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
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|---|---|---|---|---|
| 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.
Clozaril - atypical antipsychotic medicine. Blocks dopamine receptors of CNS and interferes dopamine transfer in basal gangliya and in limbic part of neoncephalon. It is taken at Hypersensitivity, diseases of hemopoietic system (including in anamnesis), alcoholic and toxic psychosis, myasthenia, comas.
Brand Viagra - a drug from Pfizer, with a basic chemical called Sildenafil Citrate, is a first developed pharmaceutical to cure the difficulties with erection. It functions approximately within 4-5 hours, must be taken an hour prior to sex.
Cialis Super Active is a generic drug, against erectile dysfunction, containing 20 mg of tadalafil. The tablets in this series have a gel inside. This form allows the active substance, Tadalafil, to immediately enter the blood, thus providing an immediate effect. The result from the Cialis Super Active tablets appears after 5 minutes! The action lasts for two days. The drug is safe and has virtually no contraindications.
Accupril, which is quinapril, medication with hypotensive, natriuretic, cardio-protecting effect and vasodilating properties. It is used in case of an arterial hypertension (mono- or combined therapy), heart failure (combined therapy).
Aristocort - glucocorticoid drug (the adrenal hormone influencing carbohydrate and protein metabolism). Renders prominent antiinflammatory, antiallergic and immunodepressive (suppressing immunity - body defences of an organism) effect. It is prescribed at rheumatism, allergic reactions, multiform erythema (variously proceeding skin disease which occurs with rubefaction of affected area of skin), pseudorheumatism (the infectious and allergic disease from a group of collagenoses which is characterized by chronic progressing inflammation of joints); systemic lupus erythematosus and other collagenoses.
Cymbalta drug possesses a central mechanism of suppression of a pain syndrome that first of all can be noticed at increase in a threshold of painful sensitivity at pain syndrome of neuropathic etiology.
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.
Grifulvin V - the antifungal antibiotic, which is taken at mycoses of skin, hair and nails, and effective concerning fungus of the sort Trichophyton, Microsporum, Epydermophyton, Achorionum; causes disturbance of structure of mitotic spindle and synthesis of a cell wall in chitin fungus, suppresses division of fungal cells in metaphase and synthesis of protein because of disruption of linking with template-RNA.
An antifungal agent from the group of imidazole derivatives for external and local applications reduces the synthesis of ergosterol, which is a part of the cell membrane of the microbial wall and leads to a change in its structure and properties. In fungicidal concentrations, it interacts with mitochondrial and peroxidase enzymes, leading to an increase in the concentration of hydrogen peroxide to toxic levels, which also contributes to the destruction of fungal cells. The pills are active against pathogenic dermatophytes, pathogens of multi-colored lichen, erythrasma, gram-positive and gram-negative bacteria.
Zithromax - antibiotic of a wide spectrum of action. Antibiotic-azalide, a representative of a new subgroup of macrolide antibiotics. In the focus of inflammation it has a bactericidal effect. For the active ingredient of Zithromax, Azithromycin, all the gram-positive cocci (except those bacteria which are resistant to erythromycin) are susceptible.
Non-selective beta-blocker. Has antianginal, hypotensive and antiarrhythmic effect. It is used for arterial hypertension, angina pectoris, unstable angina, sinus tachycardia, supraventricular tachycardia, tachyarrhythmia, extrasystole.
Viagra Plus is the latest form of the medical treatment which is known worldwide. The formula is intensified by active medicinal plants, causing a boundless feeling of potentiality, unlimited desire and infinite lasting. The ginseng is one of the main ingredients of Viagra Plus, which carries out stimulation and increases endocrine activity in an organism, strengthens metabolism and facilitates cordial activity, helping thereby an arterial flow of blood, stimulating think-tanks and is promoted also by simplification of functioning of the central nervous system. Erection, sexual desire, success of sexual intercourse are guaranteed. From 400 mg of Viagra Plus - 50 mg make sildenafit, the remained 350 mg are ginseng and vitamins.
Levitra Soft - convenient chewable tablets, also act as their famous analogue - Brand Levitra, but cost several times cheaper. This form of generic tablet has a pleasant taste, it does not need to be taken with water. The effect occurs maximum in 15 minutes after taking the drug and lasts about 12 hours. The tablet can be combined with alcohol and fatty foods. The number of side effects is minimal and they are manifested only in cases of an overdose.
Gastroprotective agent, a synthetic analog of PgE1 boosts the formation of defensive slime and bicarbonate; enhances blood flow in the mucosa. It stimulates the healing of erosions, gastric and duodenal ulcers and is able to prevent their formation in some cases. It has a direct impact on the parietal cells of the abdomen, inhibits the lowest, and stimulated (by meal,pentagastrin, histamine) excretion of HCl. he drug diminishes the basal production of pepsin. The expected result occurs after 30 minutes and lasts at least 3-6 hours.
Florinef is a brand name of Fludrocortisone. It is a corticosteroid produced to treat adrenogenital syndrome (also called Apera-Galle syndrome), Addison's disease, orthostatic hypotension, cerebral salt wasting syndrome, and adrenal insufficiency. The drug replenishes the deficiency of hormones of the adrenal cortex. 1 tablet contains 0.1 mg of fludrocortisone acetate. It participates in the metabolism, including mineral and carbohydrate one. The drug causes the retention of sodium ions and promotes the excretion of potassium.
Nootropil improves cognitive processes, memory, attention, and mental performance.
Nootropilum affects the CNS, by changing the speed of propagation of the excitation in the brain, improves metabolic processes in nerve cells, improves by acting on the rheological characteristics of blood and causing no vasodilatory action.
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.
An antispasmodic drug, which removes pain and reduces the tone of smooth muscles: gastrointestinal tract, biliary tract, uterus, it also relaxes the detrusor (direct antispasmodic and m-anticholinergic effect). Increases bladder capacity, reduces the frequency of detrusor contractions, hinders urination. Well tolerated when appointed for a long term. Used in neurogenic bladder (including detrusor hyperreflexia, multiple sclerosis or spina bifida), urinary incontinence (of idiopathic origin), nocturnal enuresis (in children older than 5 years).
Tenorminis a cardioselective beta-adrenoblocker. It is based on a substance called Atenolol, which blocks nerve impulses, which leads to a decrease in the frequency and strength of the heartbeat. Atenolol has antihypertensive (lowers pressure), antianginal (eliminates the symptoms of myocardial ischemia) and antiarrhythmic (eliminates heart rhythm disturbances) by action.
Tadapox includes two medications combined for an even more effective approach of the problem of erectile dysfunction. The first one, Tadalafil, is a mighty restorative agent that reverses a male’s inability to achieve a satisfyingly firm erection. The second component, Dapoxetine, handles the other side of clinical impotency that shows as untimely ejaculation. Tadapox successfully manages said issues in populations of patients from 18 to 64 years of age. Its unique mix of therapeutic characteristics helps men revitalize their sexual function in a comparatively short time.
Pirfenex shows anti- fibrosing and anti-inflammatory properties in many systems in vitro and in animal models of pulmonary fibrosis (the fibrosis induced by bleomycin and transplantation). Assigned to adults suffering the idiopatic pulmonary fibrosis.
Betahistine is diaminoxidase inhibitor - the enzyme inactivating histamine. Stabilizing the histamine which is formed in an organism, betahistine has a histamine-like effect. Drug is effective at peroral taking (by mouth). Drug expands precapillary sphincters of vessels of an inner ear, it improves microcirculation. The main use of betahistine has at Menyer's disease and similar diseases which are followed by dizziness attacks, a sonitus, a hearing impairment, nausea, vomiting.
Xalatan is a chemical analog of the hormone prostaglandin. It is a topical agent available in the form of eye drops with a concentration of latanoprost 50 mcg/ml. Its mode of action is similar to the one of its natural equivalent – the drug increases the flow of intraocular fluid from the hypertensive eyeball. As a result, the pressure in the eyeball slowly decreases. Since this symptom frequently accompanies various eye diseases, Xalatan is often prescribed in combination with other medicines. Today, this drug is among the high-priority agents in the treatment of such an ubiquitous disease as glaucoma.
Xenical - a powerful, specific and reversible inhibitor of gastrointestinal lipases, which has a long-lasting effect. Its therapeutic effect is carried out in the lumen of the stomach and small intestine and consists in the formation of a covalent bond with the active serine portion of the gastric and pancreatic lipases. The inactivated enzyme at the same time loses the ability to break down food fats coming in the form of triglycerides, to sucking free fatty acids and monoglycerides. Since uncleaved triglycerides are not absorbed, the resulting decrease in the intake of calories into the body leads to a decrease in body weight. Thus, the therapeutic effect of the drug is carried out without absorption into the systemic circulation.
Fosamax - drug for treatment of Paget disease, osteoporosis at women in a postmenopause, osteoporosis at men, a hypercalcemia at malignant tumors. Active alendronate ingredient - non-hormonal specific inhibitor of an osteoclastic bone resorption, suppresses osteoclasts. Taking of Fosamax stimulates bone formation, recovers positive balance between a resorption and recovery of a bone, progressively increases the mineral density of bones, promotes formation of a normal bone tissue with normal histologic structure.
Arimidex, which is anastrozole - is prescribed for women in the post-menopausal period of widespread breast cancer. As exception can be patients with estrogen negative cancer if only earlier they didn't have a positive clinical answer on tamoxifen. For adjuvant therapy at the patients in the post-menopausal period having the positive indicators of receptor of hormone, an invasive estrogenpositive breast cancer at early stages. For adjuvant therapy at patients in a post-menopausal period who had adjuvant treatment by tamoxifen within 2-3 years, estrogen of a positive breast cancer at early stages.
Alprostadil is a medicine used to treat the symptoms of Erectile Dysfunction (impotence).
Peripheral vasodilator with predominant effect on venous vessels. Reduces the need for myocardium in oxygen by reducing preload and afterload (reduces the end diastolic volume of the LV and reduces the systolic tension of its walls). Has the coronary dilatation effect. Reduces blood flow to the right atrium, helps to reduce pressure in the "small" circle of blood circulation and regression of symptoms with pulmonary edema. Promotes redistribution of coronary blood flow in the area with reduced blood circulation. Increases tolerance to physical activity in patients with IHD, angina pectoris.
Voltaren Gel is an over the counter and prescription medicine used to treat symptoms of actinic keratosis, osteoarthritis, acute pain and arthritis pain. Voltaren Gel may be used alone or with other medications.
Voltaren Gel belongs to a class of drugs called Topical Skin Products.
Sildamax working with the phosphodiesterase type5 inhibitor. which happening a quicker and more grounded blood flow. That move through the guy’s genital region abandoning him with a harder erection. Sildamax tablets might be a medicine that’s alleged to be take. It’s a generic medication provides you with Associate during a Nursing erection.