Cyclogest

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Medically reviewed

Marina Burgos

Last updated on 22/12/2025

This page provides general, reference-level information compiled from official medical sources. It is not a substitute for professional medical advice, diagnosis, or treatment. For decisions about your health, please consult a qualified healthcare professional.

Overview of Cyclogest

What is Cyclogest? Defining the Progesterone Drug

The following quick facts define the core identity of this pharmaceutical preparation.

Property Description
Active ingredient Progesterone (Micronized)
Form Pessary or Suppository
Pharmacological class Progestogen (Steroid Hormone)
General purpose Hormone supplementation
Origin Natural-occurring (Bioidentical)

What is Cyclogest and What Type of Drug is it?

Cyclogest is a prescription-only medicine (POM) whose sole active ingredient is Progesterone, a hormone used to supplement or replace the body's natural levels. It is classified as a progestogen, also known as a Gestagen, belonging to the essential steroid hormones pharmacological class. This classification defines the drug's role in the body as a regulator of specific reproductive functions.

The brand name Cyclogest specifically distinguishes this product's formulation and delivery method. The formulation is clinically recognized for delivering micronized Progesterone, which is structurally and chemically identical (bioidentical) to the hormone produced by the female body.


Composition, Origin, and Form of Cyclogest

The drug is a single-ingredient product featuring natural micronized progesterone formulated into a pessary or suppository, utilizing a hard fat base. This formulation is distinctive because it offers flexibility in its route of administration, allowing either vaginal or rectal insertion, which is a key consideration for patients with specific needs or tolerances.


Cyclogest's General Purpose and High-Level Function

The general purpose of Cyclogest is hormone supplementation, achieved by raising the body's Progesterone levels to support conditions dependent on adequate hormonal presence. The key physiological action is to promote the proper preparation of the endometrium, the uterine lining, and induce uterine relaxation. Progesterone serves to ensure the continuation of specific phases of the reproductive cycle. The medication's core function is to maintain a stable, supported state in the uterus.

What side effects are possible with Cyclogest?

Possible side effects and safety information

The safety profile of Cyclogest is based on regulatory classifications that organize adverse reactions by frequency and the affected body system. This ensures a medically precise description of potential effects without providing clinical advice or interpretation.


Frequency and System-Organ Classifications

The following frequency classifications for adverse reactions are documented in official regulatory labeling:

Classification Examples of Adverse Reactions Affected System-Organ Class
Common (up to 1 in 10 users) Drowsiness, Headache, Nausea, Abdominal pain, Fatigue Nervous System, Gastrointestinal, General Disorders
Uncommon (up to 1 in 100 users) Spotting, Local irritation, Breakthrough bleeding, Hot flushes Reproductive System, Administration Site Conditions

Drowsiness is a specifically noted side effect, which is officially stated to be more likely when the medicine is administered via the rectal route.


Safety Restrictions and Contraindications

Official prescribing information defines specific safety limitations. The medicine is contraindicated and should not be used in individuals with a current or history of thromboembolic disorders (such as deep vein thrombosis or pulmonary embolism), severe hepatic dysfunction, or undiagnosed vaginal bleeding. Furthermore, its use is prohibited in patients with known or suspected hormone-dependent malignant tumors or porphyria. These restrictions are based on formal safety assessments documented in regulatory sources.

Overdose and Emergency Response

Overdose and when to seek help

The following information is based strictly on the officially documented overdose and emergency response instructions found in governmental regulatory sources for Cyclogest (Progesterone).

Documented Overdose Manifestations

Official prescribing information for Cyclogest states that the medication possesses a wide margin of safety, and an overdose is generally not expected to be dangerous.

Overdosage may potentially lead to the documented clinical signs of euphoria (mental changes) or dysmenorrhoea (painful menstruation).

Official Emergency Actions

Regulators mandate that individuals seek immediate medical attention or urgent medical attention in cases of accidental swallowing of the pessaries or use of too many.

This action requires contacting a doctor, the Emergency Department, or a Poison Control Center immediately. Help must be sought even if there are no signs of discomfort or poisoning, as mandated by official instructions for exposure or overuse.

Population-Specific Data Constraints

Regulatory documents note that the official overdose profile is constrained by a lack of specific clinical data in certain groups. There is no experience with use in patients with impaired liver or renal function, and no clinical data have been collected in patients over age 65.

Therapeutic Uses of Cyclogest

What Cyclogest Treats: Main Uses and Benefits

Cyclogest is generally used across therapeutic domains where supportive symptom management is appropriate, often applied during phases when symptoms become more noticeable or intensify. Clinical indications include the management of symptoms linked to premenstrual syndrome (PMS), puerperal (post-natal) depression, and providing luteal phase support in Assisted Reproductive Technology (ART).

It is applicable in conditions characterized by periods of heightened symptoms that lead to functional strain. This includes scenarios where symptoms relate to systemic imbalance or fluctuate suddenly. The medication supports the patient during difficult episodes by easing discomfort and helps maintain a sense of stability when symptoms are more noticeable.

“Applied in contexts where additional symptomatic support is needed, this medicine contributes to improved patient comfort during symptomatic periods.”


Quick Facts

  • Support for Symptoms that Interfere with Daily Functioning
  • Relevant for easing symptoms linked to systemic imbalance
  • Assists with maintaining functional stability when symptoms become momentarily overwhelming

Eligibility and Restrictions for Use

Who can and cannot use Cyclogest?

The eligibility for Cyclogest (progesterone pessary) is strictly defined by regulatory authorities, outlining specific populations who may use the medicine and those who must not.

Absolute Contraindications (Must Not Use) The medicine is strictly contraindicated for individuals with:

  • Severe hepatic (liver) disease.
  • Active arterial or venous thromboembolism or a history of these events.
  • Known or suspected hormone-sensitive cancers, such as breast or uterine malignancy.
  • Undiagnosed vaginal bleeding or specific conditions like Porphyria disorders.
  • Diagnosed complications such as known missed abortion or ectopic pregnancy.

Conditional Use and Restrictions Use is generally established for adult women requiring luteal phase support in the first trimester of pregnancy as part of an Assisted Reproductive Technology (ART) program.

Eligibility Status Specific Population Limitation
Conditional Use Patients with diabetes, a history of depression, or pre-existing conditions like cardiac/renal dysfunction require careful medical observation.
Age/Lactation The medicine is not intended for the paediatric population or women over 65 years of age and is not recommended while breastfeeding.

What should I know about interactions with other medicines?

Interactions with other medicines and products

Official regulatory documents detail specific constraints regarding the concomitant use of other medicines, herbal products, and local products due to potential changes in the effectiveness of progesterone or mechanical interference with the drug product.

Systemic Drug-Drug Interactions

Interactions that may alter the effectiveness of this medicine are primarily related to changes in liver enzyme activity. This may necessitate monitoring by a healthcare professional.

Interaction Type Interacting Medicines Explicitly Listed
Decreased Effectiveness Carbamazepine, Phenytoin, Rifampicin (Enzyme Inducers)
Increased Effectiveness Ketoconazole (Enzyme Inhibitor)
  • Medicines such as Carbamazepine, Phenytoin, and Rifampicin can potentially reduce the effectiveness of Cyclogest.
  • The antifungal medicine Ketoconazole may potentially increase the effectiveness of Cyclogest.

Local and Procedural Interaction Constraints

The formulation of this medicine imposes specific local restrictions on co-administration with other products:

  • Avoidance of local products: The use of other vaginal products should be avoided during the use of this medicine.
  • Barrier Contraceptives: The hard fat components within the pessary may compromise the material integrity of barrier methods of birth control, such as diaphragms, cervical caps, or condoms, potentially making them unreliable for preventing pregnancy.

Mechanism of Action

The mechanism of Progesterone (Cyclogest) involves three core biological domains, acting primarily as a hormone agonist to regulate specific physiological pathways.


Modulating Uterine Tissue and Muscle Quiescence

Progesterone acts as a highly specific agonist for its Nuclear Receptors (PRs) in the uterus, initiating a genomic cascade that modulates gene expression. This action promotes the transformation of the uterine lining into a secretory structure (decidualization). Additionally, its action suppresses the muscle layer's electrical excitability and contraction proteins, leading to myometrial quiescence (uterine relaxation).


Neurosteroid Activity and Central Signaling

Progesterone is metabolized into active neurosteroids, such as Allopregnanolone, which function as a positive allosteric modulator of the inhibitory GABA A receptor in the brain. By enhancing GABAergic signaling, this mechanism contributes to the hyperpolarization and neuronal stabilization in the central nervous system.


Regulation of Fluid and Electrolyte Balance

The molecule also exhibits weak antagonism at the Mineralocorticoid Receptor (MR) in the kidney. By competitively blocking this receptor, the drug inhibits the reabsorption of sodium and water in the renal tubules. This physiological effect influences fluid and electrolyte homeostasis, leading to increased excretion of sodium and water.

Dosage and Administration Information

How to use Cyclogest: Official Administration Guidelines

Cyclogest (micronised progesterone) is administered via vaginal or rectal insertion, never by mouth. The specific dose, frequency, and duration are determined by the medical indication and must be followed as prescribed by a healthcare professional.

Official Dosing and Administration

Indication Dosing Schedule Route of Administration
Luteal Phase Support (ART) 400 mg twice a day (morning and evening) Vaginal
Premenstrual Syndrome / Puerperal Depression 200 mg daily up to 400 mg twice a day Vaginal or Rectal

For Luteal Phase Support (ART), treatment begins on the day of oocyte retrieval. If pregnancy is confirmed, administration should continue for 38 days from the start of therapy. For Premenstrual Syndrome, treatment should start on day 14 of the menstrual cycle and continue until the onset of menstruation.

Procedural Steps and Special Conditions

Always wash your hands thoroughly before and after inserting the pessary. The pessary is inserted deeply into either the vagina or the rectum.

  • Use the rectal route if a vaginal infection (e.g., moniliasis), recurrent cystitis, recent childbirth, or the use of a barrier contraceptive is present.
  • Use the vaginal route if the patient suffers from colitis or faecal incontinence.

If a dose is missed, insert it as soon as remembered, unless the next dose is almost due. Do not use a double dose to compensate for the missed one. There are no specific established recommendations for use in the paediatric population or patients over 65.

Recent Clinical Evidence

Research Evidence / Overview of Studies for Cyclogest

This overview summarizes the types of clinical research conducted for Cyclogest, focusing on what studies explored, the patterns observed in the evidence, and where uncertainties remain.


Evidence for Use in Assisted Reproductive Technology (ART) and Fertility Support

The use of Cyclogest was evaluated for Luteal Phase Support (LPS) during fertility treatments, such as In Vitro Fertilization (IVF). Research here primarily consists of Randomized Controlled Trials (RCTs) and meta-analyses. These studies focused on women undergoing controlled ovarian stimulation to measure outcomes relevant to the studied outcomes of conception and pregnancy progression. The overall body of evidence described patterns in measured outcomes when progesterone was compared to no treatment.

Evidence for Symptom Management: Premenstrual Syndrome (PMS)

Cyclogest was studied for the management of symptoms associated with Premenstrual Syndrome (PMS) or Premenstrual Tension. Research focused on Randomized, Double-Blind, Placebo-Controlled Trials (RCTs). Studies examined patient-reported experiences and measured outcomes related to physical discomfort and daily functioning using standardized symptom scales. Findings related to the study's primary outcome measurements have been mixed or inconsistent across the available high-quality trials.


Evidence in Other Contexts: Threatened Miscarriage and Puerperal Depression

For threatened miscarriage, research includes both RCTs and comparative studies focusing on pregnant women presenting with first-trimester bleeding. Outcomes related to the continuation of pregnancy and live birth rates were monitored. A number of studies described measured outcomes that were observed in women with a history of recurrent miscarriage. For puerperal depression, the evidence base is considerably more limited, mainly comprising older, non-randomized studies. Data for the therapeutic use of natural progesterone in this context remain insufficient for widespread conclusions.

What is Still Uncertain About Cyclogest's Research Base

One consistent research limitation is that evidence quality varies across studies. Data for certain groups, such as those with specific comorbid conditions, remain insufficient. In most clinical trials, the follow-up durations were limited, particularly for fertility support, where monitoring typically stops around the end of the first trimester of pregnancy.

Key Studies & References

  1. The efficacy and safety of luteal phase support with progesterone following ovarian stimulation and intrauterine insemination: A systematic review and meta-analysis
  2. Efficacy of progesterone and progestogens in management of premenstrual syndrome: systematic review

Frequently Asked Questions (FAQ)

Common questions about Cyclogest (FAQ)


Q: What are the approved medical uses for Cyclogest in different countries?

A: Official prescribing documents across various regions commonly list its approved uses as Luteal Phase Support as part of Assisted Reproductive Technology (ART) treatment, Premenstrual Syndrome, and Puerperal Depression. The specific indications for which the medicine is approved can vary slightly depending on the country’s regulatory authority.

Q: Is Cyclogest the same type of progesterone as other vaginal/rectal suppositories?

A: Cyclogest contains micronized progesterone, which is structurally and chemically identical (bioidentical) to the hormone produced by the body. While other vaginal or rectal progesterone products may also contain this specific active ingredient, the formulation and strength can differ between brands.

Q: Can Cyclogest affect the results of other medical tests?

A: Regulatory warnings state that the presence of progesterone may influence the results of certain laboratory tests, including those for endocrine function (hormone levels) and liver function. Official documents state that healthcare providers should be informed of its use before any such testing is conducted.

Q: Is it normal to have a significant increase in vaginal discharge when using the pessary?

A: Official product information notes that discharge or leakage of the non-active excipient material is a commonly expected observation. This occurs because the hard fat base used to form the pessary melts inside the body, and some residue may pass out of the vagina.

Q: Does the vaginal leakage mean the medication was not fully absorbed?

A: Some leakage of the hard fat base is an expected occurrence and does not necessarily indicate a lack of absorption. Clinical studies focusing on the product's effectiveness indicate that the dose provides the necessary support for the studied therapeutic effects, despite some leakage being noted.

Q: Is Cyclogest safe to use during the later stages of pregnancy?

A: Official prescribing information establishes its use for Luteal Phase Support during the first trimester of pregnancy (typically up to 38 days of treatment). Its use in later stages of pregnancy is not generally defined within the current regulatory indication for this product.

Q: How is Cyclogest absorption different when administered vaginally versus rectally?

A: Pharmacokinetic studies—which look at how the drug moves through the body—indicate that both administration routes lead to systemic absorption of the hormone. However, the rectal route may lead to a higher peak concentration in the bloodstream over a shorter period compared to vaginal administration.

Q: Is Cyclogest designed to induce or delay a menstrual period?

A: For Premenstrual Syndrome treatment, the administration schedule is specified to continue until the onset of menstruation. Reports filed on adverse reactions note that menstruation may occur earlier than expected or, more rarely, may be delayed.

Q: Can the pessary be swallowed by mistake?

A: The medicine is formulated only for vaginal or rectal insertion and must not be swallowed. Official instructions state that immediate medical attention should be sought if the pessary is accidentally ingested.

Q: Are there any dietary restrictions or lifestyle changes advised while taking Cyclogest?

A: Official regulatory documents generally contain no specific dietary restrictions for this medicine. However, patients are typically advised to inform their doctor if they consume alcohol, as this is sometimes noted as a factor to discuss with a healthcare provider.

Q: Can Cyclogest cause mood changes, such as increased anxiety or depression?

A: Official documentation lists change in mood as a possible, less serious side effect. It is also noted that worsening of depression is a potential serious effect. Official documents note that patients with a history of depression are generally subjects of careful medical observation during use.

Q: How does the concentration (200mg vs 400mg) relate to the different uses of the medicine?

A: Official prescribing information specifies the dose needed for each condition. The 400 mg dose is indicated for Luteal Phase Support in ART, while both the 200 mg and 400 mg dose forms are utilized for conditions such as Premenstrual Syndrome and Puerperal Depression.

Q: What is the purpose of the 'hard fat' ingredient in the pessary?

A: The hard fat is a non-active ingredient (excipient) used to form the pessary into its suppository shape. Its primary purpose is to serve as a base that will melt safely at body temperature to release the active progesterone for absorption.

Q: Why is Cyclogest not generally recommended for use during breastfeeding?

A: The regulatory assessment notes that a small amount of progesterone is excreted in breast milk. Due to this potential transfer, official regulatory documents state that the medicine is not generally recommended for use during breastfeeding.

Q: What are the general research findings on using Cyclogest for post-natal depression?

A: Studies and official information indicate that the research evidence for the therapeutic use of natural progesterone in the context of post-natal depression is generally described as being limited or insufficient for making widespread conclusions.

Q: What is the recommended position to be in after inserting the pessary for best absorption?

A: Official product leaflets sometimes suggest the user may find it easier to insert the pessary while lying down or squatting. Patients are sometimes noted in official materials as benefiting from remaining in a comfortable position for a short time afterward to allow the pessary to melt and be absorbed.

Q: Does Cyclogest affect blood pressure or cardiovascular health?

A: Official warnings note that patients with pre-existing conditions like cardiac or renal dysfunction require careful medical observation during use. Additionally, the drug is contraindicated (should not be used) in individuals with a current or history of thromboembolic disorders (blood clots).

Q: Are there specific patient populations that require extra caution when using Cyclogest?

A: Official prescribing information notes that patients with pre-existing conditions such as diabetes, asthma, epilepsy, migraine, or a history of depression require careful medical observation. These conditions necessitate monitoring due to potential hormonal effects.

Q: What are the known effects of taking a higher-than-usual amount of progesterone?

A: Official regulatory documents state that overdosage may produce central nervous system effects such as euphoria or adverse effects like dysmenorrhoea (painful periods). Sedation is also widely reported as the main side effect from high doses.

Q: Is it normal to experience dizziness or drowsiness after using Cyclogest?

A: Drowsiness is classified in official documents as a Common side effect, reported in up to 1 in 10 users. It is also noted that this effect is more likely when the medicine is administered via the rectal route.

Q: Can Cyclogest cause constipation, and is the route of administration related to this?

A: Official side effect reports list constipation and abdominal pain as Common adverse reactions. While less common, the rectal route of administration has been specifically linked to reports of diarrhea and flatulence.

Q: Is a severe headache a potential side effect that requires immediate medical attention?

A: While a standard headache is listed as a Common side effect, official patient information cautions that a severe headache or vomiting can be a sign of a serious event (such as a blood clot). Official patient information notes that immediate medical attention should be sought for these severe symptoms.

Q: Can Cyclogest affect the reliability of barrier contraception methods like condoms?

A: Official warnings note that the hard fat base of the pessary may compromise the material integrity of barrier methods of birth control (such as condoms, diaphragms, or cervical caps). This may potentially make them unreliable for preventing pregnancy.

Q: Can taking Cyclogest change the timing or flow of a menstrual period?

A: Reports indicate that changes to the menstrual cycle can occur as an adverse reaction. Official documentation notes that menstruation may occur earlier than expected or, more rarely, may be delayed while using this medicine.

Q: What happens in the body when Cyclogest treatment is stopped suddenly?

A: Official patient information notes that stopping the medicine suddenly may cause effects such as increased anxiety, moodiness, and an increased chance of seizures. Official guidance states that a healthcare provider should be consulted before discontinuing use.

Q: Why are the pessaries sometimes inserted rectally instead of vaginally?

A: The dual administration route offers flexibility for patients who have vaginal conditions (e.g., infection, recent childbirth, or are using a barrier contraceptive) that would make the vaginal route impractical or interfere with the medicine’s delivery.

How should Cyclogest be stored and disposed of?

Storage and Disposal Requirements for Cyclogest

The official storage profile for Cyclogest is defined by specific environmental and safety constraints to maintain product stability. The medicine must be stored in a dry place at a temperature not above 30°C and should be protected from heat and direct sunlight. Regulatory documents require keeping Cyclogest out of the sight and reach of children.

Handling and Disposal

The product's documented shelf-life is 4 years when stored under the required conditions. It must not be used after the expiry date. For disposal, expired or unused Cyclogest should not be discarded via household waste or wastewater. Instead, it must be returned to a pharmacy for safe disposal according to pharmaceutical waste handling regulations, which helps protect the environment.

Attention! Always consult to a doctor or pharmacist before using pills or medicines.

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Equivalent of Cyclogest found in:

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