Product image of Hemangiol (Propranolol Hydrochloride) supplied by GNH India

Hemangiol

Active Ingredient:
Propranolol Hydrochloride
Origin:
EU

Hemangiol (Propranolol Hydrochloride)

Hemangiol is an oral solution containing propranolol hydrochloride, a non‑selective beta‑adrenergic antagonist, marketed in the European Union. The medication is supplied by prescription and is formulated for pediatric and adult use. Hemangiol’s strength is not publicly specified, and it is administered by mouth. It belongs to the beta blocker class and works by blocking beta‑adrenergic receptors, affecting heart rate and angiogenesis through the vascular pathways.

Manufacturer / TM Owner

Pierre Fabre Medicament

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Indications & Clinical Uses

Hemangiol is prescribed for several cardiovascular and vascular conditions, especially in infants and children, where beta‑blockade can reduce lesion growth and control blood pressure.

  • Infantile hemangioma – treatment of proliferating cutaneous or visceral lesions in patients younger than one year.
  • Essential hypertension – adjunctive therapy when monotherapy does not achieve target blood pressure in pediatric or adult patients.
  • Cardiac arrhythmias – management of supraventricular tachycardia or other rhythm disturbances requiring rate control.
  • Post‑surgical hemangioma recurrence – prophylactic use to lower risk of regrowth after excision.
  • Off‑label migraine prophylaxis – occasional use under specialist supervision for chronic migraine prevention.

Side Effects

The safety profile of Hemangiol reflects the typical effects of non‑selective beta‑blockers, with most patients experiencing mild, transient symptoms that often resolve without intervention. Monitoring is recommended during dose adjustments.

Common

  • Fatigue or tiredness.
  • Dizziness, especially when standing quickly.
  • Cold extremities or reduced peripheral circulation.
  • Gastrointestinal discomfort such as nausea or abdominal pain.
  • Sleep disturbances or vivid dreams.
  • Reduced exercise tolerance.
  • Mild hypoglycemia, particularly in infants.

Serious

  • Severe bradycardia or heart block.
  • Hypotension leading to fainting.
  • Bronchospasm or worsening asthma symptoms.
  • Heart failure exacerbation.
  • Severe bronchospasm requiring hospitalization.
  • Allergic skin reactions such as rash or angioedema.

Precautions & Warnings

Precautions for Hemangiol focus on patient conditions that may be aggravated by beta‑blockade and on careful monitoring during therapy.

  • Assess cardiac function before initiating therapy, especially in patients with pre‑existing bradycardia or heart block.
  • Use with caution in individuals with asthma, chronic obstructive pulmonary disease, or other reactive airway diseases.
  • Monitor blood pressure and heart rate regularly, adjusting dose if hypotension or excessive bradycardia occurs.
  • Evaluate glucose levels in infants and patients at risk of hypoglycemia, as beta‑blockers can mask symptoms.
  • Discuss potential drug interactions with other cardiovascular agents, such as calcium channel blockers or anti‑arrhythmics.
  • Consider pregnancy risk category C; weigh benefits against potential fetal exposure and consult obstetric care.

Avoid Interactions

Hemangiol can interact with several medications that influence heart rate, blood pressure, or metabolic pathways, requiring review before co‑administration.

Avoid

  • Other non‑selective beta‑blockers or high‑dose selective beta‑blockers, which may cause additive bradycardia.
  • Calcium channel blockers such as verapamil or diltiazem, increasing risk of heart block and hypotension.
  • Antidiabetic agents like insulin or sulfonylureas, because beta‑blockade can mask hypoglycemia signs.

Use with caution

  • Antihypertensive combinations (ACE inhibitors, ARBs) – monitor for excessive blood pressure lowering.
  • Anesthetic agents (e.g., epinephrine‑containing local anesthetics) – may reduce efficacy of epinephrine.
  • Antidepressants such as SSRIs or tricyclics – observe for possible QT prolongation.

Frequently Asked Questions

Hemangiol is a prescription oral solution that contains the active ingredient propranolol hydrochloride, a non‑selective beta‑adrenergic antagonist.

Hemangiol blocks beta‑adrenergic receptors, which reduces angiogenesis and slows the growth of hemangioma tissue, leading to gradual regression.

Hemangiol is primarily used in infants and young children for hemangioma, but it may also be prescribed to older children and adults for hypertension or arrhythmias.

Common side effects include fatigue, dizziness, cold hands or feet, mild gastrointestinal upset, sleep disturbances, reduced exercise tolerance, and occasional mild hypoglycemia.

If a patient experiences severe bradycardia, marked hypotension, bronchospasm, heart failure worsening, or allergic reactions such as rash or angioedema, the medication should be stopped and medical evaluation sought.

Hemangiol is classified as pregnancy category C in the EU, meaning risk cannot be ruled out; it should only be used if the potential benefit justifies the potential fetal risk.

Store the oral solution at room temperature, away from direct sunlight and moisture, and keep it out of reach of children.

Regular checks of heart rate, blood pressure, and blood glucose (especially in infants) are recommended, along with periodic assessment of cardiac function.

There are no specific food interactions, but patients should avoid excessive caffeine or other stimulants that may counteract beta‑blockade effects.

When combined with other antihypertensives, Hemangiol can cause additive blood pressure lowering; dose adjustments and close monitoring are advised.

If a dose is missed, give it as soon as remembered unless it is close to the next scheduled dose; do not double the dose.

No, Hemangiol is a prescription‑only medication and must be obtained through a licensed healthcare provider.

Published by

GNH India Pharmaceuticals Limited

Licensed pharmaceutical supplier

Last updated:

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