Tigason

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Tigason

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Medically reviewed

Marina Burgos

Last updated on 10/01/2026

This page provides general, reference-level information compiled from official medical sources. It is not a substitute for professional medical advice, diagnosis, or treatment. For decisions about your health, please consult a qualified healthcare professional.

Overview of Tigason

Property Description
Active ingredient Etretinate (INN)
Form Oral capsules (Hard gelatin)
Pharmacological class Retinoid; Systemic anti-psoriatic agent
Common use Management of severe, chronic skin disorders
Origin Synthetic derivative of Vitamin A

What is Tigason (Etretinate) and Its Chemical Identity?

Tigason is the trade name for a prescription-only medication whose active component is Etretinate, which is classified as a synthetic aromatic retinoid. This potent substance is a synthetic derivative chemically related to Vitamin A, designed for systemic administration. Etretinate is a second-generation retinoid, a chemical class known to modify cellular processes. Its distinctive feature is its exceptionally long biological half-life, a property that substantially informed subsequent pharmacological development. This prolonged retention in the body differentiates its therapeutic profile from other retinoids, ultimately leading to its replacement by its active metabolite, Acitretin (Soriatane).

Pharmacological Class and General Therapeutic Purpose

Tigason is fundamentally categorized as a systemic anti-psoriatic agent, recognized for its function as a powerful anti-keratinization agent. The drug's general purpose is to provide internal, systemic regulation for severe, chronic, and stubborn skin disorders characterized by pathological cell growth. Etretinate is clinically recognized for its ability to correct the hyperproliferation of skin cells in recalcitrant conditions. The therapeutic utility stems from its ability to directly influence cellular processes, specifically by normalizing the differentiation and maturation of skin cells. This means the medication acts to correct the rapid and abnormal turnover of skin cells, helping to achieve effective control over extensive symptoms, such as scaling and thickening, in adults with severe dermatoses.

What is the Composition and Drug Form of Tigason?

Tigason is supplied as an oral preparation in hard gelatin capsules, intended to be taken by mouth for absorption into the bloodstream. The composition confirms Etretinate as the single-component active ingredient. Since the molecule is highly lipophilic (fat-soluble), the formulation utilizes excipients within the capsule, often including lipids, which are necessary to ensure the drug is efficiently absorbed and distributed throughout the body to initiate its required systemic therapeutic action.

Regulatory References

  1. Acitretin (Soriatane) Drug Information

What side effects are possible with Tigason?

Safety-Related Restrictions and Monitoring

The primary safety concern documented in regulatory sources is the extreme teratogenicity of Tigason (etretinate), which causes severe congenital disabilities. As the drug and its metabolite can persist in the body, women of childbearing potential are subject to a mandatory pregnancy prevention program that requires highly effective contraception during treatment and for a specified period (up to three years) after the drug is stopped. Alcohol consumption must also be strictly avoided during and for two months after treatment due to the risk of the drug converting into a longer-lasting, teratogenic metabolite.

Common and Serious Adverse Reactions

The most frequent adverse reactions are typically mucocutaneous and often dose-dependent, including chapped lips (cheilitis), dry skin, scaling/peeling of skin (especially on palms/soles), hair loss, and dry eyes.

Serious or clinically significant adverse reactions documented by regulatory bodies involve key organ systems and require monitoring:

  • Hepatotoxicity: Liver enzyme elevation, hepatitis, or cirrhosis can occur. Regular liver function tests are mandated.
  • Metabolic Effects: Increases in blood lipids (triglycerides and cholesterol) are common and can be severe, requiring routine blood tests and caution in patients with pre-existing hyperlipidemia or diabetes.
  • Skeletal Changes: Long-term use may lead to bone and joint abnormalities, such as diffuse skeletal hyperostosis, necessitating periodic assessment.
  • Ophthalmic Effects: Decreased night vision has been reported, requiring caution when driving or operating machinery in low light. Benign intracranial hypertension (pseudotumor cerebri), which presents with severe headache, nausea, and visual changes, is a rare but serious adverse reaction and is an absolute contraindication when used with tetracyclines.

Blood donation is prohibited during treatment and for up to three years after discontinuation due to the risk of a pregnant recipient being exposed to the teratogen.

Overdose and Emergency Response

Overdose and When to Seek Help — Official Regulatory Information for Tigason

Overdose Scope

Overdose with high doses of Tigason (etretinate) may result in a condition known as retinoid poisoning, which is similar to Vitamin A intoxication (hypervitaminosis A syndrome).

Documented Overdose Presentations: Clinical manifestations of an overdose are known to affect the Central Nervous System and the skin. These symptoms may include sedation, headache, irritability, papilloedema (swelling of the optic disk), and a generalised peeling of the skin.

Dose-Related Factors: Acute toxicity is associated with high doses. In cases of prolonged overdose, the drug’s accumulation in fat tissue can contribute to toxic effects. If a prolonged overdose occurs in a child, growth may be permanently arrested.

Required Emergency Actions

When to Seek Immediate Medical Help: In all cases of suspected overdose, it is necessary to get medical help or contact a Poison Control Center right away.

Procedural Instructions: If the medicine has been swallowed, do NOT induce vomiting. If vomiting occurs spontaneously, the individual should be positioned (such as leaning forward or on their left side) to help maintain an open airway and prevent aspiration.

Therapeutic Uses of Tigason

Tigason's active ingredient, Etretinate, is relevant for the management of severe skin disorders.

Systemic Control of Severe, Recalcitrant Psoriasis

Tigason is commonly used to help with the management of severe and extensive forms of chronic psoriasis in adults, including highly symptomatic types like erythrodermic and generalized pustular psoriasis. It is applied in clinical settings where the disease is recalcitrant (stubbornly resistant) to other therapeutic approaches. This provides systemic support that may assist with easing the symptom burden and supports general well-being during symptomatic phases.

Management of Pathological Skin Thickening and Dyskeratoses

The medication is relevant for treating conditions characterized by disordered skin cell growth, specifically severe disorders of keratinization (dyskeratoses). This includes challenging conditions such as Ichthyosis, Darier’s disease, and Pityriasis Rubra Pilaris. Tigason is used for managing symptom clusters like excessive scaling and severe skin thickening (hyperkeratosis), which may assist with easing distress associated with these difficult, chronic manifestations.


Quick Facts: Therapeutic Focus

  • Tigason is relevant for easing symptoms related to pathological skin thickening and widespread scaling in severe dermatoses.
  • It supports the management of chronic conditions presenting with widespread, disfiguring skin manifestations.

Eligibility and Restrictions for Use

Tigason (acitretin) is a retinoid medication typically reserved for severe skin disorders resistant to other treatments, such as extensive psoriasis and certain forms of congenital ichthyosis. Its use is limited to patients for whom the potential benefits are judged to outweigh the significant risks.


Absolute Contraindications (Do Not Use)

This medication is strictly contraindicated in several groups due to the high risk of severe adverse effects:

  • Pregnancy and women of childbearing potential: Tigason is a powerful teratogen (causes severe birth defects). Women must not be pregnant during treatment or for three years after stopping therapy and must use two effective forms of contraception during this entire period. They must also abstain from alcohol during treatment and for two months after, as alcohol can convert acitretin into a highly persistent teratogenic substance.
  • Breastfeeding mothers
  • Severe liver or kidney impairment
  • Chronic, abnormally elevated blood lipid (triglyceride/cholesterol) values
  • Hypersensitivity or allergy to acitretin, other retinoids, or Vitamin A
  • Concomitant use with other medications, including methotrexate (due to increased risk of liver toxicity), tetracycline antibiotics (due to risk of increased intracranial pressure), or other Vitamin A/retinoid supplements (due to risk of hypervitaminosis A).

Precautions for Use

Caution is required for patients with pre-existing conditions, including diabetes mellitus, hyperlipidemia, obesity, or a history of depression or other mental health conditions. Regular monitoring of liver function and blood lipids is essential during treatment.

What should I know about interactions with other medicines?

Tigason (acitretin) can interact with a variety of medications and substances, potentially leading to serious adverse effects or reduced effectiveness of one or both products. It is essential to inform your healthcare provider of all prescription drugs, over-the-counter medicines, vitamins, and herbal supplements you are taking.

Contraindicated Combinations

  • Tetracycline Antibiotics: The concurrent use of Tigason with tetracyclines (such as minocycline or doxycycline) is contraindicated, as both drug classes can increase the risk of developing pseudotumor cerebri (benign intracranial hypertension).
  • Methotrexate: Combining Tigason with methotrexate significantly increases the risk of hepatotoxicity (liver damage). This combination should be avoided.

Other Significant Interactions

  • Alcohol (Ethanol): Tigason should not be taken with alcohol. Alcohol can lead to the formation of etretinate, a related retinoid that has a significantly longer half-life and extends the duration of potential teratogenic effects (risk of birth defects) for women of child-bearing potential to beyond three years. Women must abstain from all forms of alcohol during and for at least two months after treatment.
  • Progestin-Only Contraceptives: Tigason may interfere with the effectiveness of low-dose, progestin-only birth control pills (the "mini-pill"). Reliable alternative or additional non-hormonal contraception must be used.
  • Vitamin A Supplements: The simultaneous use of Tigason and large doses of vitamin A or other oral retinoids (e.g., isotretinoin) can increase the risk of retinoid-related side effects.

Mechanism of Action

Receptor Agonism and Gene Transcription

Tigason's primary action is exerted by its active metabolite, acitretin, which functions as an agonist by binding to nuclear Retinoic Acid Receptors (RARs) and Retinoid X Receptors (RXRs) inside keratinocytes. This binding creates a complex that regulates gene transcription, modulating the genetic instructions that dictate cellular behavior and contributing to the modulation of epithelial growth processes across affected tissues.

Modulation of Keratinocyte Proliferation and Differentiation

The modulation of gene transcription directly influences the Keratinocyte Differentiation and Proliferation Pathways. This action involves the reduction of keratinocyte proliferation and the induction of terminal differentiation, influencing the overall rate and sequence of cell turnover. These cellular changes result in a modulation of epidermal architecture and the sequence of cell detachment.

⏳ Constraint by Slow Transcriptional Cascade

The entire mechanistic process is constrained by its dependence on the slow biochemical cascade of gene regulation, which requires time for new proteins to be synthesized and accumulated in the cell. This inherent limitation in the mechanism explains why the physiological adjustment to the tissue structure becomes observable gradually over a period of weeks.

Dosage and Administration Information

Official Administration Guidelines for Tigason (Acitretin)

Tigason is an oral capsule formulation taken once daily and must be swallowed whole. To ensure optimal absorption, the capsule should be taken with a meal or a glass of milk. Dosage is highly individualized and is determined by a physician based on the patient’s clinical response and tolerability.

Dosing Schedule

Administration Scope Details (Adults)
Route of Administration Oral capsule
Initial Daily Dose Typically 25 mg to 50 mg for 2 to 4 weeks
Maintenance Daily Dose Adjusted based on response, generally 25 mg to 50 mg. The lowest effective dose should be used for long-term disorders of keratinization, often not exceeding 50 mg/day.
Timing Once daily, with food or milk

Mandatory Procedural Conditions

Strict adherence to the following conditions is required for all patients, particularly for females of childbearing potential, due to the severe risk of birth defects (teratogenicity) associated with the drug:

  • Contraception (Females): Two effective forms of contraception must be used simultaneously for at least one month prior to therapy, during therapy, and for a minimum of three years after the final dose. Treatment must start on the second or third day of the next normal menstrual period.
  • Alcohol Restriction (Females): Ingestion of alcohol or alcohol-containing products must be strictly avoided during treatment and for two months following treatment cessation. Alcohol promotes the formation of a metabolite with a significantly longer half-life, extending the teratogenic risk.
  • Missed Dose: If a dose is missed, skip the missed dose and resume the regular dosing schedule; do not take a double dose.
  • Blood Donation: Patients must not donate blood during treatment and for at least three years after stopping Tigason, as the blood could be given to a female of childbearing potential.

Recent Clinical Evidence

Tigason (Acitretin): Recent Clinical Evidence

Tigason is the brand name for the retinoid acitretin, a medication primarily used for severe, resistant forms of psoriasis and certain inherited disorders of keratinization, such as ichthyosis. Clinical evidence confirms its utility, often classifying it as an established second-line systemic treatment.

Efficacy in Psoriasis

Clinical trials routinely measure the drug's effect using the Psoriasis Area and Severity Index (PASI) score. In studies of severe chronic plaque-type psoriasis, treatment with acitretin has been observed to lead to significant reductions in the PASI score. For instance, in various trials, a PASI 75 response (indicating a 75% or greater improvement in severity) was achieved by approximately 45% to 69% of adult patients after 12 weeks of therapy, with results often varying by dose and specific patient cohort. The onset of observed improvement typically begins around four to six weeks, with maximum benefit potentially requiring three to four months.

Acitretin is particularly noted for its use in pustular and erythrodermic variants of psoriasis. It is also frequently utilized in combination therapy with phototherapy (e.g., PUVA or UVB) or other systemic agents, as it is generally considered to lack the significant immunosuppressive effects of some alternatives.

Use in Keratinization Disorders

For inherited disorders of keratinization, such as lamellar ichthyosis, acitretin remains a mainstay of systemic therapy. Studies have noted that the treatment may result in a reduction of hyperkeratosis (skin thickening and scaling), helping to normalize keratinocyte differentiation. Dosage adjustments are often critical in managing long-term treatment and tolerability in this patient group.

How should Tigason be stored and disposed of?

How to Store and Dispose of Tigason (Acitretin)

The official storage requirements for this medication, which is commonly marketed as its active metabolite, acitretin, are strictly defined to maintain stability and potency.

Condition Regulatory Requirement
Temperature Store at Controlled Room Temperature (20 C to 25 C).
Protection Must be kept in the original, tightly closed container and protected from light, moisture, and freezing.
Child Safety Store out of the sight and reach of children.

Disposal instructions mandate that unused or expired capsules must not be thrown away with household trash or wastewater. All surplus medication should be returned to a pharmacist for appropriate pharmaceutical waste disposal, according to local government regulations.

Attention! Always consult to a doctor or pharmacist before using pills or medicines.

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