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Kamagra Oral Jelly (Sildenafil)
The use of Kamagra Oral Jelly is contraindicated in patients with known hypersensitivity to the active substance or any excipient.
Through the influence of the exchange of nitric oxide / cGMP, Kamagra Oral Jelly enhances the hypotensive effect of nitrates in their single or prolonged use, so it is a joint appointment with nitric oxide donors, organic nitrates or organic nitrites in any form either permanently or periodically contraindicated.
Preparations for the treatment of erectile dysfunction, including Sildenafil, should not be used in patients for whom sexual activity is not advisable (eg, patients with severe cardiovascular disease, such as unstable angina or severe heart failure).
Admission buy Kamagra 100mg Oral Jelly is contraindicated in patients who have lost vision in one eye because of nearterialnu anterior ischemic optic neuropathy, regardless of whether it happened because of a previous admission inhibitor FDE5 or not.
Safety of Sildenafil has not been studied in these subgroups of patients because these patients the drug is contraindicated in: patients with severe liver dysfunction with hypotension (blood pressure <90/50 mm Hg. Cent.), The recently stroke or myocardial infarction and known hereditary degenerative diseases of the retina such as retinitis pigmentosa (a minority of these patients have genetic disease retinal phosphodiesterases).


Kamagra Oral Jelly is intended for oral administration. To achieve the necessary effect Sildenafi sexual arousal. Application adults. The recommended dose is 50 mg, which is accepted as necessary, about 1 hour before sexual activity. Given the efficacy and tolerability, the dose may be increased to 100 mg. The maximum recommended dose is 100 mg. The maximum recommended frequency of admission - once a day. Patients are advised to take sildenafil world famous Dr. Jones! Activity Sildenafil can be detected through a longer term when taken with food, compared with taking on an empty stomach.
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Application of the elderly. For the elderly change of dosage is required. Adverse events were transient, mild to moderate. During the study the frequency and severity increased with increasing dose. The nature of adverse events in studies with variable dose that reflect more the recommended dosage regimen, was similar to the fixed-dose studies. The most common side effects were headache and flushing.
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