Lovegra: Clinically Formulated for Female Sexual Arousal
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Lovegra is a prescription medication specifically developed to address female sexual dysfunction, particularly hypoactive sexual desire disorder (HSDD) and female sexual arousal disorder (FSAD). It contains sildenafil citrate, a phosphodiesterase type 5 (PDE5) inhibitor, which works by increasing blood flow to the genital area, thereby enhancing physiological arousal and sensitivity. This medication is intended for use under medical supervision as part of a comprehensive approach to sexual health, which may include psychological counseling and lifestyle modifications. It is not an aphrodisiac and does not directly increase libido, but rather facilitates the physical response to sexual stimulation.
Features
- Active ingredient: Sildenafil citrate 100mg
- Pharmaceutical form: Film-coated tablet
- Mechanism: Selective inhibition of phosphodiesterase type 5 (PDE5)
- Onset of action: Approximately 30–60 minutes post-administration
- Duration of effect: Up to 4–6 hours
- Manufacturer: Produced under strict GMP (Good Manufacturing Practice) standards
Benefits
- Enhances genital blood flow, supporting natural lubrication and clitoral sensitivity
- May improve the ability to achieve and maintain physiological arousal
- Can contribute to more satisfying sexual experiences when psychological and relational factors are addressed
- Supported by clinical studies in women with diagnosed arousal disorders
- Offers a pharmacological option within a multimodal treatment plan
- May help reduce anxiety related to sexual performance by improving physical responsiveness
Common use
Lovegra is prescribed for adult women experiencing persistent, distressing difficulties with sexual arousal, often as part of a diagnosis such as female sexual arousal disorder (FSAD) or hypoactive sexual desire disorder (HSDD). It is used when reduced blood flow to the genital area is a contributing factor and where psychological, relational, or medical causes have been evaluated. It is not indicated for premenopausal or perimenopausal women without a specific clinical diagnosis, nor is it intended for recreational use. Patients are advised to use Lovegra only as part of an integrated treatment plan developed with a healthcare provider.
Dosage and direction
The standard dose is one 100mg tablet taken approximately 30–60 minutes before anticipated sexual activity. It should be swallowed whole with a glass of water; breaking or crushing the tablet is not recommended. Lovegra requires sexual stimulation to be effective. Do not exceed one dose in a 24-hour period. Dosage adjustments may be necessary for patients with hepatic impairment, severe renal impairment, or those taking certain concomitant medications—always follow the prescribing physician’s instructions.
Precautions
Before using Lovegra, disclose full medical history to your healthcare provider, especially regarding cardiovascular conditions, anatomical deformation of the penis (in partner), bleeding disorders, or retinitis pigmentosa. Avoid grapefruit juice, as it may increase sildenafil concentrations. Lovegra does not protect against sexually transmitted infections. Use with caution in patients with hypotension, hypertension, or recent history of stroke or myocardial infarction. Not recommended for use with other treatments for erectile dysfunction. Alcohol consumption may increase the risk of adverse effects such as dizziness or orthostatic hypotension.
Contraindications
Lovegra is contraindicated in patients with a known hypersensitivity to sildenafil or any excipients in the formulation. Concurrent use with organic nitrates (e.g., nitroglycerin, isosorbide mononitrate) or nitric oxide donors is strictly prohibited due to the risk of severe hypotension. It is also contraindicated in women with severe hepatic impairment, severe hypotension (BP < 90/50 mmHg), or recent history of stroke or myocardial infarction. Not for use in men or children.
Possible side effects
Common side effects may include headache, flushing, dyspepsia, nasal congestion, dizziness, and visual disturbances (such as altered color perception or blurred vision). Less frequently reported effects include nausea, rash, palpitations, and hypotension. In rare cases, priapism (prolonged and painful erection—relevant for male partners), sudden hearing loss, or non-arteritic anterior ischemic optic neuropathy (NAION) have been reported. Seek medical attention if any side effect is severe or persistent.
Drug interaction
Lovegra may interact with nitrates (contraindicated), alpha-blockers (increased hypotensive risk), CYP3A4 inhibitors (e.g., ketoconazole, ritonavir—may require dose adjustment), antihypertensive medications, and other PDE5 inhibitors. Concomitant use with recreational drugs containing nitrates (e.g., amyl nitrite) is dangerous. Always inform your prescriber of all medications, including over-the-counter drugs and herbal supplements.
Missed dose
Lovegra is not intended for regular daily dosing; it is taken on an as-needed basis. If a dose is missed, it may be taken later provided sufficient time remains before sexual activity (allow至少 30–60 minutes for onset). Do not double the dose to make up for a missed one.
Overdose
In case of suspected overdose, symptoms may include severe headache, profound hypotension, syncope, prolonged erection (in male partners), or visual disturbances. Seek immediate medical attention. Supportive measures should be implemented; haemodialysis is not expected to significantly enhance elimination.
Storage
Store below 25°C in the original packaging to protect from light and moisture. Keep out of reach of children and pets. Do not use after the expiration date printed on the packaging.
Disclaimer
This information is for educational purposes and does not replace professional medical advice. Lovegra is a prescription medication and should only be used under the supervision of a qualified healthcare provider. Individual results may vary. Not all users will experience the described benefits. Always follow your physician’s guidance regarding use, dosage, and potential risks.
Reviews
Clinical studies and patient reports indicate varied responses to Lovegra. Some women report improved arousal and satisfaction when the medication is used within a broader therapeutic context. Others note limited effect, particularly if psychological or relational issues are predominant. Effectiveness appears highest in women with clear physiological arousal deficits. Consistent with its mechanism, it does not enhance libido in the absence of sexual stimulation. Long-term safety data in women is less extensive than in men—ongoing monitoring and open communication with a healthcare provider are essential.