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Adipotide
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AOD-9604
Weight Management
BPC-157
Healing & Recovery
Cagrilintide
Weight Management
CJC-1295
Growth Hormone
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Sleep & Recovery
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NAD+
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Hormone Support
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Recovery
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Retatrutide
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Selank
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Semax
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Snap-8
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SS-31
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TB-500
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Tesamorelin
Growth Hormone
Thymosin Alpha-1
Immune
Tirzepatide
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Total Peptides: 32
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Immune Protocol

ImunofanComplete Dosing & Administration Guide

Synthetic hexapeptide derived from thymopoietin with immunomodulatory, antioxidant, and hepatoprotective properties

Dose Range

50-100mcg

Frequency

Once daily

Route

Subcutaneous injection

Cycle Length

8-12 weeks

Dosing

How much
do I take?

Starting Dose

50 mcg subcutaneously or intramuscularly every other day

Frequency

Every other day

Duration

5-15 injections per course (10-30 days)

Standard injection protocol uses 1 mL of 0.005% solution (50 mcg) administered subcutaneously or intramuscularly every other day. A typical course consists of 10-15 injections. For chronic infections and cancer adjuvant therapy, courses may be repeated after a break.

Standard Dose

50 mcg per dose, one spray in each nostril once daily

Frequency

Once daily

Duration

10-15 days per course

Intranasal administration provides a non-invasive route with good mucosal absorption. One spray delivers 50 mcg. Convenient for patients who prefer to avoid injections or for maintenance therapy after an initial injection course.

Advanced Dose

100 mcg once daily

Frequency

Once daily

Duration

10-20 days per course

Rectal suppositories contain 100 mcg of active ingredient — double the injection dose to compensate for absorption differences. Used when injection and intranasal routes are not suitable, particularly in pediatric populations or patients with needle aversion.

Timing

Best time to take

Administer Imunofan at the same time each day (or on the same day each week for weekly injections). Many users prefer morning or evening administration. Pick a time you'll remember consistently.

With food?

Imunofan injections can be given regardless of meal timing. However, if GI effects occur, administering on an empty stomach or with a light meal may help reduce discomfort.

If stacking

Imunofan should be used as directed by your healthcare provider. If combining with other medications or supplements, discuss potential interactions with your provider. Avoid combining with compounds that have overlapping mechanisms unless specifically guided by a medical professional.

Adjusting Your Dose

Increase if

  • +Your healthcare provider determines that a longer course (beyond 15 injections) is needed based on immune parameter monitoring
  • +You are undergoing extended chemotherapy and need sustained immune support
  • +Your condition involves severe immunodepression requiring more intensive treatment

Decrease if

  • -You experience persistent injection site reactions — consider switching to nasal spray or suppository form
  • -You show signs of excessive immune activation (fever, malaise)
  • -Your immune parameters have normalized and maintenance rather than intensive therapy is appropriate

Signs of right dose

  • Noticeable improvement in target symptoms
  • Good tolerance with minimal side effects
  • Consistent positive response between doses
  • Improved lab markers or clinical assessments (if applicable)

Dosing Calculator

Calculate Your Exact Dose

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Step 1: Peptide Weight

Find the weight printed on your peptide vial label

Look here!

The weight is on the label

Peptide vial
5mg

Select Weight

mg

Look for a number followed by 'mg' on the vial label (e.g., 5mg, 10mg)

Administration

How do I
use it?

Reconstitution

What you need

  • Imunofan vial (lyophilized powder or solution)
  • Bacteriostatic water or sterile sodium chloride for reconstitution
  • Alcohol swabs for cleaning vial tops and injection sites
  • Appropriately sized syringes with fine-gauge needles (27-30 gauge)
  • Sharps disposal container

Example

Add the recommended volume of bacteriostatic water to the Imunofan vial. Gently swirl (do not shake) until the powder is fully dissolved. The resulting solution should be clear. Calculate your individual dose based on the concentration and your prescribed amount.

Your dose of Imunofan is determined by your healthcare provider. Using an insulin syringe marked in units, draw up the exact amount prescribed. For example, if the reconstituted concentration is 1mg/mL and your dose is 0.5mg, draw up 0.5mL (50 units on an insulin syringe). Always double-check calculations before injection.

Injection

Route

Subcutaneous injection (into the fatty tissue just under the skin)—allows for consistent absorption and can be self-administered at home after proper training

Best sites

  • Abdomen (stomach area)—at least 2 inches from the belly button, most popular choice for self-injection
  • Front of thighs—middle to upper portion of the outer leg
  • Back of upper arm—outer area (may need assistance from another person)

Technique

  • 1.Wash your hands thoroughly with soap and water before handling supplies
  • 2.Clean the injection site with an alcohol swab and let it air dry completely
  • 3.Pinch a fold of skin at the chosen injection site
  • 4.Insert the needle at a 45-90 degree angle (depending on needle length and body composition)
  • 5.Inject the medication slowly and steadily over 5-10 seconds
  • 6.Release the skin fold and remove the needle, applying gentle pressure with a clean swab
  • 7.Rotate injection sites to prevent tissue irritation or lipodystrophy
  • 8.Dispose of the needle safely in a sharps container—never recap or reuse needles
Full Injection Guide

Storage

Before reconstitution

Store Imunofan in the refrigerator at 36-46°F (2-8°C) in its original packaging. Protect from light and moisture. Do not freeze. Check the expiration date before use. Some formulations may be stored at room temperature for limited periods—check your specific product labeling.

After reconstitution

Once reconstituted, Imunofan should be kept refrigerated at 36-46°F (2-8°C) and used within the timeframe specified on your product labeling (typically 14-28 days). Label the vial with the reconstitution date. Do not use if the solution appears cloudy, discolored, or contains particles.

Signs of degradation

  • Solution appears cloudy, discolored, or contains visible particles (should be clear)
  • Product has been exposed to temperatures outside the recommended storage range
  • Product has been frozen (unless specifically designed for freeze-thaw stability)
  • Expiration date has passed or reconstituted solution has exceeded its use-by date
  • Unusual odor, color change, or visible contamination

Sample Daily Schedule

As prescribed (once daily)

As prescribed by your healthcare provider injection

Site: Subcutaneous injection—rotate sites if applicable

Maintain a consistent schedule for optimal results with Imunofan. Set reminders if needed. If you miss a dose, follow your healthcare provider's instructions—do not double up on doses to compensate.

Safety

Is it
safe?

Safety Profile

Imunofan (Iletin-alpha, a synthetic tetrapeptide) demonstrates good tolerability in Russian clinical practice spanning 20+ years with oral and parenteral administration. Immunomodulatory peptides carry theoretical risks of over-stimulating autoimmune responses, but Imunofan safety data show no increased autoimmune flare rates in patients with existing autoimmune conditions. Injection site reactions and mild fever (1-3% of users) are the documented adverse events, not immunotoxicity. The mechanism of enhanced T-cell maturation appears selective and safe at therapeutic doses.

Imunofan safety is supported by post-market surveillance in Russia and Eastern Europe involving thousands of patients with immunodeficiency, cancer, and chronic infection. Published trials in Russian journals show stable white blood cell counts and no worsening of autoimmune disease activity at standard doses. While not FDA-approved in the US, the peptide's structural simplicity and lack of systemic toxicity signals (hepatic, renal, cardiac) support its use as an immune support agent in research settings.

Common Side Effects

Experienced by some users

Injection site reaction

Mild redness, tenderness, or slight swelling at the subcutaneous or intramuscular injection site. This is the most commonly reported side effect and is typically transient.

Management: Rotate injection sites between administrations. Apply a cold compress if needed. Reactions typically resolve within 24 hours.

Transient headache

Mild headache may occur within the first few hours after administration, particularly during the initial fast-phase antioxidant response.

Management: Usually self-resolving within a few hours. Standard analgesics may be used if needed. Tends to diminish with subsequent doses.

Nasal irritation (intranasal form)

Brief stinging, itching, or irritation in the nasal passages after intranasal spray administration. May include temporary bitter taste.

Management: Normal and transient — resolves within minutes. If persistent irritation occurs, consider switching to injection or suppository form.

Transient mild fever

Low-grade temperature elevation may occur as part of the immune activation process, particularly during the middle phase of action when phagocytic responses increase.

Management: Monitor temperature. Usually resolves within 24 hours without intervention. Antipyretics may be used if uncomfortable.

Mild fatigue

Some patients report mild fatigue or drowsiness in the hours following administration, likely related to the immune rebalancing process.

Management: Rest as needed. This effect typically diminishes over the course of treatment as the immune system normalizes.

Gastrointestinal discomfort (suppository form)

Mild rectal irritation or abdominal discomfort may occur with suppository use, particularly during the first few administrations.

Management: Ensure proper insertion technique. If discomfort persists, consider switching to intranasal or injection route.

Less Common

  • Allergic reaction

These typically resolve with continued use or dose adjustment.

Stop and Seek Help If

  • ×Severe or worsening side effects that don't improve with dose adjustment or supportive care
  • ×Signs of an allergic reaction—rash, hives, swelling, or difficulty breathing
  • ×Your healthcare provider recommends discontinuation based on your clinical response
  • ×Development of any new medical condition that may be contraindicated with Imunofan
  • ×Pregnancy or planning to become pregnant (unless specifically approved for use during pregnancy)
  • ×Abnormal lab results or clinical markers that suggest adverse effects

Imunofan should only be started, adjusted, or discontinued under medical supervision. This information is for educational purposes only and does not replace professional medical advice. Never stop a prescribed treatment without consulting your healthcare provider first, as abrupt discontinuation may have consequences.

Interactions

With other peptides

  • Both derive from thymic peptide pathways and share immune-enhancing mechanisms. Combination may be synergistic but could lead to excessive immune activation. Use together only under medical supervision.
  • Closely related — both are derived from thymopoietin. Imunofan is a modified version of TP-5's parent molecule. Combined use is likely redundant rather than harmful, but not typically recommended.
  • Complementary mechanisms — BPC-157 focuses on tissue repair while Imunofan provides immune modulation and antioxidant support. No known negative interactions.

With medications

  • Chemotherapy drugs - Imunofan is specifically designed for adjunctive use with chemotherapy. It reduces toxic and radiation reactions while its inhibition of drug resistance proteins may enhance chemotherapy effectiveness. Used together under oncologist supervision.
  • !Immunosuppressants (cyclosporine, tacrolimus) - Imunofan's immune-restoring effects may counteract the intended immunosuppression. Avoid concurrent use or use only with careful medical monitoring.
  • Antiviral medications (hepatitis treatment) - Imunofan is commonly used alongside antiviral therapy for hepatitis B and C, with complementary mechanisms — antivirals target the virus while Imunofan restores immune function and protects the liver.
  • Corticosteroids - High-dose systemic corticosteroids may partially counteract Imunofan's immune-enhancing effects. However, Imunofan has been used in settings involving steroid resistance, suggesting potential complementary mechanisms.

With supplements

  • N-Acetyl Cysteine (NAC) - Both have antioxidant properties. Combining may provide additive antioxidant protection. No known negative interactions.
  • Vitamin C - Complementary antioxidant support. Vitamin C may enhance the antioxidant fast-phase effects of Imunofan. Safe to combine.
  • Selenium - Selenium supports the antioxidant enzyme system and may complement Imunofan's redox-balancing effects. No known negative interactions.
  • Zinc - Zinc supports immune cell function and may enhance Imunofan's immune-restorative effects. Commonly used together in clinical practice.

Want the Full Picture?

View the complete Imunofan research profile including mechanism of action, clinical studies, effectiveness timeline, and FAQ.

View Full Imunofan Profile

Medical Disclaimer

Imunofan is an investigational research compound not approved by the FDA for human therapeutic use. This information is for educational purposes only and should not be construed as medical advice. Always consult with a qualified healthcare provider before starting any new supplement or treatment protocol.

Last updated: 2/8/2026