing women should consult a physician before use.
-
- Monitor for Unusual Symptoms
- Report any unexpected changes in mood, behavior, or physical health (e.g., extreme fatigue, chest pain, shortness of breath).
6. Drug Interactions
- NAD+ may interact with certain prescription or over-the-counter medications, herbal supplements, or dietary regimens.
- Tell your healthcare provider about all medications and supplements you take before starting NAD+ injections.
- Watch for potential changes in how other medications work, as NAD+ could theoretically affect metabolic pathways.
7. Administration & Dosage
- Administration Method
- Typically administered intramuscularly (IM) or Subcutaneous (SUBQ) under medical supervision.
- Proper aseptic technique is critical to minimize risks of infection or injection site complications.
- Dosage
- The appropriate dose varies based on individual factors (age, weight, underlying health conditions).
- Follow the dosage and schedule as prescribed by your healthcare provider.
- Do not self-adjust or discontinue injections without consulting your provider.
8. Reporting Adverse Events
- If you experience concerning side effects or a serious adverse event, seek immediate medical care.
- You can also report suspected adverse reactions to the FDA’s MedWatch Program at 1-800-FDA-1088 or at www.fda.gov/medwatch.
9. Additional Precautions & Tips
- Hydration: Staying well-hydrated may help mitigate some side effects like headaches or dizziness.
- Lifestyle Factors: Aim for a balanced diet, regular exercise, and healthy sleep to optimize any potential benefits of NAD+ therapy.
- Follow-Up: Schedule follow-up appointments or lab tests if your healthcare provider deems them necessary to monitor any changes while on NAD+ therapy.
10. Disclaimer
- These statements have not been evaluated by the Food and Drug Administration.
- NAD+ injections are not intended to diagnose, treat, cure, or prevent any disease.
- This document is for informational purposes only and is not a substitute for professional medical advice, diagnosis, or treatment.
For questions or concerns about NAD+ injections, potential benefits, or side effects, please consult a qualified healthcare provider.
Sermorelin: Important Safety Information
1. Introduction
- What is Sermorelin?
Sermorelin is a synthetic peptide analog of growth hormone–releasing hormone (GHRH). It works by stimulating the pituitary gland to produce and secrete natural growth hormone (GH). - Regulatory Status
Sermorelin may be prescribed or compounded by certain healthcare providers but may not be approved by the U.S. Food and Drug Administration (FDA) for all uses. If you prefer only FDA-approved medications for your condition, please consult your healthcare provider for alternatives.
2. Potential Benefits & Indications
- Common Uses
Some practitioners use sermorelin to help address growth hormone deficiencies, promote lean body mass, support energy levels, or assist with certain aspects of aging. - Limitations
The efficacy of sermorelin for anti-aging or athletic performance enhancement is not conclusively established in large-scale clinical trials. This product is not intended to diagnose, treat, cure, or prevent any disease beyond those conditions specifically recognized by your healthcare professional.
3. Contraindications
You should not use sermorelin if you:
- Have an active malignancy, especially related to the pituitary gland or hypothalamus.
- Have a known hypersensitivity or allergy to sermorelin or any of its components.
- Are pregnant, planning to become pregnant, or breastfeeding, unless advised otherwise by a qualified healthcare professional.
- Have severe or unstable medical conditions (e.g., uncontrolled diabetes, advanced kidney or liver disease) without close medical supervision.
4. Warnings & Precautions
-
- Not FDA-Approved for All Uses
- Sermorelin may be used off-label for certain conditions. Its safety and efficacy for those uses are not fully evaluated by the FDA.
-
- Consult a Healthcare Professional
- Provide your full medical history to your healthcare provider before starting sermorelin.
- Discuss any other medications, supplements, or therapies you are using, as these can impact sermorelin’s efficacy or risk profile.
-
- Pre-Existing Conditions
- If you have diabetes, thyroid disorders, or any endocrine-related condition, careful monitoring may be needed because sermorelin can affect hormone balance.
-
- Use in Specific Populations
- The safety of sermorelin in children, pregnant women, or nursing mothers has not been thoroughly established outside of specific medical indications.
- Use only under professional guidance if you belong to these populations.
5. Potential Side Effects
Contact your healthcare provider if any symptoms become severe or do not resolve:
- Injection Site Reactions
- Redness, pain, swelling, or itching at the site of injection.
- If signs of infection (e.g., warmth, pus, significant tenderness) occur, seek medical attention.
-
- Flushing or Headaches
- Some people may experience flushing, mild headaches, or lightheadedness.
- If headaches are persistent or severe, discontinue use and consult your healthcare provider.
-
- Nausea or Dizziness
- Occasional nausea or dizziness can occur.
- Discontinue and speak with a healthcare provider if these symptoms worsen or persist.
-
- Increased Hunger
- A change in appetite or mild GI discomfort may be noticed.
-
- Allergic Reactions
- Rash, hives, swelling of the face, lips, tongue, or throat, or difficulty breathing may signal a serious allergic reaction.
- Seek immediate medical care if anaphylaxis is suspected.
6. Drug Interactions
- Other Medications/Supplements
- Sermorelin may interact with medications that influence the endocrine system, glucose metabolism, or other peptides/hormones.
- Always inform your healthcare provider about all prescription, over-the-counter medications, and supplements you use.
7. Administration & Dosage
-
- Administration Method
- Typically administered as a subcutaneous (under the skin) injection.
- Injections should be performed as directed by a qualified healthcare professional or according to detailed instructions provided.
-
- Dosage
- Dosage and frequency vary based on individual factors such as age, body weight, and treatment goals.
- Do not exceed prescribed dosage without consulting your healthcare provider.
-
- Timing & Technique
- Your healthcare provider may advise specific timing (e.g., bedtime) to optimize the natural growth hormone cycle.
- Proper injection technique is essential to minimize side effects and ensure effectiveness.
8. Monitoring & Follow-up
- Lab Tests
- Your healthcare provider may recommend periodic blood tests (e.g., IGF-1 levels) to monitor hormone levels and treatment response.
- Physical Check-ups
- Regular check-ups may be necessary to track weight, body composition, or other health indicators.
9. Storage & Handling
- Storage
- Store sermorelin according to the temperature guidelines provided on the label or by your pharmacist (often refrigerated).
- Shelf Life
- Do not use beyond the expiration date. Discard if the product changes color or appears contaminated.
- Safety
- Keep all medications out of the reach of children.
- Never reuse needles or syringes; follow proper disposal instructions.
10. Adverse Event Reporting
- Severe Reactions
- Discontinue use and seek immediate medical attention if you experience severe or unusual side effects.
- FDA Reporting
- You or your healthcare provider can report suspected adverse reactions to the FDA’s MedWatch Program at 1-800-FDA-1088 or via www.fda.gov/medwatch.
11. Disclaimer
- Not Evaluated by the FDA
- These statements have not been evaluated by the Food and Drug Administration, and sermorelin is not FDA-approved to diagnose, treat, cure, or prevent any condition outside of recognized uses.
- Consult a Professional
- This information is for educational purposes only and should not replace professional medical advice, diagnosis, or treatment.
- Individual Variation
- Responses to sermorelin may vary. Always follow the advice of a qualified healthcare provider regarding initiation, continuation, or modification of therapy.
Questions or Concerns?
If you have any questions regarding sermorelin injections, dosage, benefits, or potential side effects, please consult your qualified healthcare provider.
Glutathione Injection: Important Safety Information
1. Introduction
- What is Glutathione?
Glutathione is a tripeptide (made from glutamate, cysteine, and glycine) naturally present in cells, where it plays a key role in antioxidant defense and various metabolic processes. - Regulatory Status
Glutathione injections are not evaluated or approved by the U.S. Food and Drug Administration (FDA) for specific medical indications, dosage, safety, or effectiveness. If you prefer only FDA-approved medications, please discuss alternatives with your healthcare provider.
2. Potential Benefits & Limitations
- Common Uses
Some practitioners may use glutathione injections for antioxidant support, skin health, or general wellness. - Limitations
The benefits are based on limited studies and anecdotal reports. Glutathione injections are not intended to diagnose, treat, cure, or prevent any disease.
3. Contraindications
You should not receive glutathione injections if you:
- Have a known allergy or hypersensitivity to glutathione or any component in the formulation.
- Are pregnant, planning to become pregnant, or breastfeeding without discussing the potential risks and benefits with a qualified healthcare professional.
- Have serious or unstable medical conditions (e.g., end-stage kidney disease, severe liver disease, or uncontrolled diabetes) without close medical supervision.
4. Warnings & Precautions
- Not FDA-Approved
- Glutathione injection is not FDA-approved, and its safety or efficacy profile for specific indications is not established.
-
- Consult a Healthcare Professional
- Before starting glutathione injections, discuss your entire medical history, current medications, and supplements with your healthcare provider.
- Talk about potential benefits, risks, and whether you need any follow-up lab tests or monitoring.
-
- Use in Specific Populations
- The safety in children, pregnant women, breastfeeding mothers, or immunocompromised patients is unknown.
- Use only under medical guidance if the potential benefits outweigh the risks.
-
- Allergies or Sensitivities
- Disclose any history of allergies or adverse reactions to medications, especially those administered via injection.
5. Potential Side Effects
While many individuals tolerate glutathione injections without major issues, some side effects may occur. Contact your healthcare provider if any symptoms persist or worsen.
- Injection Site Reactions
- Redness, swelling, pain, or bruising at the injection site.
- If you notice persistent or severe discomfort, discoloration, or infection-like symptoms (e.g., warmth, pus), consult your healthcare provider promptly.
-
- Allergic Reactions
- Itching, rash, hives, shortness of breath, or swelling of the face, lips, tongue, or throat.
- Seek immediate medical attention if you suspect a serious allergic reaction (anaphylaxis).
-
- Nausea or Gastrointestinal Distress
- Mild nausea, stomach upset, or diarrhea can occur.
- Report severe or persistent GI symptoms to your provider.
-
- Headache or Lightheadedness
- Might occur after injection; if severe, contact your healthcare provider.
-
- Other Possible Effects
- Changes in skin pigmentation, dizziness, fatigue, or other unanticipated symptoms.
- Discontinue and consult a professional if unusual or concerning effects arise.
6. Drug Interactions
- Medication and Supplement Considerations
- Glutathione may theoretically interact with certain prescription or over-the-counter medications, vitamins, or herbal products, especially those affecting oxidation-reduction or detoxification pathways.
- Always inform your healthcare provider of all medications and supplements you take to avoid potential interactions or complications.
7. Administration & Dosage
- Administration Method
- Glutathione injections are typically given subcutaneously (SUB-Q) or intramuscularly (IM).
- Administration should be performed by a qualified healthcare professional or under appropriate medical supervision.
-
- Dosage
- There is no universally accepted standard dosing protocol for glutathione injection.
- Your healthcare provider will determine the dosage and frequency based on your individual health status and treatment goals.
-
- Monitoring
- Depending on the reason for use, your provider may recommend regular lab tests (e.g., liver function, kidney function) to monitor safety and effectiveness.
8. Storage & Handling
- Temperature
- Store the product as indicated on the label or as instructed by your pharmacist (often in a refrigerator, protected from direct sunlight).
- Sterility
- Ensure vials or ampules are used in a sterile manner. Never reuse syringes or needles.
- Expiration
- Do not use beyond the expiration date. Inspect the product for discoloration or particulate matter before each use; discard if present.
9. Adverse Event Reporting
- If you experience a severe or unexpected reaction, discontinue use and seek immediate medical attention.
- You or your healthcare provider can report suspected adverse reactions to the FDA’s MedWatch Program at 1-800-FDA-1088 or online at www.fda.gov/medwatch.
10. Disclaimer
- Not Evaluated by the FDA: These statements have not been evaluated by the Food and Drug Administration, and glutathione injections are not FDA-approved to diagnose, treat, cure, or prevent any disease.
- Consult a Professional: This information is for educational purposes only and does not replace professional medical advice.
- No Guarantee: Individual responses and results may vary.
Questions or Concerns?
For any additional information regarding glutathione injections, including potential benefits, side effects, or dosage considerations, please consult your qualified healthcare provider.
Lipotropic (MIC) & B12 Injection: Important Safety Information
1. Introduction
- What Are Lipotropic (MIC) Injections?
Lipotropic injections often contain a combination of Methionine, Inositol, and Choline (MIC). These components may support liver function, metabolism, and fat processing when used alongside a proper diet and exercise regimen. - B12 Supplementation
Vitamin B12 (commonly cyanocobalamin or methylcobalamin) is frequently added to lipotropic injections to support energy metabolism and red blood cell formation. - Regulatory Status
Certain formulations of MIC and B12 injections may not be evaluated or approved by the U.S. Food and Drug Administration (FDA) for weight loss or other off-label uses. If you prefer only FDA-approved treatments, please consult your healthcare provider about alternatives.
2. Potential Uses & Benefits
- Weight-Management Support
MIC injections are sometimes used as an adjunct to lifestyle interventions (diet and exercise) for individuals seeking to support healthy metabolism. - Nutritional Support
B12 supplementation may help address or prevent deficiency, supporting energy levels and proper red blood cell production. - Limitations
This product is not intended to diagnose, treat, cure, or prevent any disease and is typically part of a broader health or weight-management plan. Efficacy for weight loss varies among individuals and has limited clinical trial data.
3. Contraindications
You should not receive MIC+B12 injections if you:
- Have a known allergy or hypersensitivity to any of the ingredients (e.g., methionine, inositol, choline, vitamin B12) or their preservatives.
- Are pregnant, trying to conceive, or breastfeeding, unless your healthcare provider has deemed it safe.
- Have severe or unstable medical conditions (e.g., advanced liver or kidney disease) without consulting a qualified healthcare professional.
4. Warnings & Precautions
- Not FDA-Approved for Weight Loss
- While sometimes used in weight-management protocols, lipotropic injections have not been formally evaluated or approved by the FDA for weight loss.
-
- Consult Your Healthcare Provider
- Discuss your full medical history, including any chronic conditions, allergies, or autoimmune disorders.
- Inform your provider about all medications, supplements, and herbs you currently take, as these can interact with MIC or B12.
-
- Pre-Existing Conditions
- Use caution if you have a history of cardiovascular disease, diabetes, or hormone-related conditions.
- Lab monitoring (e.g., liver function, B12 levels) may be recommended depending on your clinical situation.
-
- Pediatric or Geriatric Use
- Safety and efficacy in children or the elderly have not been fully established for weight-management or off-label indications.
- Use only under professional guidance in these populations.
5. Potential Side Effects
While many individuals tolerate MIC+B12 injections well, side effects can occur. Contact your healthcare provider if any of the following become severe or persist:
- Injection Site Reactions
- Redness, swelling, tenderness, or bruising at the injection site.
- If signs of infection (e.g., pus, warmth, significant redness) develop, seek medical attention.
-
- Gastrointestinal Discomfort
- Nausea, upset stomach, or mild diarrhea.
- Severe or persistent GI symptoms should be evaluated by a healthcare professional.
-
- Allergic Reactions
- Rash, itching, hives, swelling of the face or throat, difficulty breathing (possible anaphylaxis).
- Discontinue use and seek immediate medical help if you suspect a serious allergic reaction.
-
- Headache, Dizziness, or Fatigue
- Some individuals may experience mild headaches, dizziness, or fatigue following the injection.
- Stop use and consult your provider if these symptoms are severe or prolonged.
-
- Unusual Urine Odor
- Methionine can sometimes cause a distinct odor in urine; generally not harmful but discuss with your provider if concerning.
6. Drug Interactions
- Other Medications and Supplements
- Lipotropic agents and high-dose B12 may interact with certain prescription drugs (e.g., levodopa, methotrexate) or other supplements.
- Always inform your healthcare provider of all medications, supplements, or herbal products you take.
7. Administration & Dosage
- Administration Method
- Injections are typically administered intramuscularly (IM) or subcutaneously (SQ).
- A qualified healthcare professional or a person trained in proper injection technique should administer.
-
- Dosage & Frequency
- Dosage and frequency can vary widely, depending on individual health status and goals.
- Follow your provider’s specific instructions and do not exceed the recommended dose without medical guidance.
-
- Monitoring
- Your provider may recommend periodic blood work (e.g., vitamin B12 levels, liver function tests) to assess effectiveness and detect potential issues.
8. Storage & Handling
- Proper Storage
- Refrigeration may be required for certain lipotropic formulations (check label or pharmacy instructions).
- Protect from direct sunlight or extreme temperatures.
- Sterility
- Use sterile, unexpired products. Do not reuse needles or syringes.
- Dispose of injection materials in approved sharps containers.
9. Adverse Event Reporting
- Severe Reactions
- If you experience any severe or life-threatening symptoms, discontinue use and seek emergency medical care.
- FDA Reporting
- You or your healthcare provider can report suspected adverse reactions to the FDA’s MedWatch Program at 1-800-FDA-1088 or online at www.fda.gov/medwatch.
10. Disclaimer
- Not Evaluated by the FDA
- These statements have not been evaluated by the FDA, and MIC+B12 injections are not approved to diagnose, treat, cure, or prevent any disease beyond recognized indications.
- Consult a Professional
- This information is intended for educational purposes only and does not replace professional medical advice.
- Individual Variation
- Responses to lipotropic injections vary; results are not guaranteed. Always follow healthcare professional guidance regarding dosage, follow-ups, and any complementary dietary or lifestyle adjustments.
Questions or Concerns?
If you have any questions about Lipotropic (MIC) and B12 injections, including their potential benefits, side effects, or dosage, please consult your qualified healthcare provider.
Methylcobalamin (Vitamin B12) Injection: Important Safety Information
1. Introduction
- What Is Methylcobalamin?
Methylcobalamin is a biologically active form of Vitamin B12. It is often prescribed or administered to individuals with Vitamin B12 deficiency, or for certain neurological and hematological conditions. - Regulatory Status
In some cases, compounded forms of methylcobalamin have not been evaluated or approved by the U.S. Food and Drug Administration (FDA) for all potential uses. If you prefer or require an FDA-approved product, please consult your healthcare provider for alternatives.
2. Potential Benefits & Uses
- Common Indications
- Treating or preventing Vitamin B12 deficiency (e.g., pernicious anemia).
- Providing support for neurological health in certain conditions (e.g., peripheral neuropathy).
- Assisting with red blood cell formation and overall energy metabolism.
- Limitations
While many individuals benefit from methylcobalamin injections, this product is not intended to diagnose, treat, cure, or prevent any disease beyond uses recognized by healthcare professionals. Always consult your provider to determine if this therapy is right for you.
3. Contraindications
You should not receive methylcobalamin injections if:
- You have a known allergy or hypersensitivity to Vitamin B12, cobalt, or any ingredient in the formulation.
- You have Leber’s disease (hereditary optic nerve atrophy), as high-dose B12 supplementation could potentially worsen the condition.
- You are pregnant or breastfeeding without first discussing risks and benefits with your healthcare provider.
4. Warnings & Precautions
- Not FDA-Approved for All Uses
- Certain forms or dosages of methylcobalamin may be compounded and not specifically reviewed by the FDA.
-
- Consult a Healthcare Professional
- Inform your provider about your medical history, including any allergies, kidney or liver disease, or blood disorders.
- Discuss any other medications or supplements you are taking, as these may interact with B12 therapy.
-
- Pre-Existing Conditions
- Use caution if you have a history of hematological disorders, as your provider may require regular lab work (e.g., complete blood counts).
-
- Use in Specific Populations
- Safety in pregnant or nursing women has not been fully established for high-dose methylcobalamin.
- Pediatric use should be supervised by a qualified medical professional.
5. Potential Side Effects
While most people tolerate methylcobalamin injections well, side effects can occur. Contact your healthcare provider if you experience any of the following symptoms, especially if they are severe or persistent:
- Injection Site Reactions
- Redness, swelling, tenderness, or mild pain at the injection site.
- If signs of infection (e.g., warmth, pus, significant redness) develop, seek medical attention.
-
- Allergic Reactions
- Itching, rash, hives, swelling of the face/lips/tongue, or difficulty breathing.
- If you experience these signs, discontinue use and seek emergency medical care.
-
- Gastrointestinal Symptoms
- Nausea, diarrhea, or upset stomach may occur.
- Report severe or persistent gastrointestinal issues to your provider.
-
- Dizziness or Headache
- Some individuals may experience mild dizziness or headaches.
- If severe, stop use and consult a healthcare professional.
-
- Hypokalemia (Low Potassium)
- Very rarely, rapid improvement in anemia can cause shifts in potassium levels.
- Symptoms might include muscle weakness, irregular heartbeat, or confusion. Inform your provider if you experience these.
6. Drug Interactions
- Medication and Supplement Considerations
- Metformin, proton pump inhibitors, and other drugs can affect or be affected by B12 status.
- Always inform your healthcare provider of all medications (prescription and over-the-counter), vitamins, or herbal supplements you are taking.
7. Administration & Dosage
- Administration Method
- Typically administered intramuscularly (IM) or subcutaneously (SQ).
- Should be administered by a qualified healthcare professional or according to instructions provided by your medical team.
-
- Dosage
- Dosage and frequency vary based on individual needs (e.g., underlying deficiency, condition severity).
- Follow your provider’s directions precisely. Do not adjust the dose without medical guidance.
-
- Monitoring
- Periodic blood tests (e.g., serum B12 levels, complete blood counts) may be recommended to ensure the therapy is effective and safe.
8. Storage & Handling
- Temperature
- Store as indicated by your pharmacist or on the product label (often refrigerated or at controlled room temperature).
- Sterility
- Use only sterile, unexpired products.
- Do not reuse needles or syringes; dispose of them in approved sharps containers.
9. Adverse Event Reporting
- Immediate Care
- If you experience severe side effects (e.g., difficulty breathing, significant swelling, severe pain), seek immediate medical attention.
- FDA Reporting
- You or your healthcare provider can report suspected adverse reactions to the FDA’s MedWatch Program at 1-800-FDA-1088 or online at www.fda.gov/medwatch.
10. Disclaimer
- Not Evaluated by the FDA for All Uses
- These statements may not be reviewed by the FDA, and methylcobalamin injections are not FDA-approved to diagnose, treat, cure, or prevent any disease beyond recognized indications.
- Consult a Professional
- This information is for educational purposes only and does not replace medical advice, diagnosis, or treatment from a qualified healthcare provider.
- Individual Variation
- Treatment response and side effects may vary. Always follow the advice of your healthcare professional regarding therapy, dosage, and monitoring.
Questions or Concerns?
If you have any questions regarding methylcobalamin (Vitamin B12) injections, including their potential benefits, side effects, or dosage, please consult a qualified healthcare professional.
Join 100,000+ patients feeling their best
“I have been with this company for over a year and their customer service is above and beyond. I appreciate the sincere and kind representatives.”
All your questions, answered
What if I need to cancel?
Absolutely! We understand that circumstances may change, and there are no long-term contracts or cancellation fees involved. We are committed to customer satisfaction.
Do I need insurance?
No, IVY RX does not require insurance. We keep things simple with transparent pricing, straightforward billing, and affordable generic options—making it easier than ever to take care of yourself.
Can I talk to a doctor?
Absolutely! You can quickly and securely message your care providers through our patient portal. Simply log in, choose your provider, and send them a message. It’s that easy!
Who are the healthcare providers?
All IVY RX affiliated doctors are board certified US-licensed healthcare professionals. The medical advisory board comprises experts in psychology, oncology, men's health, sexual health, neurology, and family medicine. Learn more about our medical advisory board here.
How are compounded medications sourced?
The treatments are compounded in pharmacies compliant with 503B/USP <797> standards. This ensures a high level of quality and safety throughout the entire process.
Don’t just live longer,
live healthier
Start your 5-minute assessment and receive your medication in as little as 2 days
