An antiaggregant, used for the prevention of thrombotic complications in patients with acute coronary syndrome (ACS), who are planned to undergo percutaneous coronary angioplasty and for prevention of stent thrombosis in acute coronary syndromes. The medicine is a receptor antagonist of P2Y12class to adenosine diphosphate (ADP), and consequently inhibits the activation and aggregation of platelets. Since platelets are involved in the development of atherosclerosis complications, the inhibition of platelet function may lead to a decrease in the frequency of cardiovascular complications.
Prasugrel
| Package | pill | Total price | Save | Order |
|---|---|---|---|---|
| 10mg × 30 Pills | $2.21 | $66.32 + Bonus - 4 Pills | - | Add to cart |
| 10mg × 60 Pills | $2.00 | $120.13 + Bonus - 4 Pills | $12.60 | Add to cart |
| 10mg × 90 Pills | $1.93 | $173.96 + Bonus - 7 Pills | $25.20 | Add to cart |
| 10mg × 120 Pills | $1.81 | $217.37 + Bonus - 7 Pills Free Trackable Delivery | $48.00 | Add to cart |
| 10mg × 180 Pills | $1.75 | $314.85 + Bonus - 11 Pills Free Trackable Delivery | $82.80 | Add to cart |
| 10mg × 360 Pills | $1.56 | $559.80 + Bonus - 11 Pills Free Trackable Delivery | $234.00 | Add to cart |
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Prasugrel product description
Refers to the clinical and pharmacological group of antiplatelet agents. This medication is a P2Y12 receptor antagonist to adenosine diphosphate. The effect of the drug is inhibition of activation and aggregation of platelets. Platelets take an active part in the development of the complication of atherosclerosis, platelet inhibition processes can lead to a significant reduction in the incidence of complications in the cardiovascular system of the patient. The process of drug exposure begins after 1-hour from the time of taking Prasugrel. Approximately 90% of patients within 1-hour show inhibition of platelet aggregation functions in 50% size. When taking the medication inward, Prasugrel is rapidly absorbed. Absorption processes are not dependent on eating, so the use of the medication is not limited to the mode of eating. The maximum concentration of the active substance in the blood serum of the patient is reached after 30 minutes from the time of taking the drug. The appointment and determination of dosages, as well as the duration of the course of treatment, should be performed by the treating healthcare specialist who knows the patient's medical history and can anticipate possible allergic reactions of the patient's organism to a particular stimulus in advance. Indications for the appointment of this medication can be a prevention of thrombotic complications in patients with an acute coronary syndrome, also for those who are scheduled to undergo percutaneous coronary angioplasty. This medical preparation can be prescribed for: unstable angina, myocardial infarction, as well as patients who will be assigned primary delayed percutaneous coronary angioplasty.
Prasugrel safety information
The medical care with Prasugrel begins with oral administration by the patient of a loading dosage equal to 60 mg, after which the drug is taken in a maintenance dosage of 10 mg once a day.
To prevent unwanted reactions, patients receiving Prasugrel in therapeutic muds should take acetylsalicylic acid from 75 to 325 mg.
The use of Prasugrel is not recommended in case you have some of the following contraindications : the condition of an increased risk of bleeding; a stroke in the anamnesis; impaired cerebral circulation; hepatic insufficiency of severe form; hypersensitivity to the active substance; deficiency of lactase in the patient's body; children and adolescents under 18; lactose intolerance; glucose-galactose malabsorption syndrome. The overdose of Prasugrel may lead to an increase in bleeding time and subsequent complications.
Prasugrel side effects
In order to avoid side effects and achieve maximum effectiveness from the treatment with Prasugrel, it is necessary to adhere to the dosage and the course of treatment prescribed by the healthcare specialist strictly. The following side effects may develop in patients: bleeding is possible; rectal bleeding; gastrointestinal bleeding; bleeding from the gums; bloody stools; hematoma at the site of the vascular puncture; rash; anemia; hemorrhage in the eye.
In case of an arterial hypertension of Atacand causes dose-dependent long lowering of arterial pressure. Anti-hypertensive action happens due to decrease in system peripheric resistance without reflex increase in heart rate. Instructions on serious or strengthened hypotension after taking of the first dose or Withdrawal Effect after termination of treatment are absent.
Viagra Super Active - an innovative formula of drug for treatment of erectile dysfunction. Drug is produced in gelatin capsules that allows to avoid emergence of heartburn or other unpleasant feelings in a stomach. Sildenafil Super Active also has a number of advantages. It is soaked quicker and works longer. The principle of action is identical with ordinary Sildenafil. Each capsule contains about 100 mg of active ingredient. That is quite enough for any man.
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Asendin, which is amoxapine, is used at treatment of major depressive disorder. In comparison with other antidepressants, it has more quick start of action, at the same time its therapeutic effects are observed from four to seven days. The drug also has the properties similar to atypical anti-psychotics, and can be used not on direct treatment of schizophrenia. Asendin - is a tetracyclic antidepressant from a family of dibenzoxazepine, however the drug is often classified as tricyclic antidepressant - of secondary amines.
Antidepressant. Strengthens the central adrenergic and serotonergic transfer. Used for the treatment of depressions including anhedonia, psychomotor retardation, insomnia, early awakening, weight loss, loss of interest in life, suicidal thoughts and mood swings.
Pamelor is a tricyclic antidepressant (TCA, tricyclic antidepressants) of the second generation. It is used in the treatment of some major depressive disorder and nocturnal enuresis (bedwetting) in children. In addition, the drug is sometimes used for the treatment of chronic diseases such as chronic fatigue syndrome, chronic pain and migraine, and the lability in certain neurological diseases.
It is a sulfonamide diuretic that is pharmacologically related to thiazide diuretics. The medicine inhibits sodium reabsorption in the cortical segment of the kidneys. It increases the excretion of sodium and chlorides in the urine and the excretion of potassium and magnesium, thus increasing diuresis. The antihypertensive effect of the active components appears at doses at which the diuretic effect is insignificant. Moreover, its antihypertensive effect persists even in patients with hypertension.
The drug has a thymoleptic and anxiolytic effect. Prescribed for the treatment of depressions of various origins, enuresis including the night one.
The anti-malarial drug from the group of 8-aminohinolina derivatives. It is characterized by intercalation with DNA plasmodia, leading to disruption of nucleic acids synthesis. It demonstrates high activity against exo-erythrocytic forms of all types of malaria, including primary tissue and para- erythrocyte forms. Particularly active against primary tissue forms of Plasmodium falciparum.
Gasex arranges the work of the intestine and reduces the time of digestion process. The drug acts as spasmolytic, antiulcerant, anti-inflammatory agent, cholagogue, hepatoprotective agent, membrane-modulating agent, an antimicrobial agent, and antioxidant. The drug also improves the digestibility of vitamins. It’s used for symptomatic control and relief of dyspepsia (upset stomach). The drug is used in case of flatulence, bloating, belching and for preliminary radiographic preparation of the intestine for radiography. The pills cope with discomfort in the abdomen in the postoperative period or during prolonged immobilization.
Product description
Alfacip is an active metabolite of Alfacip, which performs important functions in regulation of the calcium balance and the bone metabolism. (Hypocalcemia; Osteodystrophy; secondary hyperparathyroidism;)
