A selective calcium channel blockers; a derivative of dihydropyridine; has a vasodilating, antihypertensive, antianginal effect. Has a high selective activity against smooth muscle of the arterioles. Prescribed to the patients with hypertension, angina pectoris (voltage, vasospastic, unstable with the ineffectiveness of beta-blockers and nitrates), Raynaud's syndrome (as a symptomatic drug).
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Plendil Product Description
Drug Uses
Plendil is a calcium channel blocker, used to treat hypertension (high blood pressure). Antihypertensive drug Plendil relaxes the blood vessels, thus increasing the blood flow and lowwering the blood pressure.
Because Plendil has no effect on the venous smooth muscle, the antihypertensive drug does not cause orthostatic hypotension (colloquially as head rush).
Calcium channel blocker Plendil is prescribed to adults and elderly patients for treatment of hypertension and prophylaxis of chronic stable angina pectoris. To treat high blood pressure, an initial recommended Plendil dose is 5 mg per day.
Depending on the tolerability and the effect, the daily dose of Plendil can be increased up to 10mg or decreased to 2.5mg. If necessary, therapy with Plendil can be supported with another antihypertensive agent. The recommended maintenance Plendil dose is 5-10mg per day.
Missed dose
If more than 12 hours has passed after a missed dose of Plendil, do not take the calcium antagonist. In this case just return to the regular dosing schedule of Plendil.
More Information
Plendil is completely absorbed from the gastrointestinal tract and immediately provides an antihypertensive effect, which lasts about 2-5 hours. At the systematic application of antihypertensive agent Plendil, substantial control of blood pressure lasts for 24 hours. Plendil is well tolerated by the patients with renal transplant and requires no modification of the recommended dosage in patients with renal impairment.
Storage
Antihypertensive Plendil agent should be stored in a dark place in a tightly closed container, at room temperature not exceeding 25°C.
Plendil Safety Information
Warnings
Plendil is recommended to be indicated with caution to the hypertensive patients with heart failure. Coadministration of the calcium channel blocker with beta-adrenergic blocking agents is especially recommended to be avoided.
In some cases, the hypertension treatment in the patients with coronary artery disease may cause significant hypotension and result in myocardial ischaemia. Therefore, the level of blood pressure is recommended to be thoroughly monitored in these patients during the antihypertensive therapy with Plendil. Also the patients with a history of cerebrovascular insufficiency should be careful and try to avoid hypotension.
Disclaimer
This review of Plendil contains only general information on the hypertension treatment. This information in no case should be treated as medical advice from the cardiologist or other professional healthcare provider. The online pharmacy shall not be liable for any loss or damage, caused due to improper use of the information provided on antihypertensive agent Plendil.
Plendil Side Effects
Adverse effects after the application of Plendil are usually transient and decrease when dosages are decreased. Only about 6% of patients taking Plendil, have to discontinue the treatment due to blushing, ankle edema and headache. Other common and the most serious adverse effects after the use of Plendil are: nausea, dizziness, vomiting, weakness, palpitation, flush, gingival overgrowth, paraesthesia, low blood pressure, costiveness or paresthesia.
Avapro - the remedy which is used separately or in combination with other drugs for treatment of high blood pressure. It is also used for treatment of diseases of kidneys caused by diabetes mellitus 2 type (the state at which the organism can't use insulin normally and, therefore, can't control amount of sugar in blood) and high blood pressure. Irbesartan in a class of the drugs called antagonists of receptors of angiotensin II. It works by blocking of effects of some natural substances which tighten blood vessels that allows blood flow more smoothly and the heart works more effectively.
Cialis Soft Tabs differs from a usual tablet of Cialis in the fact that its action comes quicker. Cialis Soft is chewed and dissolved under a tongue that allows to reach a required effect in 10-15 minutes. Important!!! Cialis Soft is compatible to alcohol and greasy food!
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Copegus - antiviral medicine. Quickly gets into cells and works in the cells infected with a virus. Most sensitive to a ribavtrin, DNA viruses - a herpes simplex virus, viruses of group of smallpox, Marek's disease; RNA viruses - influenza viruses A, B, paramyxoviruses (parainfluenza, epidemic parotitis, the Newcastle disease), reoviruses, oncogenous RNA viruses.
Enhances the protective mechanisms of the gastric mucosa by increasing the formation of gastric mucus and of glycoproteins in it, as well as stimulation of bicarbonate secretion and endogenous Pg synthesis in it, promotes healing of its injuries (including scarring of stress ulcers), and the cessation of gastrointestinal bleeding. The list of indications includes: gastric ulcer and duodenal ulcer, hyperacidity of gastric juice, heartburn (associated with hyperchlorhydria), symptomatic and stress ulcers of the gastrointestinal tract.
An oral hypoglycemic means, which inhibiting the intestinal alpha-glycosidase, reduces the enzymatic conversion of di-, oligo - and polysaccharides to mono-saccharides, thereby reducing the absorption of glucose from the intestine and postprandial hyperglycemia. It is used to treat diabetes, of type 2 under the ineffective diet, the course of which shall not be less than 6 months, type 1diabetes within the combination therapy.
Enzymes for inward, affect edema of instigative and non-inflammatory origin (traumatic, sports). Animal studies have shown the anti-inflammatory characteristics of Benzac and mixed enzyme preparations in oral administration. In numerous animal studies, bromelain and trypsin suppressed platelet aggregation. Healthy volunteers who received a combination these substances were not observed to have a violation of the system of the ability of blood to thicken.
