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Clomid (Clomiphene Citrate) 50 mg – 30 Tablets

Description

Biochem Clomid (Clomiphene Citrate) 50 mg – 30 Tablets | Oral Selective Estrogen Receptor Modulator

Biochem Clomid (Clomiphene Citrate) 50 mg – 30 Tablets is an oral pharmaceutical product. This product contains clomiphene citrate, a nonsteroidal selective estrogen receptor modulator (SERM) that influences reproductive hormone regulation through interactions with estrogen receptors.

Clomiphene citrate is widely associated with the pharmaceutical brand name Clomid. It has historically been used in reproductive medicine, particularly for the treatment of ovulatory dysfunction in selected women seeking pregnancy.

Clomiphene citrate belongs to the triphenylethylene class of compounds and has both estrogen-antagonistic and estrogen-agonistic properties, depending on the target tissue and physiological environment.

Its principal pharmacological effect involves modifying estrogen-mediated feedback within the hypothalamic-pituitary-gonadal axis.

By interfering with estrogen receptor signaling at regulatory sites, clomiphene can increase the secretion of gonadotropins, including luteinizing hormone (LH) and follicle-stimulating hormone (FSH), in appropriately selected patients.

LH and FSH are important reproductive hormones involved in ovarian follicular development, ovulation, testicular function, and sex hormone production.

Unlike aromatase inhibitors such as anastrozole (Arimidex) and exemestane (Aromasin), clomiphene does not primarily inhibit estrogen synthesis. Instead, it modifies the biological effects of estrogen through selective estrogen receptor interactions.

Clomiphene citrate consists of two geometric isomers, commonly known as enclomiphene and zuclomiphene. These isomers differ in their pharmacological characteristics and elimination behavior.

The compound has also been studied in selected male reproductive and endocrine conditions, including certain forms of secondary hypogonadism and infertility.

However, its established medical indications differ by jurisdiction, and its use in men is generally outside the traditional approved indication for ovulatory dysfunction.

Clomiphene is sometimes discussed in connection with recovery of endogenous hormone production following anabolic-androgenic steroid exposure. Such use is not an established indication, and hormonal recovery cannot be guaranteed.

Clomiphene is not an anabolic-androgenic steroid, testosterone preparation, aromatase inhibitor, or peptide hormone.

Clomid is a pharmaceutical brand name associated with clomiphene citrate. The use of this name in a Biochem product description does not independently establish pharmaceutical equivalence to a particular authorized branded preparation.

Biochem Clomid 50 mg contains 50 mg of clomiphene citrate per tablet, with 30 tablets per package. This provides 1,500 mg (1.5 grams) of total active ingredient per package.

The 50 mg strength identifies the amount of active ingredient per tablet and does not establish an appropriate individual dosage or treatment duration.

SpecificationDetails
Product NameBiochem Clomid
Alternative NamesClomid / Clomiphene Citrate / Clomifene
Active IngredientClomiphene Citrate
Associated Brand NameClomid
Tablet Strength50 mg
Package Quantity30 Tablets
Total Active Ingredient per Tablet50 mg
Total Active Ingredient per Package1,500 mg
Dosage FormOral Tablets
Drug ClassificationSelective Estrogen Receptor Modulator
Pharmacological ClassificationNonsteroidal SERM
Chemical FamilyTriphenylethylene Derivative
Molecular FormulaC₂₆H₂₈ClNO · C₆H₈O₇
Molecular WeightApproximately 598.09 g/mol
Active IsomersEnclomiphene and Zuclomiphene
Primary Molecular TargetEstrogen Receptors
Receptor ActivityTissue-Dependent Estrogen Agonist and Antagonist
Primary MechanismModulation of Estrogen-Mediated Feedback
Endocrine PathwayHypothalamic-Pituitary-Gonadal Axis
Gonadotropin EffectsCan Increase LH and FSH Secretion
Primary Clinical ApplicationSelected Ovulatory Dysfunction Conditions
Other Studied ApplicationsSelected Male Endocrine and Reproductive Conditions
Administration RouteOral
AbsorptionAbsorbed Following Oral Administration
MetabolismPredominantly Hepatic
EliminationPrimarily Through Fecal Pathways
Elimination CharacteristicsVariable; Some Isomer-Related Components Persist for Extended Periods
Aromatase InhibitionNot an Aromatase Inhibitor
Androgen Receptor ActivityNot an Anabolic-Androgenic Steroid
Prescription ClassificationPrescription Medication in Many Jurisdictions
Competitive Sports StatusProhibited Under WADA Rules
ExcipientsProduct-Specific Composition Not Confirmed
Manufacturing SpecificationsNot Independently Verified

1. Modulates Estrogen Receptor Signaling

Clomiphene citrate interacts with estrogen receptors and modifies estrogen-dependent biological signaling.

Its effects depend on tissue type, receptor distribution, and the physiological hormonal environment.

Within reproductive endocrine regulation, clomiphene can reduce the inhibitory influence of estrogen feedback at regulatory sites.

2. Influences the Hypothalamic-Pituitary-Gonadal Axis

The hypothalamic-pituitary-gonadal axis coordinates reproductive hormone production.

Clomiphene can influence this system by altering estrogen-mediated feedback, potentially increasing gonadotropin secretion.

The resulting hormonal response depends on whether the hypothalamus, pituitary gland, and reproductive organs retain sufficient functional capacity.

3. Can Increase Luteinizing Hormone Secretion

Luteinizing hormone is produced by the anterior pituitary gland and plays important roles in reproductive physiology.

In women, LH contributes to the hormonal processes associated with ovulation.

In men, LH stimulates Leydig cells in the testes, supporting endogenous testosterone synthesis.

Clomiphene may increase LH secretion in appropriately selected individuals, although the response is variable.

4. Can Increase Follicle-Stimulating Hormone Secretion

Follicle-stimulating hormone is another pituitary gonadotropin involved in reproductive function.

In women, FSH supports ovarian follicular development.

In men, FSH contributes to Sertoli cell function and regulation of spermatogenesis.

Clomiphene may increase FSH secretion by modifying estrogen-dependent endocrine feedback.

5. Has Established Applications in Ovulation Induction

Clomiphene citrate has historically been used to induce ovulation in selected women with ovulatory dysfunction.

Its therapeutic role depends on the underlying cause of infertility, reproductive hormone status, and other clinical factors.

Not every form of infertility responds to clomiphene, and successful ovulation does not guarantee pregnancy.

6. Has Been Studied in Male Endocrine Conditions

Clomiphene has been investigated in selected men with secondary hypogonadism and certain reproductive disorders.

Its effects on gonadotropin secretion may influence endogenous testosterone production when the relevant endocrine pathways remain functional.

However, clomiphene is not equivalent to testosterone replacement therapy, and clinical evidence does not support indiscriminate use for all causes of low testosterone.

7. Has Important Visual, Reproductive, and Thromboembolic Safety Considerations

Clomiphene can produce adverse effects including hot flashes, headache, nausea, abdominal discomfort, breast tenderness, mood changes, and visual disturbances.

Ovarian enlargement, ovarian hyperstimulation, and multiple pregnancy are important considerations in fertility treatment.

Rare but serious complications, including thromboembolic events and persistent visual disturbances, have been reported.

Clomiphene citrate requires appropriate medical assessment because it can affect reproductive hormones and ovarian function. Potential risks include ovarian enlargement, visual disturbances, multiple pregnancy, ovarian hyperstimulation, mood changes, and rare thromboembolic events. It should not be used during pregnancy or in individuals with certain contraindications, including active liver disease, unexplained abnormal uterine bleeding, or specified hormone-sensitive conditions. New visual symptoms warrant prompt medical evaluation.

The 50 mg tablet strength describes the quantity of clomiphene citrate in each tablet. The package contains 30 tablets, providing a total of 1,500 mg. Neither the tablet strength nor the package quantity independently establishes an appropriate dose, frequency, treatment duration, or individual medical indication.

Clomiphene citrate is an orally active selective estrogen receptor modulator whose primary reproductive endocrine effects arise from modification of estrogen-mediated feedback.

Its mechanism differs fundamentally from that of anabolic-androgenic steroids, aromatase inhibitors, and direct gonadotropin preparations.

Step 1 – Oral Administration and Gastrointestinal Absorption

Clomiphene citrate is administered orally in established pharmaceutical formulations.

Following administration, it is absorbed through the gastrointestinal tract and enters systemic circulation.

The absorption characteristics may vary according to formulation and individual physiological factors.

Step 2 – Distribution and Estrogen Receptor Interaction

After absorption, clomiphene and its isomeric components distribute to tissues expressing estrogen receptors.

The compound interacts with estrogen receptor-mediated signaling pathways.

Its pharmacological effects vary between tissues and endocrine environments.

Step 3 – Modification of Estrogen Feedback

Clomiphene can reduce estrogen-mediated negative feedback at sites involved in reproductive hormone regulation.

This may influence hypothalamic signaling and pituitary gonadotropin secretion.

The magnitude of this response depends on the individual's endocrine function and underlying medical condition.

Step 4 – Changes in LH and FSH Secretion

Altered estrogen feedback can increase pituitary secretion of LH and FSH.

These hormones influence ovarian and testicular function.

In selected women, this response can contribute to follicular development and ovulation. In selected men, it may influence endogenous testosterone production and reproductive hormone regulation.

Step 5 – Hepatic Metabolism and Elimination

Clomiphene citrate undergoes metabolic processing involving the liver.

The compound contains enclomiphene and zuclomiphene, which differ in elimination characteristics.

Some components, particularly zuclomiphene-related material, may persist for extended periods. Consequently, a single definitive half-life does not adequately describe the complete pharmacokinetic behavior of the mixture.

Elimination occurs predominantly through fecal pathways, with smaller amounts eliminated through urine.

Clomiphene citrate has historically been manufactured as oral tablets, including 50 mg pharmaceutical presentations.

The Biochem Clomid 50 mg oral tablet presentation is described by the following characteristics:

  • Clomiphene citrate as the active ingredient.
  • A tablet strength of 50 mg.
  • A package quantity of 30 tablets.
  • A total package content of 1,500 mg of clomiphene citrate.
  • Oral solid-dose pharmaceutical presentation.
  • Nonsteroidal selective estrogen receptor modulator classification.
  • Triphenylethylene-derived chemical structure.
  • Enclomiphene and zuclomiphene isomer composition.
  • Tissue-dependent estrogen receptor agonist and antagonist effects.
  • Modulation of estrogen-mediated endocrine feedback.
  • Influence on the hypothalamic-pituitary-gonadal axis.
  • Potential increases in LH and FSH secretion.
  • Established historical use in selected ovulatory dysfunction conditions.
  • Studied applications in selected male endocrine disorders.
  • No direct anabolic-androgenic steroid activity.
  • No primary aromatase inhibition.
  • Hepatic metabolism.
  • Isomer-dependent elimination characteristics.
  • Important visual and reproductive safety considerations.
  • Formulation-dependent dissolution and absorption.
  • Tablet excipients and packaging specifications requiring confirmation.
  • Product identity, purity, and content uniformity requiring analytical verification.

The precise excipient composition, tablet appearance, and manufacturing specifications of Biochem Clomid 50 mg have not been independently confirmed.

The package contains 30 tablets, but this does not establish an appropriate treatment duration or individual prescription. The product should not be represented as authentic branded Clomid or as an approved interchangeable generic without independent verification.


United States

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Canada

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United Kingdom

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Germany

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France

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Spain

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Italy

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Portugal

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Netherlands

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Belgium

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Switzerland

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Austria

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Sweden

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Norway

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Denmark

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Finland

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Poland

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Czech Republic

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Romania

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Greece

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Ireland

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Colombia

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Argentina

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México

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Perú

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Venezuela

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Ecuador

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Biochem Clomid (Clomiphene Citrate) 50mg | 30 Tablets | Selective Estrogen Receptor Modulator

Learn about Biochem Clomid 50mg, 30 tablets. This product contains clomiphene citrate, a selective estrogen receptor modulator that influences estrogen feedback, LH and FSH secretion, and reproductive hormone regulation.

Biochem Clomid (Citrato de Clomifeno) 50mg | 30 Tabletas | Modulador Selectivo de los Receptores de Estrógeno

Conoce Biochem Clomid 50mg, 30 tabletas. Este producto contiene citrato de clomifeno, un modulador selectivo de los receptores de estrógeno que influye en la regulación hormonal reproductiva y la secreción de LH y FSH.

biochem-clomid-clomiphene-citrate-50mg-30-tablets

biochem-clomid-citrato-de-clomifeno-50mg-30-tabletas

Biochem Clomid Clomiphene Citrate 50mg package containing 30 oral tablets, each containing 50mg of clomiphene citrate, a nonsteroidal selective estrogen receptor modulator associated with estrogen feedback regulation and gonadotropin secretion.

Biochem Clomid Citrato de Clomifeno 50mg presentación de 30 tabletas orales, cada una con 50mg de citrato de clomifeno, un modulador selectivo no esteroideo de los receptores de estrógeno relacionado con la regulación hormonal y la secreción de gonadotropinas.