Registered Zambia · ZAMRA

FERTAGYL

Gonadorelin 0.1 mg/ml mg/ml

ZAMRA-VM-26-103 Suspension for Injection 0.1 mg/ml mg/ml systemic hormonal preparations, excl. sex hormones and insulins INN generic

What it does

Gonadorelin is a hormone used to treat certain conditions related to hormone levels in the body.

Commonly used for: delayed puberty, infertility, hypogonadism

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Plain-language summary for general understanding - not medical advice. Always follow your pharmacist/doctor.

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Registration & product details

Registration no.
ZAMRA-VM-26-103
Registration date
2026-04-02
Expiry date
2031-04-01
Status
Registered/Compliant
Active ingredient
Gonadorelin 0.1 mg/ml mg/ml
Strength
0.1 mg/ml mg/ml
Pack size
-
Therapeutic class
-
ATC class (WHO)
H01CA - Gonadotropin-releasing hormones
RxNorm RxCUI
6384
Manufacturer / MAH
Intervet
Country of origin
The Netherlands
Manufacturer location
Wim de Körverstraat 35, 5831 AN Boxmeer, Netherlands

Source: Zambia Medicines Regulatory Authority · fetched 2026-04-14 14:03:48 · updated 2026-09-17 03:40:15

Disclaimer: This information is sourced from Zambia Medicines Regulatory Authority (Zambia). Always consult a qualified healthcare professional before using any medication.

About this medicine

Gonadorelin is a hormone used to treat certain conditions related to hormone levels in the body.

What it treats

  • delayed puberty
  • infertility
  • hypogonadism

How it works

Gonadorelin helps control the release of hormones that are important for sexual development and reproduction.

Who it's for

It is for people experiencing hormone-related issues, such as those with delayed puberty or infertility.

AI-assisted summary grounded in BNF data - general information only, not medical advice. Always confirm with your pharmacist or doctor.

Clinical monograph: Gonadorelin

BNF-referenced

Gonadorelin, also known as gonadotropin-releasing hormone (GnRH), is a synthetic analogue of the naturally occurring GnRH. It primarily stimulates the synthesis and release of luteinizing hormone (LH) and follicle-stimulating hormone (FSH) from the anterior pituitary gland. Gonadorelin plays a crucial role in regulating reproductive processes, including induction of ovulation, treatment of delayed puberty, and management of infertility due to hypogonadotropic hypogonadism.

Indications

  • Assessment of anterior pituitary function
  • Treatment of delayed puberty
  • Induction of ovulation in hypothalamic amenorrhea
  • Management of infertility caused by hypogonadotropic hypogonadism

Dosage

Adults: By intramuscular injection, initially 1 mg daily, alternatively 1 mg every 12 hours in acute cases. This can be reduced to 1 mg every 2–3 days, followed by 1 mg once weekly, or alternatively 500 micrograms every 2–3 days.

Mechanism of action

Gonadorelin stimulates the synthesis and release of LH and FSH from the anterior pituitary gland, mimicking the physiological release of GnRH from the hypothalamus. It is essential for controlling reproductive functions such as follicular growth, ovulation, and maintenance of the corpus luteum in females, as well as spermatogenesis in males. The pulsatile secretion of GnRH is necessary for effective pituitary response and reproductive function.

Pharmacodynamics

Gonadorelin is responsible for the release of LH and FSH from the anterior pituitary. Its action is influenced by the frequency and amplitude of GnRH pulses, alongside feedback from androgens and estrogens. A consistent pulsatile release is crucial for normal reproductive functionality, including ovulation in females and sperm production in males. Its pharmacological effects are significant in conditions related to reproductive health.

Pharmacokinetics

Gonadorelin has a short half-life, necessitating continuous infusion via infusion pumps for effective clinical use. The pharmacokinetic profile supports its application in conditions requiring controlled stimulation of gonadotropin release. The drug's bioavailability and tissue distribution allow it to exert localized effects on the anterior pituitary, leading to the release of key reproductive hormones.

Contra-indications

  • Acute psychosis
  • Adrenogenital syndrome
  • Active infectious diseases
  • History of hypersensitivity to tetracosactide/corticotrophins or excipients
  • Severe hypertension
  • Diabetes mellitus (without dosage adjustment)
  • Recent intestinal anastomosis
  • Psychological disturbances

Adverse effects

  • Anaphylaxis
  • Hypertension
  • Increased risk of infection
  • Leukocytosis
  • Malaise
  • Menstrual irregularities
  • Muscle weakness
  • Nausea
  • Osteonecrosis
  • Osteoporosis
  • Pancreatitis
  • Papilloedema
  • Psychiatric disorders
  • Seizures
  • Skin reactions
  • Tendon rupture
  • Thromboembolism
  • Vasculitis
  • Weight increase
  • Vomiting
  • Vertigo

Interactions

  • Antihypertensives (may require dosage adjustment)
  • Diabetes medications (may require dosage adjustment)

Precautions

  • Patients with a history of allergies, especially asthma
  • Monitor patients for signs of psychological disturbances
  • Use with caution in patients with a history of thromboembolism
  • Systemic effects may occur due to the potent nature of hormone therapy

Pregnancy

Avoid use unless essential for diagnostic purposes.

Breast-feeding

Avoid use unless essential for diagnostic purposes.

Storage

Store in a cool, dry place, away from light. Follow specific manufacturer's guidelines for storage conditions.

Formulations

  • 250 micrograms/1 ml solution for injection in ampoules
BNF 85 (British National Formulary) p.833 BNF for Children 2019-2020 p.514 PubChem / pathway

AI-synthesized from BNF references - general information only, not a substitute for professional medical advice or the current BNF. Verify doses with a pharmacist.

Molecular reference: Gonadorelin

PubChem CID 638793

Molecular formula: C55H75N17O13

Mechanism of action

Systemic - Like naturally occurring gonadotropin-releasing hormone (GnRH), gonadorelin primarily stimulates the synthesis and release of luteinizing hormone (LH) from the anterior pituitary gland. Follicle-stimulating hormone (FSH) production and release is also increased by gonadorelin, but to a lesser degree. In prepubertal females and some gonadal function disorders, the FSH response may be greater than the LH response. For the treatment of amenorrhea, delayed puberty, and infertility the administration of gonadorelin is used to simulate the physiologic release of GnRH from the hypothalamus in treatment of delayed puberty, treatment of infertility caused by hypogonadotropic hypogonadism, and induction of ovulation in those women with hypothalamic amenorrhea. This results in increased levels of pituitary gonadotropins LH and FSH, which subsequently stimulate the gonads to produce reproductive steroids.

Pharmacodynamics

Gonadorelin is responsible for the release of follicle stimulating hormone and leutinizing hormone from the anterior pitutitary. In the pituitary GnRH stimulates synthesis and release of FSH and LH, a process that is controlled by the frequency and amplitude of GnRH pulses, as well as the feedback of androgens and estrogens. The pulsatility of GnRH secretion has been seen in all vertebrates, and it is necessary to ensure a correct reproductive function. Thus a single hormone, GnRH, controls a complex process of follicular growth, ovulation, and corpus luteum maintenance in the female, and spermatogenesis in the male. Its short half life requires infusion pumps for its clinical use

Source: PubChem (NCBI) · pathways from PathBank, Reactome, WikiPathways & PharmGKB.

This drug in other countries

The same active ingredient registered across other registries we cover - including different brands.