Drug Guide
Ganirelix Acetate
Classification
Therapeutic: Gonadotropin-releasing hormone (GnRH) antagonist
Pharmacological: Peptide hormone
FDA Approved Indications
- Controlled ovarian stimulation in assisted reproductive technology (ART) procedures to prevent premature ovulation
Mechanism of Action
Ganirelix competitively binds to GnRH receptors in the pituitary gland, thereby inhibiting the secretion of luteinizing hormone (LH) and follicle-stimulating hormone (FSH), preventing premature ovulation during ART.
Dosage and Administration
Adult: Typically, 0.25 mg subcutaneously once daily, starting on day 5 of ovarian stimulation, until the day of hCG administration.
Pediatric: Not approved for pediatric use.
Geriatric: Use with caution; no specific dosage adjustments are established.
Renal Impairment: Use with caution; no specific dosage adjustments established.
Hepatic Impairment: Use with caution; no specific dosage adjustments established.
Pharmacokinetics
Absorption: Rapid, subcutaneous absorption.
Distribution: Widely distributed with a volume of distribution approximately 27-38 L.
Metabolism: Metabolized by plasma peptidases.
Excretion: Primarily excreted as peptides in urine.
Half Life: Approximately 16-18 hours.
Contraindications
- Hypersensitivity to ganirelix or any component of the formulation.
Precautions
- Use during pregnancy unless clearly needed; monitor for severe allergic reactions; caution in patients with known hypersensitivity to similar peptides.
Adverse Reactions - Common
- Injection site reactions (pain, redness, swelling) (Common)
- Headache (Common)
- Nausea (Common)
Adverse Reactions - Serious
- Severe allergic reactions including anaphylaxis (Rare)
- Ovarian hyperstimulation syndrome (Rare)
Drug-Drug Interactions
- No significant interactions documented.
Drug-Food Interactions
- None established.
Drug-Herb Interactions
- None established.
Nursing Implications
Assessment: Monitor ovarian response and serum LH, FSH levels as indicated.
Diagnoses:
- Risk for ovarian hyperstimulation syndrome
- Anxiety related to fertility treatments
Implementation: Administer subcutaneously as prescribed; observe for allergic reactions.
Evaluation: Assess ovarian response and confirm the prevention of premature ovulation.
Patient/Family Teaching
- Instruct patient on proper injection technique.
- Inform about possible side effects and when to seek medical attention.
- Explain the importance of adherence to medication schedule.
Special Considerations
Black Box Warnings:
- None specifically related to ganirelix, but caution should be observed in patients with hypersensitivity.
Genetic Factors: No known genetic considerations.
Lab Test Interference: May alter hormone levels used in monitoring ovarian stimulation.
Overdose Management
Signs/Symptoms: Uncommon; overdose may increase risk of adverse reactions such as ovarian hyperstimulation syndrome.
Treatment: Supportive care; symptomatic management; no specific antidote.
Storage and Handling
Storage: Store refrigerated at 2°C to 8°C (36°F to 46°F). Keep in original container to protect from light.
Stability: Stable until the expiration date when stored properly.