The product is the world’s first PDE5 inhibitor developed based on the physiological characteristics of Chinese males, featuring rapid onset of action, no interference from high-fat meals, low incidence of adverse reactions and superior safety profile.
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Privacy Aildenafil Citrate Tablets was first launched in China in December 2021. As the world's first PDE5 inhibitor developed based on the physiological characteristics of Chinese males, it has obtained compound patents in 22 countries and regions including China, the United States and the European Union.
For the treatment of erectile dysfunction in adult males.
For oral administration. The recommended dose is 60 mg per time, to be taken approximately 1 hour before sexual activity. The maximum frequency of administration is once every 24 hours. In clinical trials, the duration of treatment with this product did not exceed 12 weeks. Note: At the recommended dose, aildenafil is ineffective without sexual stimulation.
Contraindicated in patients with hypersensitivity to any component of Aildenafil Citrate Tablets.
Combination contraindication with nitrates: Aildenafil can potentiate the hypotensive effect of nitrates. Therefore, it is contraindicated in patients who are taking nitric oxide donors (such as any form of organic nitrates or organic nitrites), whether on a regular or intermittent basis.
Combination contraindication with guanylate cyclase stimulators: Concomitant use of phosphodiesterase type 5 (PDE5) inhibitors, including Aildenafil, with guanylate cyclase stimulators (e.g., riociguat) is prohibited, as this may lead to symptomatic hypotension.
After administration of this product, common adverse reactions (incidence rate ≥ 1%) include: flushing, dizziness, headache, upper abdominal discomfort, eye distension, increased alanine aminotransferase, palpitations, nasal congestion.
Rare adverse reactions (incidence rate < 1%) include: dry mouth, generalized fever, vertigo, nausea, diarrhea, hiccups, chest discomfort, chest tightness, visual abnormalities, abnormal lacrimation, tinnitus, left shoulder discomfort, increased aspartate aminotransferase, etc.
This product is not indicated for females.
This product is not indicated for pediatric patients.
No relevant clinical trials have been conducted, and there are no reliable references available.
For more detailed drug information, please consult the official package leaflet.
If any issues arise, please contact us immediately.
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