Characteristic | Description |
---|---|
Active Ingredient | Sildenafil Citrate |
Dosage Forms | 50 mg, 100 mg |
Route of Administration | Oral |
Indication | Female Sexual Arousal Disorder |
Onset of Action | 30-60 minutes |
Duration of Effect | 4-6 hours |
More about Femalegra |
Pharmacokinetics
The pharmacokinetic profile of Femalegra involves the active ingredient, sildenafil citrate, commonly associated with erectile dysfunction treatment in men. Following oral administration, sildenafil is rapidly absorbed. Peak plasma concentrations occur within 30 to 120 minutes. The absolute bioavailability is approximately 41%, influenced by hepatic first-pass metabolism. The presence of high-fat meals can delay absorption, reducing peak concentration.
Sildenafil has a volume of distribution of about 105 liters, indicating extensive tissue distribution. It is predominantly metabolized in the liver by cytochrome P450 enzymes, mainly CYP3A4 and CYP2C9. The primary circulating metabolite, N-desmethylsildenafil, shares similar properties but exhibits only 50% potency. Approximately 80% of the administered dose is excreted as metabolites in feces and urine. The terminal half-life of sildenafil in healthy volunteers ranges between 3 to 5 hours.
Dosage Information
Femalegra, available in 50 mg and 100 mg tablets, requires tailored dosing for efficacy and safety. Initiation of treatment should start at the lower dose, with adjustments based on individual response and tolerability. Administer once daily, ideally one hour before sexual activity. A maximum recommended dose is 100 mg per day.
Patients with renal or hepatic impairment may require dose adjustments due to altered drug clearance. In such cases, healthcare professionals should assess the need for lower starting doses. Concomitant administration with potent CYP3A4 inhibitors warrants caution, as these can significantly increase sildenafil levels. Always consult with healthcare providers before any dosage modification.
Who Can and Cannot Take Femalegra
Femalegra suits adult females experiencing sexual arousal difficulties. However, certain populations should avoid its use. Patients with cardiovascular conditions, such as severe heart disease or recent myocardial infarction, face increased risks. It is contraindicated in those with hypersensitivity to sildenafil or any formulation excipients.
Those undergoing nitrate therapy or guanylate cyclase stimulators must avoid Femalegra due to profound hypotensive effects. Special consideration should apply to women with retinal disorders like retinitis pigmentosa, due to the possibility of vision impairment. Medical professionals must evaluate benefits versus risks in such scenarios. Read more about these contraindications here.
Femalegra Disposal
Safe disposal of Femalegra is paramount to prevent accidental ingestion or environmental contamination. Keep medications out of reach of children and pets. Do not flush tablets down the toilet unless specific disposal instructions indicate otherwise.
Engage with local pharmacy take-back programs when possible. These initiatives ensure environmentally friendly disposal. Consult pharmacists for guidance on community resources. When take-back options are unavailable, mix the tablets with unpalatable substances like used coffee grounds or cat litter. Secure in a sealed plastic bag and discard in household trash.
Femalegra Signs and Symptoms of Overdose
Overdose with Femalegra may provoke severe symptoms, necessitating immediate medical attention. Cardiovascular manifestations like hypotension or tachycardia can occur. Patients may experience visual disturbances, including blurred vision or sudden loss of vision.
Gastrointestinal effects such as nausea or vomiting might manifest. In rare cases, prolonged erections or priapism may present, requiring emergency care to prevent permanent damage. If overdose is suspected, seek medical help immediately. Symptomatic and supportive treatment remains the primary approach.
Is Non-prescription Femalegra Available?
Femalegra, as a medication containing sildenafil, requires a prescription. Regulatory guidelines ensure patient safety and therapeutic efficacy. Prescription status mandates professional evaluation before use. This ensures suitability based on individual health profiles.
Non-prescription variants lack assurance of efficacy and safety. They may carry risks of contamination or inappropriate dosage. Healthcare professionals emphasize obtaining medications from authorized sources. Always adhere to medical guidance to safeguard health.
Source:
- https://www.911mg.org/erectile-dysfunction/tadalis.htm
- https://elitinscorp.com/terapias-inovadoras-o-papel-de-kymriah-no-combate-a-bartonella-bacilliformis/
- https://nilkanthdham.org/optiray-injection-in-radiographic-imaging/
- https://autoescolametodo.com.br/beneficios-da-injecao-de-mecassermina-na-doenca-renal-cronica-drc/
- https://www.design-prinz.de/neuropathien-des-plexus-brachialis-und-medizinische-erkenntnisse/
- https://pavluc.nl/tenofovir-alafenamide-tablets-in-hiv-management-strategies/
- https://tscosmeticseg.com/2024/09/19/diltiazem-cd-cap24/
- https://copypro.fr/infection-a-cystoisospora-cystoisosporose/
- https://www.obsessionshop.es/2023/12/03/cancer-de-cuello-uterino-una-mirada-mas-amplia-al-tratamiento-de-infecciones-pediatricas/
- https://utlwanang.co.za/2024/06/28/infumorph-in-the-treatment-of-dog-bites-effective/
No responses yet