Product image of Izifet (Levothyroxine Sodium) supplied by GNH India

Izifet

Active Ingredient:
Levothyroxine Sodium
Origin:
EU

Izifet (Levothyroxine Sodium)

Levothyroxine Sodium, the active ingredient in Izifet, is a thyroid hormone presented as an oral tablet for systemic use. It replaces deficient endogenous thyroid hormone and is used to treat hypothyroidism, thyroid hormone replacement therapy, and goiter in adults and children.

GNH India supplies Izifet as a licensed, GDP‑compliant international pharmaceutical supplier serving hospitals, pharmacies, clinics and procurement teams worldwide, ensuring quality and regulatory compliance across markets. Our distribution network adheres to stringent quality standards and supports timely delivery to healthcare providers.

Manufacturer / TM Owner

Nassington Ltd

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Indications & Clinical Uses

Levothyroxine Sodium is used to restore normal thyroid hormone levels in conditions affecting the thyroid gland.

  • Hypothyroidism: restores deficient thyroid hormone, normalizing metabolism and alleviating symptoms such as fatigue and weight gain.
  • Thyroid hormone replacement therapy after thyroidectomy or radioactive iodine: provides the necessary hormone to maintain metabolic homeostasis.
  • Goiter associated with thyroid hormone deficiency: reduces gland enlargement by correcting hormonal imbalance.

How It Works

  • Levothyroxine Sodium is a synthetic form of thyroxine (T4) that is absorbed from the gastrointestinal tract and circulates bound to plasma proteins. Within target cells, deiodinase enzymes convert it to the active triiodothyronine (T3). The resulting hormone binds nuclear thyroid hormone receptors, modulating gene transcription that regulates basal metabolic rate, protein synthesis, and growth.

Side Effects

Levothyroxine Sodium may cause a range of adverse reactions, which are grouped by frequency and severity.

Common Side Effects

  • Headache
  • Insomnia
  • Palpitations
  • Weight loss
  • Heat intolerance
  • Tremor

Serious or Rare Side Effects

  • Allergic reaction (rash, angioedema)
  • Chest pain or arrhythmia
  • Severe hyperthyroidism symptoms
  • Bone loss (osteoporosis) with long‑term overtreatment

Precautions & Warnings

When prescribing Levothyroxine Sodium, clinicians should consider several safety measures.

  • Monitor thyroid function tests regularly: adjust dose based on TSH and free T4 levels.
  • Initiate therapy with low dose in elderly patients: reduce risk of cardiac stress.
  • Avoid use in untreated adrenal insufficiency: may precipitate adrenal crisis.
  • Caution during pregnancy and breastfeeding: weigh benefits against potential fetal thyroid effects.
  • Store at ambient temperature: keep in original container, protect from moisture and light.

Avoid Interactions

Levothyroxine Sodium can interact with various medicines that affect its absorption or metabolism.

Major Interactions (Avoid)

  • Antacids containing aluminum or magnesium: decrease levothyroxine absorption.
  • Calcium supplements or calcium carbonate: bind levothyroxine and reduce bioavailability.
  • Iron salts (ferrous sulfate): impair absorption when taken concurrently.
  • Cholesterol‑lowering resins (e.g., cholestyramine): sequester levothyroxine.
  • Amiodarone: alters thyroid hormone metabolism and may require dose adjustment.

Moderate Interactions (Monitor Closely)

  • Warfarin: levothyroxine may enhance anticoagulant effect, monitor INR.
  • Corticosteroids: may increase levothyroxine clearance, watch thyroid levels.
  • Estrogen therapy (including oral contraceptives): may raise levothyroxine requirement.

Frequently Asked Questions

Izifet contains Levothyroxine Sodium, which is prescribed to replace deficient thyroid hormone in patients with hypothyroidism, to provide hormone after thyroidectomy or radioactive iodine treatment, and to treat goiter caused by hormonal imbalance.

Levothyroxine Sodium is a synthetic form of the natural hormone T4. After oral absorption it is converted to the active hormone T3 inside cells, where it binds nuclear thyroid receptors and regulates gene expression that controls metabolism, growth and development.

The appropriate dose of Izifet is individualized by the prescribing clinician based on the patient’s age, weight, severity of thyroid deficiency, and periodic laboratory measurements of TSH and free T4. No fixed regimen is provided here.

Levothyroxine Sodium is classified as a pregnancy category that requires careful risk‑benefit assessment. It is often continued in pregnancy to maintain maternal euthyroidism, which is important for fetal development. Breastfeeding mothers should discuss continuation with their healthcare provider.

To request Izifet, 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.

Izifet delivers the same active ingredient, Levothyroxine Sodium, as other branded or generic levothyroxine products. Differences may lie in manufacturing standards, excipients, and regulatory approvals. Clinical efficacy and safety are comparable when bioequivalence is demonstrated.

Store Izifet at ambient temperature, preferably below 25 °C. Keep the tablets in the original container, protect them from moisture, heat and direct light. Do not store in the bathroom or near a kitchen sink.

Izifet is taken orally, usually on an empty stomach, at least 30 minutes before breakfast. The tablet should be swallowed whole with a full glass of water. Patients should follow the dosing schedule prescribed by their healthcare professional.

Serious adverse events include signs of overt hyperthyroidism such as chest pain, arrhythmia, severe tremor, or unexplained weight loss, as well as allergic reactions like rash or swelling. Any of these symptoms require immediate medical evaluation.

Izifet should be avoided in individuals with untreated adrenal insufficiency, acute myocardial infarction, or known hypersensitivity to levothyroxine or any tablet excipients. Patients with these conditions should discuss alternative therapies with their physician.

Published by

GNH India Pharmaceuticals Limited

Licensed pharmaceutical supplier

Last updated:

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