Product image of Helixor P (Liquid Extract From Viscum Album Subsp. Austriacum Var Pinus Sylvestris (1:20), Extraction Solvents:) supplied by GNH India

Helixor P

Active Ingredient:
Liquid Extract From Viscum Album Subsp. Austriacum Var Pinus Sylvestris (1:20), Extraction Solvents:
Origin:
EU

Helixor P (Liquid Extract From Viscum Album Subsp. Austriacum Var Pinus Sylvestris (1:20), Extraction Solvents:)

Helixor P is a prescription‑only injectable solution that contains a liquid extract of Viscum album subsp. austriacum var. pinus sylvestris (mistletoe) prepared at a 1:20 ratio with extraction solvents. The product is supplied as a sterile subcutaneous preparation and is marketed in the European Union for use under medical supervision. Helixor P is classified as a herbal extract with immunomodulatory and antineoplastic properties. It is administered by a qualified professional.

Manufacturer / TM Owner

Helixor Heilmittel Gmbh

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Indications & Clinical Uses

Helixor P is used as an adjunctive therapy in oncology, primarily to support patients undergoing conventional cancer treatments and to address therapy‑related symptoms.

  • As an adjunct to chemotherapy, radiotherapy, or surgery for various solid tumors.
  • To help alleviate treatment‑related fatigue, weight loss, and reduced appetite.
  • For potential enhancement of immune response during cancer therapy.
  • As part of supportive care aimed at improving patients’ quality of life.
  • In palliative settings where disease control is limited but symptom management is needed.

Side Effects

Side‑effect profiles for Helixor P reflect its biologically active mistletoe constituents and are reported from clinical observations; most reactions are mild and reversible, while rare serious events require medical attention.

Common

  • Mild injection‑site reactions such as redness, swelling, or tenderness.
  • Transient flu‑like symptoms including fever, chills, or headache.
  • Temporary increase in heart rate or mild hypertension.
  • Nausea or mild gastrointestinal discomfort.
  • Local skin irritation or pruritus at injection site.

Serious

  • Allergic reactions ranging from urticaria to anaphylaxis.
  • Significant hypotension or cardiovascular instability.
  • Hepatic enzyme elevations indicating liver stress.
  • Severe leukopenia or neutropenia observed in rare cases.

Precautions & Warnings

When prescribing Helixor P, clinicians should evaluate patient history and monitor for specific safety considerations.

  • Contraindicated in patients with known hypersensitivity to mistletoe extracts.
  • Use caution in individuals with autoimmune disorders or chronic inflammatory conditions.
  • Not recommended during pregnancy or lactation due to insufficient safety data.
  • Baseline and periodic assessment of blood pressure and heart rate is advisable.
  • Monitor liver function tests during prolonged therapy.
  • Evaluate for potential interactions with immunosuppressive agents.
  • Adjust dosage or discontinue if severe adverse reactions occur.

Avoid Interactions

Helixor P may influence the activity of certain medications; awareness of possible interactions helps ensure safe combined use.

Avoid

  • Concurrent use with high‑dose immunosuppressants such as cyclosporine or tacrolimus.

Use with caution

  • Combination with chemotherapy agents; monitor for enhanced toxicity.
  • Concurrent administration of anticoagulants; observe for changes in bleeding risk.
  • Use with other herbal preparations that affect immune function.
  • Co‑administration with beta‑blockers; watch for additive cardiovascular effects.
  • Concomitant use with vaccines; assess timing to avoid immune interference.

Frequently Asked Questions

Helixor P contains a liquid extract of Viscum album subsp. austriacum var. pinus sylvestris, a mistletoe plant, prepared at a 1:20 ratio with extraction solvents.

Helixor P is supplied as a sterile injectable solution intended for subcutaneous injection by a qualified health professional.

It is used as an adjunctive treatment for cancer and as supportive care to help manage symptoms related to oncology therapies.

No, Helixor P is a prescription‑only medication and must be prescribed by a licensed healthcare provider.

There is insufficient safety data for use in pregnancy or lactation, so it is generally not recommended for pregnant or nursing individuals.

Common reactions include mild injection‑site redness or swelling, flu‑like symptoms such as fever or chills, temporary increases in heart rate, and mild gastrointestinal discomfort.

Serious events may include allergic reactions up to anaphylaxis, significant hypotension, hepatic enzyme elevations, and rare cases of leukopenia or neutropenia.

Yes, baseline and periodic monitoring of blood pressure and heart rate is advisable because the product can affect cardiovascular parameters.

Helixor P may interact with high‑dose immunosuppressants, certain chemotherapy agents, anticoagulants, beta‑blockers, other immune‑modulating herbs, and vaccines; caution and monitoring are recommended.

Helixor P is marketed in the European Union and is not currently approved by the U.S. Food and Drug Administration.

Regular assessment of liver function tests, blood pressure, heart rate, and observation for any adverse reactions are recommended during extended treatment.

Published by

GNH India Pharmaceuticals Limited

Licensed pharmaceutical supplier

Last updated:

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