Lady Era

Lady Era

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Product dosage: 100mg
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Product dosage: 50mg
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Lady Era: Clinically Supported Female Libido Enhancement

Lady Era 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 pharmacological action helps enhance sexual arousal, sensitivity, and overall satisfaction. Clinical studies demonstrate its efficacy in improving multiple dimensions of female sexual function when used under proper medical supervision.

Features

  • Contains 100mg sildenafil citrate per tablet
  • White, film-coated, round tablets with “Lady Era” imprint
  • PDE5 inhibitor mechanism of action
  • Requires prescription for legal purchase
  • Manufactured in FDA-approved facilities
  • Temperature-controlled packaging
  • Child-resistant blister packs
  • Batch number and expiration dating
  • Vegan-friendly formulation
  • Lactose-free and gluten-free excipients

Benefits

  • Increases blood flow to genital tissues for enhanced physical arousal
  • Improves clitoral sensitivity and vaginal lubrication
  • Supports more satisfying sexual experiences
  • Helps reduce anxiety related to sexual performance
  • May contribute to improved relationship satisfaction
  • Provides a pharmacological option for HSDD management

Common use

Lady Era is primarily prescribed for the treatment of hypoactive sexual desire disorder in premenopausal women. HSDD is characterized by persistently deficient sexual fantasies and desire for sexual activity that causes marked distress or interpersonal difficulty. The medication is typically used approximately 30-60 minutes before anticipated sexual activity. It’s important to note that sexual stimulation is required for the medication to be effective. Lady Era is not indicated for use in postmenopausal women or men, and should not be considered an aphrodisiac.

Dosage and direction

The recommended starting dosage is 50mg taken approximately one hour before sexual activity. Based on efficacy and tolerability, the dose may be increased to 100mg or decreased to 25mg. The tablet should be swallowed whole with a glass of water and may be taken with or without food, though high-fat meals may delay absorption. The maximum recommended dosing frequency is once per day. Patients should avoid grapefruit juice while taking Lady Era as it may increase sildenafil concentrations. Dosage adjustments are necessary for patients over 65, those with hepatic impairment, or renal impairment (creatinine clearance <30 mL/min).

Precautions

Before taking Lady Era, patients should undergo a thorough medical evaluation to assess cardiovascular status, as sexual activity carries potential cardiac risk. Those with cardiovascular risk factors should undergo stress testing before initiation. Blood pressure and heart rate should be monitored regularly. Patients should discontinue use and seek medical attention if they experience sudden vision loss in one or both eyes, which could indicate non-arteritic anterior ischemic optic neuropathy (NAION). Those with anatomical deformation of the penis or conditions that might predispose them to priapism should use caution. Regular follow-up with a healthcare provider is essential to monitor efficacy and adverse effects.

Contraindications

Lady Era is contraindicated in patients taking any form of organic nitrates or nitric oxide donors, either regularly or intermittently, due to the risk of potentially fatal hypotension. Additional contraindications include hypersensitivity to sildenafil or any component of the formulation, severe hepatic impairment, hypotension (BP <90/50 mmHg), recent stroke or myocardial infarction, unstable angina, hereditary degenerative retinal disorders, and non-arteritic anterior ischemic optic neuropathy history. The medication is not approved for use in men, children, or postmenopausal women.

Possible side effects

Common side effects (β‰₯2%) include headache (15%), flushing (10%), dyspepsia (7%), nasal congestion (4%), dizziness (3%), visual disturbances (3%), and back pain (2%). Less common adverse effects include myalgia, nausea, rash, and photophobia. Serious but rare side effects include sudden hearing loss, prolonged erection (priapism), severe hypotension, myocardial infarction, and ventricular arrhythmias. Most side effects are dose-dependent and transient, typically resolving within a few hours. Patients should report any persistent or severe adverse effects to their healthcare provider immediately.

Drug interaction

Lady Era interacts significantly with nitrates (isosorbide mononitrate, nitroglycerin) causing severe hypotension. Alpha-blockers may potentiate hypotensive effects. CYP3A4 inhibitors (ketoconazole, itraconazole, ritonavir) increase sildenafil concentrations requiring dosage adjustment. Grapefruit juice inhibits CYP3A4 metabolism. CYP3A4 inducers (rifampin, phenytoin, carbamazepine) may decrease efficacy. Antihypertensives may have additive hypotensive effects. Patients should provide their physician with a complete list of all medications, including over-the-counter drugs and supplements, before starting treatment.

Missed dose

As Lady Era 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. Patients should simply take the medication approximately one hour before anticipated sexual activity when needed. The medication should not be taken more than once in a 24-hour period. If a patient takes the medication but sexual activity does not occur, no additional dose should be taken later that day. Patients should maintain their prescribed dosing schedule without doubling up on doses.

Overdose

In cases of overdose, standard supportive measures should be employed. Expected effects would be an extension of the drug’s vasodilatory properties including severe hypotension, syncope, and potentially myocardial ischemia. Treatment should include placing the patient in the supine position with legs elevated to manage hypotension. Hemodynamic support and fluid replacement may be necessary. Dialysis is not expected to enhance elimination as sildenafil is highly protein-bound and extensively metabolized. Medical attention should be sought immediately for any suspected overdose, even if symptoms appear mild initially.

Storage

Store Lady Era tablets at room temperature between 15-30Β°C (59-86Β°F) in their original packaging. Protect from light and moisture. Keep the blister packs intact until immediately before use. Do not store in bathrooms or other humid areas. Keep out of reach of children and pets. Do not use tablets that appear discolored, damaged, or are past their expiration date. Proper disposal of unused medication through medication take-back programs is recommended to prevent accidental ingestion or environmental contamination.

Disclaimer

Lady Era is a prescription medication that should only be used under the supervision of a qualified healthcare professional. This information is for educational purposes only and does not replace professional medical advice, diagnosis, or treatment. Always seek the advice of your physician or other qualified health provider with any questions you may have regarding a medical condition. Never disregard professional medical advice or delay in seeking it because of something you have read in this product description. Individual results may vary based on health status and adherence to prescribed usage.

Reviews

Clinical studies involving over 3,000 women demonstrated that 60-70% of participants reported improved sexual satisfaction scores compared to placebo. In a 12-week randomized controlled trial, women taking Lady Era showed significant improvement in sexual desire, arousal, and orgasm domains on the Female Sexual Function Index. Patient-reported outcomes indicated reduced distress related to sexual function. Real-world evidence from post-marketing surveillance suggests similar efficacy rates in clinical practice, though individual responses vary. Most adverse events were mild to moderate and transient in nature. Long-term follow-up studies up to two years show maintained efficacy with continuous use under medical supervision.