Product image of Methoxsalen G.L. Pharma (Methoxsalen) supplied by GNH India

Methoxsalen G.L. Pharma

Active Ingredient:
Methoxsalen
Origin:
EU

Methoxsalen G.L. Pharma (Methoxsalen)

Methoxsalen, the active ingredient in Methoxsalen G.L. Pharma, is a psoralen (furocoumarin) presented as a pharmaceutical preparation for extracorporeal use. It is employed in photochemotherapy to treat vitiligo and psoriasis in patients requiring controlled UVA exposure.

GNH India supplies Methoxsalen G.L. Pharma as a licensed, GDP‑compliant international pharmaceutical supplier serving hospitals, pharmacies and clinics worldwide.

Manufacturer / TM Owner

G.L. Pharma Gmbh

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Indications & Clinical Uses

Methoxsalen is used in photochemotherapy for disorders of skin pigmentation and proliferation.

  • Vitiligo: promotes repigmentation of depigmented skin areas when combined with UVA therapy.
  • Psoriasis: reduces plaque formation and scaling through controlled UV‑A exposure.
  • PUVA therapy: acts as the photosensitising agent that enables UVA to exert therapeutic effects.

How It Works

  • Methoxsalen intercalates between DNA base pairs and, upon activation by UVA radiation, forms covalent cross‑links with pyrimidine residues. These DNA adducts inhibit DNA synthesis and cell proliferation while also exerting local immunosuppressive effects, thereby modulating abnormal skin cell growth and pigment cell activity.

Side Effects

Methoxsalen may cause a range of adverse reactions, ranging from mild to severe.

Common Side Effects

  • Nausea: mild to moderate upset stomach.
  • Headache: transient cranial discomfort.
  • Erythema: redness of skin at treated sites.
  • Pruritus: itching following UVA exposure.
  • Phototoxic reactions: heightened skin sensitivity to light.
  • Vomiting: occasional emesis after dosing.

Serious or Rare Side Effects

  • Severe phototoxic burns: extensive skin injury after UVA.
  • Hepatic dysfunction: abnormal liver enzyme elevations.
  • Hemolytic anemia: destruction of red blood cells, especially in G6PD deficiency.
  • Bone marrow suppression: reduced blood cell production.
  • Cardiac arrhythmias: irregular heart rhythms in susceptible individuals.
  • Severe nausea/vomiting: persistent gastrointestinal distress requiring medical attention.

Precautions & Warnings

Methoxsalen requires careful patient assessment and monitoring before and during therapy.

  • Pregnancy: avoid use unless benefits clearly outweigh potential risks.
  • Breastfeeding: contraindicated due to unknown excretion in milk.
  • Contraindications: do not use in patients with porphyria or systemic lupus erythematosus.
  • UV exposure: limit uncontrolled sunlight to prevent unexpected phototoxicity.
  • Liver function: monitor hepatic enzymes regularly during treatment.
  • Store at below 25°C: keep in original packaging, protect from moisture and direct light.

Avoid Interactions

Methoxsalen can interact with other medications, altering its safety profile.

Major Interactions (Avoid)

  • Azathioprine: increased risk of bone marrow suppression.
  • Oral retinoids (e.g., acitretin): heightened phototoxicity.
  • Other photosensitising agents: additive skin sensitivity.

Moderate Interactions (Monitor Closely)

  • Antifungal agents (e.g., itraconazole): may affect methoxsalen metabolism.
  • Hormonal contraceptives: potential reduction in contraceptive efficacy.

Frequently Asked Questions

Methoxsalen G.L. Pharma is employed in photochemotherapy, primarily for the treatment of vitiligo and psoriasis. It acts as a photosensitising agent in PUVA (psoralen + UVA) therapy, helping to restore skin colour in vitiligo and to reduce plaque formation in psoriasis.

Methoxsalen intercalates into DNA and, when activated by UVA light, creates covalent cross‑links with pyrimidine bases. This blocks DNA synthesis, suppresses abnormal cell proliferation, and modulates local immune responses, which together produce the therapeutic effects seen in PUVA treatment.

The specific dose of methoxsalen is determined by the prescribing clinician based on the patient’s condition, weight, and response to therapy. Dosage regimens are individualized and should follow the prescriber’s instructions and local treatment protocols.

Safety data for methoxsalen in pregnancy and lactation are limited. It is generally advised to avoid use during pregnancy unless the potential benefit justifies the risk, and it is contraindicated while breastfeeding because of unknown excretion in milk.

To place an order, submit an enquiry on the product page at gnhindia.com, specifying the required quantity. GNH India works with hospitals, pharmacies and procurement teams worldwide, verifies trade or institutional credentials, and then provides pricing, availability, shipping details and any necessary import documentation.

Methoxsalen is the most widely used psoralen for PUVA therapy due to its well‑characterised pharmacokinetic profile and established efficacy. Alternative psoralens exist, but methoxsalen offers a balance of potency and safety that makes it the standard choice in many dermatology centres.

Methoxsalen should be stored at temperatures below 25 °C, in its original container, protected from moisture and direct light. Maintaining these conditions helps preserve its stability and potency throughout its shelf life.

Methoxsalen is administered extracorporeally, typically as an oral dose taken a few hours before a controlled UVA exposure session. The exact timing and amount are prescribed by the treating physician to align with the planned phototherapy schedule.

Serious risks include severe phototoxic burns, hepatic dysfunction, hemolytic anemia (especially in G6PD‑deficient individuals), and bone‑marrow suppression. Patients should be monitored closely for these events, and therapy should be discontinued if any serious adverse reaction occurs.

Methoxsalen is contraindicated in patients with porphyria, systemic lupus erythematosus, or a known hypersensitivity to psoralens. It should also be avoided in individuals taking other strong photosensitising drugs without careful medical supervision.

Published by

GNH India Pharmaceuticals Limited

Licensed pharmaceutical supplier

Last updated:

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