Product image of Kessar (Tamoxifen Citrate) supplied by GNH India

Kessar

Active Ingredient:
Tamoxifen Citrate
Origin:
EU

Kessar (Tamoxifen Citrate)

Tamoxifen citrate, the active ingredient in Kessar, is a selective estrogen receptor modulator presented as an oral tablet for oral use. It is employed in hormone therapy to treat estrogen receptor‑positive breast cancer and to reduce cancer risk in women at high risk.
GNH India supplies Kessar as a licensed, GDP‑compliant international pharmaceutical supplier serving hospitals, oncology centres, pharmacies and clinics worldwide.

Manufacturer / TM Owner

Orion Corporation

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Indications & Clinical Uses

Tamoxifen citrate is a SERM used in the management of estrogen‑driven breast cancer and related risk scenarios.

  • Adjuvant breast cancer: improves disease‑free survival after surgery in estrogen receptor‑positive patients.
  • Metastatic breast cancer: slows disease progression in advanced hormone‑sensitive tumors.
  • High‑risk women: lowers the incidence of invasive breast cancer in women with a strong family or genetic predisposition.

How It Works

  • Tamoxifen citrate binds competitively to estrogen receptors in breast tissue, blocking estrogen‑mediated cellular proliferation. In bone and uterine tissue it exhibits partial agonist activity, preserving bone density while exerting a mixed effect on the uterus. This selective modulation disrupts the growth signal cascade in estrogen‑dependent tumors, leading to cell cycle arrest and apoptosis.

Side Effects

Tamoxifen citrate may cause a range of adverse reactions that vary in frequency and severity.

Common Side Effects

  • Hot flashes: transient episodes of warmth and sweating.
  • Nausea: mild to moderate stomach upset.
  • Fatigue: persistent tiredness not relieved by rest.
  • Vaginal discharge or dryness: changes in genital secretions.
  • Menstrual irregularities: altered cycle length or flow.
  • Weight gain: modest increase in body weight.

Serious or Rare Side Effects

  • Deep vein thrombosis or pulmonary embolism: signs of clot formation.
  • Endometrial cancer: abnormal uterine bleeding.
  • Liver toxicity: jaundice or elevated liver enzymes.
  • Visual disturbances: blurred vision or retinal changes.
  • Severe allergic reaction: rash, swelling, or breathing difficulty.

Precautions & Warnings

Before initiating tamoxifen citrate therapy, consider the following safety measures.

  • Pregnancy testing: confirm non‑pregnant status before starting treatment.
  • Thromboembolic risk: assess personal or family history of clotting disorders.
  • Liver function: obtain baseline liver enzyme tests and monitor periodically.
  • Ocular health: schedule regular eye examinations for patients with visual symptoms.
  • Drug interactions: review concomitant medications for potential CYP2D6 inhibitors.
  • Store at ambient temperature: keep below 25 °C in the original container, protect from moisture and direct sunlight.

Avoid Interactions

Tamoxifen citrate can interact with several medicines, altering its effectiveness or safety profile.

Major Interactions (Avoid)

  • Strong CYP2D6 inhibitors (e.g., paroxetine, fluoxetine): may reduce tamoxifen activation.
  • Anticoagulants (e.g., warfarin): increased risk of bleeding.
  • Hormonal contraceptives: may diminish contraceptive efficacy.

Moderate Interactions (Monitor Closely)

  • SSRIs with weak CYP2D6 inhibition (e.g., sertraline): monitor therapeutic response.
  • Aromatase inhibitors: overlapping endocrine effects require clinical judgment.
  • Herbal supplements (e.g., St. John’s wort): may induce metabolism and lower drug levels.

Frequently Asked Questions

Kessar contains tamoxifen citrate, a selective estrogen receptor modulator used primarily as hormone therapy for estrogen receptor‑positive breast cancer, both in the adjuvant setting after surgery and for metastatic disease, as well as for reducing breast cancer risk in women who are at high genetic or familial risk.

Tamoxifen citrate binds to estrogen receptors in breast tissue, acting as a competitive antagonist that blocks estrogen‑driven cell proliferation. In other tissues such as bone, it behaves as a partial agonist, helping maintain bone density while still inhibiting tumor growth.

The dosage of Kessar is individualized by the prescribing clinician based on the patient’s condition, treatment stage, and overall health. Healthcare professionals determine the appropriate strength, frequency, and duration of therapy.

Tamoxifen citrate is contraindicated in pregnancy because it can cause fetal harm. Women of child‑bearing potential should use effective contraception during treatment and for a period after discontinuation. Breastfeeding is not recommended while taking tamoxifen.

To request Kessar, 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.

Kessar (tamoxifen) is a SERM, differing from aromatase inhibitors which lower systemic estrogen levels. Tamoxifen is often chosen for pre‑menopausal patients or when a partial estrogen agonist effect is desired, whereas aromatase inhibitors are typically used in post‑menopausal women.

Store Kessar at ambient temperature, preferably below 25 °C. Keep the tablets in the original blister pack, protect them from moisture and direct sunlight, and ensure the container is tightly closed to maintain product stability.

Kessar is taken orally, usually with water. The tablet should be swallowed whole and not chewed or crushed, unless the prescriber provides specific instructions for a different administration method.

Serious risks include thromboembolic events such as deep‑vein thrombosis or pulmonary embolism, endometrial cancer indicated by abnormal uterine bleeding, and severe liver toxicity. Patients should be monitored for signs of these conditions and report any concerning symptoms promptly.

Kessar should be avoided in patients with a known hypersensitivity to tamoxifen or any of its excipients, in pregnant women, and in individuals with a history of thromboembolic disorders or uncontrolled liver disease unless the benefits outweigh the risks as judged by a qualified clinician.

Published by

GNH India Pharmaceuticals Limited

Licensed pharmaceutical supplier

Last updated:

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