LAVOMAX ® (Tilorone)


Buy Tilorone Dihydrochloride tablets with the fastest delivery!

Lavomax is an immunomodulating and antiviral drug intended for the treatment and prevention of respiratory and other viral diseases.

Tilorone, its active ingredient, stimulates the production of interferons (proteins essential for anti-viral defense) and enhances immunity during influenza and ARVI. The synthesis method and antiviral properties of tilorone were first patented in 1968 in the USA. In USSR the production and use of this drug started in 1975.

Research demonstrated that Lavomax is effective in treating viral infections, including influenza and other acute respiratory viral infections, hepatitis and herpes, cytomegalovirus, and neurotropic viruses. The drug inhibits viral translation in the infected cells and prevents the spread of viruses, thus showing a strong antiviral effect.

Pharmacodynamic properties

Lavomax stimulates the production of alpha, beta, and gamma types of interferons in intestinal epithelial cells, hepatocytes, T-cells, and neutrophils.

It also contributes to the growth of bone marrow cells and enhances antibody production, stabilizes the level of immunosuppression, and regulates the T-Lymphocyte Helper/Suppressor ratio.

You can buy Tilorone dihydrochloride tablets for use as a part of complex therapy of:

  • Influenza and ARVI;
  • Herpes;
  • Prevention of influenza and ARVI;
  • The drug can also be used as part of complex therapy of viral hepatitis A, B, and C, cytomegalovirus infection, and non-gonococcal urethritis.


Produced by Stada / Nizhfarm, Russia.

Read more about immunostimulants.


Active ingredient: tilorone dihydrochloride 125 mg;
Inactive ingredients: magnesium hydroxycarbonate, povidone K30, and calcium stearate.


  • Hypersensitivity to tilorone and other components of the drug;
  • Pregnancy and lactation;
  • Children under 18 years of age;
  • Sucrase-isomaltase deficiency, fructose intolerance, or glucose-galactose malabsorption (the drug contains sucrose).


Dosage and administration

To be administered orally after meals. 1 tablet per day during the first 2 days, then 1 tablet once every 2 days.

The maximum dose for influenza and ARVI treatment course is 750 mg (6 tablets). The maximum dose for herpes and other viral infections treatment course is 1.25–2.5 mg (10–20 tablets).

Side effects

Allergic response, dyspepsia, and short-term chills.


No cases of overdose were recorded.

Drug interaction

The drug can be co-administered with antibiotics and medicines treating viral and bacterial diseases. No significant drug interactions were recorded.

Storage conditions

Store in a dark place at a temperature not higher than 25°C (77°F). Keep out of the reach of children.
Shelf life is 2 years.


Stada / Nizhfarm, Russia.

  1. Glaz et al (1973) Antiviral Activity and Induction of Interferon-Like Substance by Quinacrine and Acranil
  2. Levine et al (1975) Nuclear bodies produced in astrocytes by tilorone
  3. Kuehne et al (1977) Evaluation of Various Analogues of Tilorone Hydrochloride Against Venezuelan Equine Encephalitis Virus in Mice
  4. Donahoe et al (1977) In vivo function tests of the effect of tilorone and niridazole on cell-mediated immunity in chickens
  5. Kavetskiĭ et al (1977) Tilorone, a synthetic immunostimulator possessing antitumor activity
  6. Cummings et al (1981) Phase II trials of Baker’s antifol, bleomycin, CCNU, streptozotocin, tilorone, and 5-fluorodeoxyuridine plus arabinosyl cytosine in metastatic breast cancer
  7. Y Hiyama, K Kuriyama et al (1991) Dissociation between antiinflammatory action of tilorone and its interferon inducing activity
  8. Selkova et al (2001) Effect of amyxin–a domestic analog of tilorone–on characteristics of interferon and immune status of man
  9. Briggs et al (2008) α7 nicotinic acetylcholine receptor agonist properties of tilorone and related tricyclic analogues
  10. Ratan et al (2010) Small Molecule Activation of Adaptive Gene Expression. Tilorone or Its Analogs Are Novel Potent Activators of Hypoxia Inducible Factor-1 That Provide Prophylaxis against Stroke and Spinal Cord Injury
  11. Schrimpf et al (2012) SAR of α7 nicotinic receptor agonists derived from tilorone: exploration of a novel nicotinic pharmacophore
  12. Leppäranta et al (2013) Bone morphogenetic protein-inducer tilorone identified by high-throughput screening is antifibrotic in vivo
  13. Wissing et al (2014) Small-molecule screening of PC3 prostate cancer cells identifies tilorone dihydrochloride to selectively inhibit cell growth based on cyclin-dependent kinase 5 expression
  14. Ekins et al (2018) Efficacy of Tilorone Dihydrochloride against Ebola Virus Infection
  15. Vartiainen et al (2018) Pulmonary administration of a dry powder formulation of the antifibrotic drug tilorone reduces silica-induced lung fibrosis in mice

Related products

Triazavirin® is an antiviral drug. It is the first medicine in the azoloazine group. It's said to be effective against 15 strains of influenza and fevers, including swine and avian ones as well as some dangerous pathogenic viruses. Triazavirin is used in case of exacerbations of bronchial asthma caused by viral infections. The instructions say that the drug inhibits the synthesis of the virus RNA and the replication of fragments of its genome. Thus, it does not allow the virus to produce its copies in the affected cell.



Naltrexone® is an opioid antagonist. It is primarily used to manage alcohol or opioid dependence. It reduces the effect of opioid analgesics and eliminates side effects of opioids (including endogenous ones). In alcoholism, it binds to opioid receptors and blocks the effects of endorphins. Low dose of Naltrexone (LDN) is recommended by some doctors for the use in HIV/AIDS, cancer, autoimmune diseases, and central nervous system disorders. Fast US domestic shipping is available.



Licopid® (or Lycopid) is an immunomodulator containing a complete synthetic analogue of natural GMDP or glucosaminyl muramyl dipeptide. Once in the body, Lycopid mimics the natural process of detecting fragments of peptidoglycan bacteria. Thus, the effect of the drug is as close as possible to the process of natural immunoregulation.

Heptor® is a drug based on ademetionine (S-Adenosyl methionine), which is currently considered one of the most powerful hepatoprotectors. Besides, ademetionine also has anti-inflammatory, painkiller and antidepressant effects. Heptor is a choleretic and cholekinetic drug. The use of the drug in patients with osteoarthritis helps relieve pain and stimulate proteoglycan synthesis and cartilage tissue regeneration. Fast US domestic shipping is available.