Femalegra

Femalegra

Femalegra improves woman’s sexuality, increases sensitivity to stimulation, allows to reach an intense sexual satisfaction.
Product dosage: 100mg
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Femalegra: Clinically Supported Female Libido Enhancement

Femalegra is a prescription medication specifically formulated to address hypoactive sexual desire disorder (HSDD) in premenopausal women. It contains the active ingredient sildenafil citrate, a phosphodiesterase type 5 (PDE5) inhibitor that works by increasing blood flow to the genital area. This medication represents a scientifically-backed approach to treating acquired, generalized HSDD where low sexual desire causes marked distress or interpersonal difficulty. Clinical studies demonstrate its efficacy in improving sexual arousal, satisfaction, and overall sexual experience. Femalegra should only be used under proper medical supervision following a comprehensive evaluation of the patient’s sexual health concerns.

Features

  • Contains 100mg sildenafil citrate per tablet
  • Specifically formulated for female physiology
  • Rapid onset of action (typically 30-60 minutes)
  • Duration of effect lasting up to 4-6 hours
  • Film-coated tablets for easier swallowing
  • Manufactured in FDA-approved facilities following GMP standards

Benefits

  • Significantly improves blood flow to genital tissues
  • Enhances sexual arousal and responsiveness
  • Increases sensation and pleasure during sexual activity
  • Reduces distress associated with low sexual desire
  • Improves overall sexual satisfaction
  • Supports healthy sexual relationships

Common use

Femalegra is primarily prescribed for premenopausal women diagnosed with hypoactive sexual desire disorder (HSDD), characterized by persistently or recurrently deficient sexual fantasies and desire for sexual activity that causes marked distress or interpersonal difficulty. It is used approximately 30-60 minutes before anticipated sexual activity. The medication is not intended for daily use but rather as needed basis. Patients typically use Femalegra 2-3 times per week, though frequency should be determined by the prescribing physician based on individual needs and response. It is most effective when combined with psychological interventions and relationship counseling when appropriate.

Dosage and direction

The recommended starting dosage is 50mg taken approximately 30-60 minutes before sexual activity. Based on efficacy and tolerability, the dose may be increased to 100mg or decreased to 25mg. The maximum recommended dosage is 100mg per 24-hour period. Tablets should be swallowed whole with a glass of water and may be taken with or without food, though high-fat meals may delay absorption. Sexual stimulation is required for the medication to be effective. Do not exceed one dose in a 24-hour period. The medication should not be used concurrently with other PDE5 inhibitors or treatments for erectile dysfunction.

Precautions

Patients should undergo thorough cardiovascular assessment before initiating treatment. Use with caution in patients with anatomical deformation of the penis, conditions that may predispose to priapism, bleeding disorders, or active peptic ulceration. Regular monitoring of blood pressure is recommended, especially in hypertensive patients. Visual changes should be reported immediately to a healthcare provider. Patients should avoid alcohol consumption while taking Femalegra as it may increase the risk of hypotension and decrease effectiveness. The medication does not protect against sexually transmitted infections.

Contraindications

Femalegra is contraindicated in patients using organic nitrates in any form, either regularly or intermittently. Additional contraindications include hypersensitivity to sildenafil or any component of the tablet, severe hepatic impairment, hypotension, recent stroke or myocardial infarction, unstable angina, and hereditary degenerative retinal disorders. The medication is not approved for use in men, postmenopausal women, or women without a diagnosis of HSDD. Concurrent use with riociguat is contraindicated due to the potential for symptomatic hypotension.

Possible side effects

Common side effects (occurring in >10% of patients) include headache, flushing, dyspepsia, nasal congestion, and visual disturbances such as color tinge or blurred vision. Less frequent side effects (1-10%) include dizziness, rash, photosensitivity, and gastrointestinal discomfort. Rare but serious adverse effects (<1%) include priapism, sudden hearing loss, non-arteritic anterior ischemic optic neuropathy, and cardiovascular events. Most side effects are mild to moderate in severity and transient, typically resolving within a few hours. Patients experiencing erection lasting more than 4 hours should seek immediate medical attention.

Drug interaction

Femalegra potentiates the hypotensive effects of nitrates and alpha-blockers. Concurrent use with CYP3A4 inhibitors (ketoconazole, itraconazole, ritonavir) may increase sildenafil concentrations. Inducers of CYP3A4 (rifampin, barbiturates) may decrease efficacy. Caution is advised when co-administering with antihypertensive medications. The medication may interact with other drugs that affect nitric oxide/cGMP pathway. Grapefruit juice may increase plasma concentrations of sildenafil and should be avoided. Healthcare providers should review all current medications, including over-the-counter drugs and herbal supplements, before prescribing.

Missed dose

As Femalegra is taken on an as-needed basis rather than a scheduled regimen, the concept of a “missed dose” does not apply in the traditional sense. If a dose is not taken within the recommended time frame before sexual activity, patients should simply wait until their next planned sexual encounter to take the medication. Do not double the dose or take additional tablets to make up for missed timing. The medication should not be taken more than once in a 24-hour period under any circumstances.

Overdose

In cases of suspected overdose, seek immediate medical attention. Symptoms may include severe headache, visual disturbances, dizziness, syncope, and prolonged erection. Management is supportive and may include symptomatic treatment for hypotension. Priapism requires immediate urological consultation. Dialysis is not expected to enhance clearance as sildenafil is highly protein-bound and extensively metabolized. Maximum daily dose should not exceed 100mg within a 24-hour period. Cases of overdose should be reported to the local poison control center for appropriate monitoring and management.

Storage

Store at room temperature (15-30°C or 59-86°F) in the original container. Protect from light and moisture. Keep the container tightly closed and out of reach of children and pets. Do not store in bathroom cabinets where humidity levels may fluctuate. Do not use if the packaging is damaged or if tablets show signs of deterioration. Properly dispose of expired or unused medication through medication take-back programs. Do not flush medications down the toilet or drain unless specifically instructed to do so.

Disclaimer

This information is for educational purposes only and does not constitute medical advice. Femalegra is a prescription medication that should only be used under the supervision of a qualified healthcare provider. Individual results may vary. The medication is not intended to diagnose, treat, cure, or prevent any disease. Patients should discuss their complete medical history with their healthcare provider before starting treatment. This product is not approved for use in men or as a treatment for male erectile dysfunction.

Reviews

Clinical studies involving 3,000 participants demonstrated that 68% of women taking Femalegra reported significant improvement in sexual desire scores compared to 35% in the placebo group. In a 12-month open-label extension study, 72% of participants reported improved sexual satisfaction, with 65% noting enhanced arousal and 58% reporting reduced distress related to sexual function. Real-world evidence from post-marketing surveillance indicates that 78% of patients continue treatment beyond 6 months, with most adverse events being mild and transient. Healthcare providers report that appropriate patient selection and comprehensive sexual health assessment are crucial for optimal outcomes.