Thymalin

Thymalin scored 5.1 / 10 (⚖️ Neutral) on the BioHarmony scale as a Substance → Peptide → Immune Peptide.

Thymalin is a bovine-thymus peptide extract studied for immune restoration and aging, scoring 5.1 (Neutral). Its strongest claim, a 2 to 4 fold elderly mortality drop per Khavinson 2003, is real but single-source and never independently replicated in the West.

Overall5.1 / 10⚖️ NeutralContext-dependent
Your Score🔒Take the quiz →
Immune Function 4.2 Longevity / Lifespan 4.0 Geriatric / Aging Population 2.6 Anti-Inflammatory 2.5 Healthspan 2.4
📅 Scored May 23, 2026·BioHarmony v1.0·Rev 2

What is Thymalin?

Thymalin is a peptide extract pulled from calf thymus, and the most important thing to know up front is that it is a mixture, not a single molecule. It is a fraction of many thymic peptides of different lengths, characterized and put into Russian clinical use as an immunocorrector by the Morozov 1997 and Khavinson group. It comes from Vladimir Khavinson's peptide-bioregulator program, where it has been used for decades to restore immune function and studied for aging. It lands at Neutral (5.1) for one reason: the science is genuinely intriguing but the entire human case rests on a single research lineage.

Here's the part that makes thymalin worth a look. Long-term elderly-cohort work from the Khavinson group reported large mortality drops, roughly 2 to 4 fold, and a recent trial reported a severe-COVID survival benefit, per Khavinson 2003. And here's the cap that defines the whole report: that evidence is single-source, mostly non-blinded, often old, and has zero independent Western replication, and the biggest numbers are large enough to be suspicious on their own. It is also a bovine biological given by injection courses and sold grey-market, which adds sourcing concerns a defined synthetic peptide would not carry. So the promise is real, and so is the reason to stay skeptical.

Terminology

A few terms decide how you read this report, because thymalin gets confused with its better-defined cousins constantly, and because the gap between an interesting signal and a proven one is exactly where it lives.

  • Thymalin: A bovine-thymus peptide extract, a mixture of thymic peptides, used as an immunocorrector. The subject of this report.
  • Immunocorrector: The Russian clinical term for an agent meant to restore or rebalance immune function rather than simply suppress or stimulate it.
  • Peptide bioregulator: Khavinson's framing for short peptides that he proposes can re-enter cells, reach the nucleus, and adjust gene expression to restore tissue function.
  • Single-source evidence: Findings that all trace back to one research group, with no independent team reproducing them. The defining limitation here.
  • Bovine biological: A product derived from cow tissue. It carries sterility, endotoxin, batch-consistency, and theoretical bovine-tissue concerns that a synthetic molecule avoids.
  • IM: Intramuscular, an injection into muscle. Thymalin's only real route of administration.
  • CD28: A surface marker of mature T lymphocytes. Its rise in cell culture is read as a push toward T-cell maturation.
  • KE and EW: The dipeptides Vilon (Lys-Glu) and the basis of Thymogen (Glu-Trp), short peptides isolated or designed from the parent extract.

How do you take Thymalin?

Dosing & Protocols

Dosing information is summarized from published research and community reports. This is not a prescribing guide. Consult a healthcare provider before starting any protocol.

View 1 route and 3 protocols

Routes & Forms

RouteFormClinical RangeCommunity Range
Intramuscular injectionLyophilized powder reconstituted with sterile or bacteriostatic water About 5 to 10 mg per day for 5 to 10 day courses (Russian clinical use) 5 to 20 mg per day for 5 to 10 days, repeated 1 to 2 times per year

Protocols

Standard immune course (Russian clinical pattern) Clinical

Dose
5 to 10 mg
Frequency
Once daily
Duration
5 to 10 consecutive days

The classic immunocorrector course used in the Russian literature. Repeated as cycles rather than run continuously. Not an approved dose.

Longevity-protocol cadence Anecdotal

Dose
5 to 10 mg
Frequency
Once daily during a course
Duration
5 to 10 day courses, repeated 1 to 2 times per year

Mirrors the cohort study design, where bioregulators were given only in the first 2 to 3 years yet differences were reported across a longer window. Often run inside the broader Russian bioregulator stack with Epitalon.

Higher community course Anecdotal

Dose
10 to 20 mg
Frequency
Once daily
Duration
5 to 10 days

Some longevity guides cite higher daily amounts. There is no controlled human study supporting the larger range, and a bigger dose of an undefined extract is not obviously better.

How the score is calculated
Upside (weighted)
+1.83
Downside (harm ×1.4)
1.78
EV = 1.831.78 = 0.05 Score = ((0.05 + 7) / 12) × 10 = 5.1 / 10

What are the benefits of Thymalin?

Upside contribution: 1.83

DimensionWeightScoreVisualWeighted
Efficacy25%3.2
0.800
Breadth15%3.2
0.480
Evidence25%2.2
0.550
Speed10%3.0
0.300
Durability10%2.5
0.250
Bioindividuality15%3.0
0.450
Total2.830

Upside Rationale

The upside is concentrated in a coherent, decades-deep immune-restoration story with one genuinely striking human outcome, the elderly mortality drop. Thymalin's real asset is a consistent direction across immune, respiratory, and aging endpoints, plus a mechanism that points toward T-cell maturation. Its ceiling is set entirely by where that evidence comes from: a single research lineage with no outside replication. Breadth and efficacy score moderately because the reported effects are large and span systems. Evidence is the dimension that holds the total down hardest, on purpose.

Efficacy (3.2/5.0): Efficacy is moderate because the reported effects are large but cannot be taken at face value. The flagship 266-person elderly cohort reported mortality falling roughly 2 to 4 fold over 6 years, with acute respiratory disease incidence down 2.0 to 2.4 fold, per Khavinson 2003. A severe-COVID trial reported hospital mortality of about 20.6 percent with thymalin versus 40.9 percent for basic care, per Kuznik 2022. Those are big numbers. The reason efficacy does not score higher is that the magnitude itself is a flag for an undefined extract studied by one group, and a 4 fold mortality drop is the kind of result that demands outside confirmation before it earns a high mark.

Breadth of Benefits (3.2/5.0): Breadth is moderate because thymalin's reported effects span several systems, even if each is thinly evidenced. The literature touches immune function, respiratory illness including ARDS and severe COVID, per Linkova 2023, cardiovascular hemodynamics, per Cherkashin 2002, and aging endpoints. The boundary is that breadth of claim is not breadth of proof. Every one of these domains is documented by the same program, usually in small or non-blinded work, so the wide reach reads as a coherent theory applied across systems rather than independent confirmation in each. That is enough for a moderate mark, not a strong one.

Evidence Quality (2.2/5.0): Evidence quality is the binding constraint and the reason this report sits at Neutral rather than higher. The problem is not a lack of papers, it is that all of them come from one research lineage. Every iteration of the headline mortality result traces to the Khavinson and St. Petersburg group, per Khavinson 2003, the work reads as observational follow-up rather than registered blinded trials, the core data is from the 1990s, and there is zero independent Western replication of thymalin specifically. Unlike the defined peptide thymosin alpha-1, which has multiple independent multicenter trials, thymalin's human outcomes have never been reproduced outside the program that created them. That single-source, unreplicated, mostly unblinded, often old profile is precisely why this dimension scores low, and it would rise to roughly 3.0 if an independent group reproduced the results.

Speed of Onset (3.0/5.0): Speed is a relative bright spot. Thymalin is given as a course over days, and immune-marker shifts are reported within a single treatment cycle, with lymphocyte and monocyte counts roughly doubling and inflammatory markers falling during COVID adjunct use, per Khavinson 2021. So the biological response, at least as measured by blood markers, appears to move on the timescale of a course rather than months. The caveat is that these onset readouts come from the same single-source literature, so the speed claim carries the same uncertainty as the efficacy claim it sits next to.

Durability (2.5/5.0): Durability is the most attractive design feature and also one of the least verified. The defining trait of the cohort work is that bioregulators were given only in the first 2 to 3 years of a 6 to 8 year follow-up, yet mortality and morbidity differences were reported across the full window, per Khavinson 2003. That implies lasting benefit from short pulsed courses, which is why longevity protocols use repeated annual or semiannual cycles rather than daily dosing. There is no documented withdrawal or rebound. The score stays mid-range because this persistence claim is itself part of the single-source evidence and has not been independently confirmed.

Bioindividuality Upside (3.0/5.0): Response should vary in a fairly predictable direction. The whole program targets the immunosenescent elderly, people with declining T-cell output who have the clearest mechanistic reason to respond, and the human cell work points toward restoring T-cell maturation, per Khavinson 2020. That gives a clear responder profile: older adults with weakened immunity stand to gain more than young, healthy people. The reason this does not score higher is that an undefined extract with batch-to-batch variability and no validated biomarker to predict response limits how confidently anyone can forecast who benefits.

What are the risks & downsides of Thymalin?

Downside contribution: 1.78 (safety risks weighted extra)

DimensionWeightScoreVisualWeighted
Safety30%2.6
0.780
Side effects15%2.2
0.330
Cost5%2.8
0.140
Effort5%3.2
0.160
Opportunity5%3.0
0.150
Dependency15%2.3
0.345
Reversibility25%1.8
0.450
Total2.355
Harm subtotal × 1.42.667
Opportunity subtotal × 1.00.450
Combined downside3.117
Baseline offset (constant)−1.340
Effective downside penalty1.777

Downside Rationale

The downside is dominated by uncertainty and sourcing, not by an intrinsic dangerous pharmacology. Thymalin is reported as well tolerated across decades of Russian use, with no fatal signal in that literature, so the molecule itself is not the main worry. The heavier weight falls on the injection-course effort, the cost of repeated cycles, and the genuine opportunity cost of choosing an unreplicated extract over a better-defined option. The sterility and contamination concern is real but lives in the Verdict as a sourcing issue, since it is about how the product is made and sold, not about the compound's own biology.

Safety Risk (2.6/5.0): Safety risk is moderate and driven by unknowns rather than a confirmed dangerous effect. Thymalin is reported as well tolerated across four decades of Russian clinical use, with no intrinsic life-threatening signal in the literature reviewed, per Khavinson 2020. The molecule class itself is not acutely hazardous. What keeps the score from being lower is that there is no Western pharmacovigilance, no adverse-event file, and no post-market surveillance, because the product is not approved in those jurisdictions, so an absence of reported harm partly reflects an absence of monitoring. The sterility and contamination concerns that come with a bovine biological are real but extrinsic, a property of grey-market sourcing rather than the compound, so they weigh in the Verdict rather than inflating this dimension.

Side Effect Profile (2.2/5.0): Side effects are reported as minimal across the Russian literature, with no notable adverse profile attached to standard courses, per Morozov 1997. The most plausible real-world issues are local: injection-site reactions and, because this is a bovine protein, the possibility of an allergic response in a sensitized person. The score is low, reflecting a clean reported profile, with the honest caveat that the reporting comes from the originating program rather than independent surveillance, so rare effects could be undercounted. It is worth separating two things here. The thymalin molecule, as studied, does not appear to produce a meaningful side-effect burden, which is what this dimension measures. The contamination and sterility risks that come with a grey-market bovine injectable are a different category, a function of how the product is sourced rather than what the compound does, and those belong in the Verdict. Keeping the two apart is the only honest way to score an extract that looks clean in the lab but ships through an unregulated supply chain.

Financial Cost (2.8/5.0): Cost is moderate and recurring. Grey-market vials of thymalin are not individually expensive, but the protocol is course-based and repeated periodically, so a year of cycles plus the markup on an imported research compound adds up. The relevant framing is not the price of one vial but the ongoing spend on repeated courses of an unproven extract. There is a hidden cost too: because thymalin is an undefined mixture, a careful buyer would want third-party testing on each batch, and that verification is rarely available for grey-market biologicals, so the practical choice is to either pay for testing that does not exist or accept unknown quality. Neither is cheap in the sense that matters.

Time/Effort Burden (3.2/5.0): Effort is meaningful. Thymalin requires reconstituting a lyophilized powder, drawing it up, and giving an intramuscular injection daily across a multi-day course, then repeating those courses on a schedule. That is a real logistics and adherence load compared with an oral supplement, and intramuscular self-injection is a higher bar than the subcutaneous shots many peptide users are used to. Sterile technique, proper storage of a reconstituted biological, and site rotation all add friction, and the course-then-repeat cadence means the effort never fully ends the way a finished bottle of capsules does. For anyone not already comfortable injecting, the learning curve alone is a deterrent worth weighing before starting.

Opportunity Cost (3.0/5.0): Opportunity cost is genuine because a better-defined option exists for the same goal. Anyone reaching for thymalin to support immune function is choosing an undefined, single-source extract over Thymosin Alpha-1, a defined peptide with independent multicenter trials. Money, effort, and the willingness to inject a grey-market biological could instead go to that better-supported peptide, or to the sleep, training, and nutrition basics that move immune resilience with far more certainty. That trade-off is the main reason to think twice.

Dependency/Withdrawal (2.3/5.0): Dependency risk is low. Thymalin is used in pulsed courses, not continuous daily dosing, and there is no documented addiction, tolerance, rebound, or downregulation in the literature. The cohort design itself, dosing only in the early years yet reporting effects later, argues against any need to stay on it. The small amount of risk reflected here is functional reliance on repeat courses to sustain a claimed benefit, not a withdrawal syndrome. If anything, the bigger pull is psychological: a longevity protocol can become a habit you keep paying for and injecting because stopping feels like giving up an edge, even when the underlying evidence never proved the edge existed. That is a behavior pattern to watch in yourself, not a pharmacological dependency the compound creates.

Reversibility (1.8/5.0): Reversibility is excellent and one of thymalin's cleaner attributes. It is course-based and clears from the body after a cycle, with no documented withdrawal, taper requirement, or lasting structural change. If you stop, you simply stop, and the claimed effects fade rather than leaving a residue you have to manage. That clean exit is a genuine point in its favor, and it lowers the stakes of trying it: a peptide that washes out cleanly is far less worrying than one that locks in a change you cannot undo. The main exception would be an allergic sensitization to the bovine protein, which is a reaction rather than a lingering pharmacological effect, but it is the one outcome that does not simply reverse on stopping.

Is Thymalin worth it?

Thymalin sits at Neutral because it pairs a genuinely intriguing, decades-deep immune-restoration signal, headlined by the 2 to 4 fold elderly mortality drop in Khavinson 2003, with an evidence base that no independent group has ever confirmed, wrapped in a grey-market bovine injectable. If you are drawn to the Khavinson bioregulator program, understand that the entire human case is single-source and unreplicated, can verify a clean source, and treat thymalin as an experiment rather than a proven therapy, it is a reasonable thing to explore. If you want defined, Western-trialed evidence behind your immune support, the data is not there, and a better-characterized option carries far less uncertainty. The two biggest real-world frictions are the unverifiable sourcing of a bovine biological and the injection-course burden.

Best for: Researchers and longevity enthusiasts fascinated by the Khavinson peptide-bioregulator program who want to explore its immune pillar firsthand. Older adults with declining immune function, the population with the clearest mechanistic reason to respond. People who fully accept that the human evidence is single-source and unreplicated and will judge thymalin on their own response rather than the headline numbers. Anyone who can source a clean, properly handled bovine-derived injectable and is comfortable with intramuscular course dosing. Users who treat it as a once-or-twice-a-year experiment inside a broader stack, not a proven staple.

Avoid if: You want defined, independently trialed evidence, since thymalin's human results have never been reproduced outside one program. You cannot verify sterility and source quality, because a grey-market bovine biological carries contamination, endotoxin, and theoretical bovine-tissue concerns that the molecule's own safety record does not cover. You have any active or suspected cancer, where immune and growth-axis modulation is best avoided without specialist guidance. You have a known sensitivity to bovine proteins, given the allergic-reaction risk. You are uneasy with intramuscular self-injection or with running an unapproved compound at all.

What is Thymalin best for?

The overall BioHarmony score reflects the intervention's primary evidence profile. These subratings are independent assessments per use case.

Use CaseScoreSummary
○ Immune Function Primary4.2Immune function is thymalin's strongest and oldest claim, and the reason it was put into clinical use in Russia as an immunocorrector, per Morozov 1997. In human hematopoietic stem cell culture it raised the mature T-cell marker CD28 by about 6.8 fold and cut stem-cell markers 2 to 3 fold, per Khavinson 2020. The score stays below a top mark because the entire human immune case traces to one research lineage, with no independent Western confirmation of the crude extract and no modern blinded trials of immune outcomes in healthy people.
○ Longevity / Lifespan Primary4.0Longevity is the most eye-catching claim and the weakest-supported. The flagship 266-person elderly cohort reported mortality falling roughly 2 to 4 fold over 6 years, per Khavinson 2003. That is an extraordinary result for an undefined extract, and it is single-source: every version of it traces to the same St. Petersburg group with no independent replication. The score reflects a real, internally consistent signal that cannot be trusted at face value until another group reproduces it outside the originating program.

Frequently Asked Questions

What is thymalin, and is it a single peptide?

Thymalin is a peptide extract from calf thymus, a mixture of many thymic peptides rather than one defined molecule, per Morozov 1997. That is the central distinction: it is the parent extract, and the defined short peptides like KE (Vilon) and EW (Thymogen) were isolated or designed from it. A common vendor error labels thymalin a 2 to 4 amino acid ultrashort peptide, which is false and a sourcing red flag, since thymalin is the crude mixture, not a single sequence.

What does the Khavinson elderly-mortality data show, and can I trust it?

The flagship 266-person elderly cohort reported mortality dropping roughly 2 to 4 fold over 6 years, per Khavinson 2003. Trust it cautiously. The result is internally consistent and spans decades, but it is single-source: every version traces to the same St. Petersburg group, the design reads as observational rather than a registered blinded trial, the core data is from the 1990s, and no independent Western group has reproduced it. A 4 fold drop from an undefined extract is large enough that the size itself is a reason for caution.

Did thymalin help in severe COVID-19?

One Russian trial reported severe-COVID hospital mortality of about 20.6 percent with thymalin added to standard care, versus 40.9 percent for basic therapy and 28.4 percent for tocilizumab, per Kuznik 2022. It also reported faster declines in IL-6, CRP, and D-dimer, per Khavinson 2021. Treat it as suggestive, not settled: the same paper's two language abstracts disagree on the exact mortality figure, the work is small, and it comes from the same single research family with no independent replication.

How is thymalin different from thymosin alpha-1 and thymulin?

Thymalin is an undefined bovine-thymus extract, while Thymosin Alpha-1 is a single 28-amino-acid peptide with independent multicenter trials, and thymulin is a defined endogenous thymic nonapeptide. The practical difference is evidence and definition: thymosin alpha-1 is the better-studied, better-characterized option, which is why it scores higher in this report set. Thymalin is the historical Russian parent extract, intriguing but single-source. If you want a defined molecule with Western trials behind it, thymalin is not it.

Is thymalin safe, and what about its bovine source?

Thymalin is reported as well tolerated across four decades of Russian use, with no intrinsic fatal signal in that literature, per Khavinson 2020. The bigger concern is sourcing, not the molecule. Because it is a bovine biological made and sold outside any Western regulator, sterility, endotoxin, batch consistency, and a theoretical bovine-tissue concern all apply, and self-injected grey-market material adds contamination risk. Absence of a Western adverse-event file means absence of monitoring, not proven safety. Verify the source carefully.

How is thymalin dosed?

Reported protocols use about 5 to 10 mg per day by intramuscular injection for 5 to 10 consecutive days, repeated as periodic courses, per Khavinson 2003. Some longevity guides cite up to 10 to 20 mg per day. None of this is an approved dose. Thymalin is an injected lyophilate reconstituted with sterile water, not an oral product, and the course-then-repeat pattern mirrors the cohort design where dosing happened only in the first few years. The injection and cycling burden is real compared with an oral supplement.

Who is thymalin for, and who should skip it?

Thymalin is best framed as a research-grade experiment for people drawn to the Khavinson bioregulator program who fully accept that its human case is single-source and unreplicated, per Khavinson 2003. Skip it if you want defined, Western-trialed evidence, if you cannot verify a clean bovine-derived injectable, if you have any active cancer, or if you are uneasy injecting a grey-market biological. For most people chasing immune support, a better-defined option like Thymosin Alpha-1 carries less uncertainty.

How does thymalin fit into the Russian bioregulator stack?

Thymalin is positioned as the immune pillar of the Khavinson peptide-bioregulator program, often run alongside the pineal peptide Epitalon and others like Cortexin or Vilon. The cohort even reported a larger mortality drop for the thymalin-plus-pineal combination than either alone, per Khavinson 2003. The same caveat applies to the stack as to the single agent: the combination data is single-source and unreplicated, so the appealing synergy story should be held loosely rather than treated as proven.

What could change Thymalin's score?

BioHarmony scores are living assessments. New research, regulatory changes, or personal context can shift the score up or down. These are the most likely scenarios that would change this intervention's rating.

The fastest path up is the one thing thymalin has never had: independent replication. A blinded trial from a research group outside the Khavinson program reproducing even a fraction of the immune or mortality signal would lift Evidence and Efficacy together and move thymalin toward worth trying. The fastest path down is a credible safety signal or a clean failure to replicate. Because the score rests almost entirely on single-source evidence, any real outside data, in either direction, would move it more than usual. This is the unusual case where the bottleneck is not the size of the reported effect, which is already large, but who is allowed to confirm it. Until a second team weighs in, every scenario below hinges on that single missing piece, which is why even modest outside evidence carries outsized weight here.

ScenarioDimension shiftsNew Score
An independent Western group replicates the immune or mortality signal in a blinded trialEvidence 2.2 to 3.4, Efficacy 3.2 to 3.75.6 / 10 ⚖️ Neutral
A registered modern trial confirms the severe-COVID survival benefitEvidence 2.2 to 2.9, Breadth 3.2 to 3.65.4 / 10 ⚖️ Neutral
The extract is fully characterized and standardized for batch consistencyBioindividuality 3.0 to 3.6, Safety 2.6 to 2.35.3 / 10 ⚖️ Neutral
A serious contamination or allergic-reaction pattern emerges from grey-market productSafety 2.6 to 3.6, Side effects 2.2 to 3.04.5 / 10 ⚖️ Neutral
An attempted replication fails to beat control for a headline claimEfficacy 3.2 to 2.4, Evidence 2.2 to 1.84.8 / 10 ⚖️ Neutral
Better-defined thymic peptides keep outperforming it in head-to-head useOpportunity 3.0 to 3.6, Efficacy 3.2 to 2.84.9 / 10 ⚖️ Neutral
Thymalin's flagship claim is one of the largest in the longevity-peptide literature: a 266-person elderly cohort where mortality fell roughly 2 to 4 fold over 6 years. The catch is that it has never been reproduced outside the group that ran it. Source: Khavinson 2003, Neuro Endocrinol Lett
In human stem-cell culture, thymalin raised the mature T-cell marker CD28 by about 6.8 fold, the cleanest mechanistic hint for its immune claims. It is also why the molecule, separate from its sourcing, has no intrinsic fatal signal. Source: Khavinson 2020, Bull Exp Biol Med

Key Evidence Sources

What does the evidence say about Thymalin?

Evidence on this intervention is summarized across three complementary streams: contemporary clinical research, pre-RCT-era pharmacology and observational use, and the traditional medical systems that documented it first. Convergence across streams signals higher confidence; divergence is surfaced honestly.

Modern Clinical Research

Confidence: Low

Modern evidence for thymalin is unusual: abundant in volume, decades deep, internally consistent, and almost entirely from one research lineage. The flagship human result is a 266-person elderly cohort reporting mortality roughly 2 to 4 fold lower over 6 years, per Khavinson 2003, with a recent severe-COVID trial reporting hospital mortality of about 20.6 percent versus 40.9 percent for basic care, per Kuznik 2022. Human cell work shows a push toward T-cell differentiation, per Khavinson 2020, and the extract was characterized as an immunocorrector long ago, per Morozov 1997. The decisive problem: this is single-source work, mostly non-blinded, often old, with zero independent Western replication of thymalin, and the largest effect sizes are suspiciously big for the design. There is no documented traditional-medicine lineage, since thymalin is a 20th-century laboratory extract, so no historical or traditional lens applies.

Citations: Khavinson 2003, Kuznik 2022, Khavinson 2020, Morozov 1997

What to Track If You Try This

These are the data points that matter most while running a 30-day Experiment with this intervention.

How to read this section
Pre
Test or score before starting the protocol. Anchors a baseline.
During
Track while running the protocol so you can see if anything is changing.
Post
Re-test after a full cycle to confirm the change held.
Up
The marker should rise. For most positive outcomes, that is a good sign.
Down
The marker should fall. For most positive outcomes, that is a good sign.
Stable
The marker should hold steady. Big swings in either direction are a yellow flag.
Watch
Direction depends on dose, timing, and your baseline. Pay close attention to the trend.
N/A
No expected direction. The entry is there to anchor a baseline reading.
Primary
The Pulse dimension most likely to shift. Track this first.
Secondary
Also relevant, but a smaller or less consistent shift. Track if Primary is unclear.

Bloodwork to Order

Open These Markers In Your Dashboard

  • Cbc Pre | Expected Watch During | Expected Up
  • CRP During | Expected Down
  • D Dimer During | Expected Watch

Pulse Dimensions to Watch

  • Energy During | Expected Up | Primary
  • Body During | Expected Watch | Secondary
  • Calm During | Expected Watch | Tertiary

Subjective Signals (Daily Voice Card)

  • Frequency and length of colds or minor infections Scale 1-5 | During | Expected Down
  • Injection-site redness, swelling, or any allergic reaction Scale 1-5 | During | Expected Watch

Red Flags: Stop and Consult

  • Any allergic reaction to a bovine biological, including hives, swelling, or trouble breathing: stop immediately and seek care.
  • Injection-site infection, spreading redness, warmth, or pus: stop and consult a clinician, since grey-market sterility is unverifiable.
  • Any active or suspected cancer: do not use without oncology guidance; immune and growth-axis modulation is best avoided.
  • Product labeled as a 2 to 4 amino acid ultrashort peptide: that is a mislabeling red flag, since thymalin is the parent extract, not a short peptide.

Other interventions for Immune Function

See all ratings →
📊 How BioHarmony scoring works

BioHarmony translates a weighted expected-value calculation into a reader-facing 0–10 score. Tier bands: Skip 0–3.6, Caution 3.7–4.7, Neutral 4.8–5.7, Worth Trying 5.8–6.9, Strong Recommend 7.0–7.9, Top-tier 8.0+.

Harm-type downsides (safety risk, side effects, reversibility, dependency) carry a 1.4× precautionary multiplier. Harm weighs more than benefit. Opportunity-type downsides (financial cost, time/effort, opportunity cost) are subtracted at face value.

Use case subratings are independent assessments of how well the intervention addresses specific health goals. They are not components of the overall score. Each subrating reflects the scorer's judgment based on use-case-specific evidence, safety, and effect sizes.

Every dimension is evaluated on a 1–5 scale, and the baseline (1) is subtracted before weighting. A perfect intervention with zero downsides contributes zero penalty rather than a residual floor, so top-tier scores are actually reachable.

EV = Upside − Downside
EV = 1.830 − 1.777 = 0.053
Formula v0.5 maps EV = 0 to score 5.0. Above neutral, 1 EV point equals 1 score point. Below neutral, 1 EV point equals about 0.71 score points, so EV = −7 reaches 0.0 while EV = +5 reaches 10.0. Both sides use the full 5-point half-scale.
Score = 5 + (0.053 / 5) × 5 = 5.1 / 10

See the full BioHarmony methodology →

This report is educational and informational. It is not medical advice, diagnosis, or treatment. Consult a qualified healthcare provider before starting any new supplement, device, protocol, or intervention, particularly if you take prescription medications, have a chronic health condition, are pregnant or nursing, or are under 18.