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    It comes as immediate-release and extended-release oral tablets, and extended-release oral capsules. It also comes in an injectable form that’s only given by a healthcare provider. Metoprolol oral tablets are available as the brand-name drugs Lopressor and Toprol XL. Generic drugs usually cost less than the brand-name versions. In some cases, they may not be available in all strengths or forms as the brand-name drugs. The two brand-name forms of metoprolol (as well as the different generic forms) are different versions of the medication. They’re both metoprolol, but they contain different salt forms. The different salt forms enable the drugs to be used to treat different conditions. Metoprolol succinate is an extended-release version of metoprolol, so it remains in your bloodstream for a longer time. lasix to buy in the uk Switching from immediate-release to extended-release: Use same total daily dose of metoprolol Switching between oral and IV dosage forms: Equivalent beta-blocking effect is achieved in 2.5:1 (oral-to-IV) ratio Dizziness (10%) Headache (10%) Tiredness (10%) Depression (5%) Diarrhea (5%) Pruritus (5%) Bradycardia (9%) Rash (5%) Dyspnea (1-3%) Cold extremities (1%) Constipation (1%) Dyspepsia (1%) Heart failure (1%) Hypotension (1%) Nausea (1%) Flatulence (1%) Heartburn (1%) Xerostomia (1%) Wheezing (1%) Bronchospasm (1%) Anxiety/nervousness Hallusinations Paresthesia Hepatitis Vomiting Arthralgia Male impotence Reversible alopecia Agranulocytosis Dry eyes Worsening of psoriasis Pyronie’s disease Sweating Photosensitivity Taste disturbance Lopressor and Toprol XL only Ischemic heart disease may be exacerbated after abrupt withdrawal Hypersensitivity to catecholamines has been observed during withdrawal Exacerbation of angina and, in some cases, myocardial infarction (MI) may occur after abrupt discontinuance When long-term beta blocker therapy (particularly with ischemic heart disease) is discontinued, dosage should be gradually reduced over 1-2 weeks with careful monitoring If angina worsens markedly or acute coronary insufficiency develops, beta-blocker administration should be promptly reinitiated, at least temporarily (in addition to other measures appropriate for unstable angina) Patients should be warned against interruption or discontinuance of beta-blocker therapy without physician advice Because coronary artery disease (CAD) is common and may be unrecognized, beta-blocker therapy must be discontinued slowly, even in patients treated only for hypertension Use with caution in cerebrovascular insufficiency, CHF, cardiomegaly, myasthenia gravis, hyperthyroidism or thyrotoxicosis (may mask signs or symptoms), liver disease, renal impairment, peripheral vascular disease, psoriasis (may cause exacerbation of psoriasis) May exacerbate bronchospastic disease; monitor closely Beta blockers can cause myocardial depression and may precipitate heart failure and cardiogenic shock Sudden discontinuance can exacerbate angina and lead to MI and ventricular arrhythmias in patients with CAD Worsening cardiac failure may occur during up-titration of metoprolol succinate; if such symptoms occur, increase diuretics and restore clinical stability before advancing the dose of metoprolol succinate; it may be necessary to lower the dose of metoprolol succinate or temporarily discontinue it Bradycardia, including sinus pause, heart block, and cardiac arrest, has been reported; patients with 1° atrioventricular block, sinus node dysfunction, or conduction disorders may be at increased risk Increased risk of stroke after surgery May potentiate hypoglycemia in patients with diabetes mellitus and may mask signs and symptoms Avoid starting high-dose regimen of extended-release metoprolol in patients undergoing noncardiac surgery; use in patients with cardiovascular risk factors is associated with bradycardia, hypotension, stroke, and death Long-term beta blockers should not be routinely withdrawn before major surgery; however, impaired ability of the heart to respond to reflex adrenergic stimuli may augment risks of general anesthesia and surgical procedures Metoprolol loses beta-receptor selectivity at high doses and in poor metabolizers If drug is administered for tachycardia secondary to pheochromocytoma, it should be given in combination with an alpha blocker (which should be started before metoprolol is started) While taking beta blockers, patients with history of severe anaphylactic reaction to variety of allergens may be more reactive to repeated challenge Extended release tablet should not be withdrawn routinely prior to major surgery Hydrochlorothiazide, can cause an idiosyncratic reaction, resulting in acute transient myopia and acute angle-closure glaucoma, which can lead to permanent vision loss if not treated; discontinue hydrochlorothiazide as rapidly as possible if symptoms occur; prompt medical or surgical treatments may need to be considered if intraocular pressure remains uncontrolled; risk factors for developing acute angle-closure glaucoma may include history of sulfonamide or penicillin allergy Caution in patients with history of psychiatric illness; may cause or exacerbate CNS depression Beta-blockers can precipitate or aggravate symptoms of arterial insufficiency in patients with peripheral vascular disease There are no adequate and well-controlled studies in pregnant women Limited data on the use of metoprolol in pregnant women Risk to fetus/mother is unknown; because animal reproduction studies are not always predictive of human response, use if clearly needed Bioavailability: 40-50% (immediate-release) ; 65-77% (extended-release) relative to immediate release Onset: 20 min (IV), when infused over 10 min; onset may be immediate, depending on clinical setting; 1-2 hr (PO) Duration: 3-6 hr (PO); duration is dose-related; 24 hr (ER); 5-8 hr (IV) Peak plasma time: 1.5-2 hr (immediate-release); 3.3 hr (extended-release) Therapeutic range: 35-212 ng/m L The above information is provided for general informational and educational purposes only. Individual plans may vary and formulary information changes. Contact the applicable plan provider for the most current information.

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    Metoprolol to lek z grupy beta-adrenolityków, inaczej beta-brokerów. tabletki o przedłużonym uwalnianiu; 50 mg, 100 mg; 23,75 mg, 47,5 mg, 95 mg, 142,5 mg. metoprolol dizziness UpToDate, electronic clinical resource tool for physicians and patients that provides information on Adult Primary Care and Internal Medicine, Allergy and. Find patient medical information for Metoprolol Succinate Oral on WebMD including its uses, side effects and safety, interactions, pictures, warnings and user.

    Metoprolol to lek z grupy beta-adrenolityków, inaczej beta-brokerów. Oznacza to, że jego mechanizm działania polega na blokowaniu receptorów beta-adrenergicznych. Zażywanie metoprololu będzie powodowało zahamowanie aktywności układu współczulnego, którego aktywność powoduje zwężenie naczyń krwionośnych i tym samym wzrost ciśnienia krwi. Producent leku: różni producenci w zależności od preparatu Postać, dawka, opakowanie: tabletki powlekane, tabletki o przedłużonym uwalnianiu; 50 mg, 100 mg; 23,75 mg, 47,5 mg, 95 mg, 142,5 mg, 190 mg; opak. Kategoria dostępności: Rp – lek wydawany na receptęSubstancja czynna: winian metoprololu Podstawowym wskazaniem do stosowania metoprololu jest nadciśnienie tętnicze, ale również dławica piersiowa, kłopoty z układem sercowo-naczyniowym, a w szczególności częstoskurcz nadkomorowy czy zaburzenia rytmu serca. Metoprolol jest także wykorzystywany jako lek pomocniczy przy nadczynności tarczycy. Metoprolol stosowany jest również po zawale mięśnia sercowego, gdyż zmniejsza ryzyko powikłań (np. , pozbawiony wewnętrznej aktywności sympatykomimetycznej, wykazuje podobną siłę blokady receptorów jak propranolol. Po podaniu metoprololu w postaci o kontrolowanym uwalnianiu selektywność w stosunku do receptorów β. Metoprolol wykazuje nieznaczne działanie stabilizujące błonę komórkową. Osłabia działanie amin katecholowych uwalnianych podczas wysiłku fizycznego lub stresu i powoduje zmniejszenie częstotliwości rytmu serca, zmniejszenie pojemności minutowej i obniżenie ciśnienia tętniczego. Nie hamuje prawidłowych reakcji fizjologicznych w warunkach stresu, zachodzących pod wpływem adrenaliny uwolnionej z nadnerczy. W dawkach leczniczych w mniejszym stopniu powoduje skurcz mięśniówki oskrzeli niż niewybiórcze β-adrenolityki, co pozwala na stosowanie leku jednocześnie z β-mimetykami u chorych z astmą oskrzelową lub objawami POCh P. Przez zmniejszenie zapotrzebowania mięśnia sercowego na tlen zmniejsza częstość epizodów bólowych i zwiększa tolerancję wysiłku w dławicy piersiowej. Działanie β-adrenolityków może być również związane ze zmniejszeniem stymulacji adrenergicznej z ośrodków naczynioruchowych w mózgu.

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