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Anlodipin

Anlodipin is a calcium channel blocker that dilates (widens) blood vessels and improves blood flow. Lowering blood pressure may lower your risk of a stroke or heart attack. Anlodipin is used to treat chest pain (angina) and other conditions caused by coronary artery disease. Anlodipin is also used to treat high blood pressure (hypertension).

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Also known as: Amlodipine

Description

Anlodipin is created by pharmacy specialists to combat angina and hypertension diseases. Target of Anlodipin is to control chest pain and decrease level of blood pressure. Anlodipin acts as an anti-angina and anti-hypertension remedy. Anlodipin operates by reducing blood pressure and regulating chest pain through blood provision to the heart. You can take Anlodipin in combination with other anti-hypertension preparations. Anlodipin is also known as Amlodipine besylate, Amlip, Avacard, Dailyvasc, Istin, Perivasc. Anlodipin is calcium channel blocker. Generic name of Anlodipin is Amlodipine. Brand name of Anlodipin is Anlodipin.

Dosage

Take Anlodipin exactly as prescribed by your doctor. Follow all directions on your prescription label. Your doctor may occasionally change your dose. Do not use this medicine in larger or smaller amounts or for longer than recommended.

You may take Anlodipin with or without food. Take the medicine at the same time each day.

Your blood pressure will need to be checked often.

Your chest pain may become worse when you first start taking Anlodipin or when your dose is increased. Call your doctor if your chest pain is severe or ongoing.

If you are being treated for high blood pressure, keep using Anlodipin even if you feel well. High blood pressure often has no symptoms. You may need to use blood pressure medicine for the rest of your life.

Your hypertension or heart condition may be treated with a combination of drugs. Use all medications as directed by your doctor. Read the medication guide or patient instructions provided with each medication. Do not change your doses or stop taking any of your medications without your doctor's advice. This is especially important if you also take nitroglycerin.

Anlodipin is only part of a complete program of treatment that may also include diet, exercise, weight control, and other medications. Follow your diet, medication, and exercise routines very closely.

Store at room temperature away from moisture, heat, and light.

Detailed Anlodipin dosage information

Overdose

If you overdose Anlodipin and you don't feel good you should visit your doctor or health care provider immediately. Symptoms of Anlodipin overdosage: fainting, dizziness, rapid heartbeat.

Storage

Store at room temperature between 15 and 30 degrees C (59 and 86 degrees F) away from moisture, light and heat. Keep container tightly closed. Throw away any unused medicine after the expiration date. Keep out of the reach of children in a container that small children cannot open.

Side effects

The most common side effects associated with Anlodipin are:

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Side effect occurrence does not only depend on medication you are taking, but also on your overall health and other factors.

Contraindications

Do not take Anlodipin if you are allergic to Anlodipin components. Do not take Anlodipin if you're pregnant or you plan to have a baby. Do not use it if you are a nursing mother. Do not use Anlodipin in case of suffering from significant aortic stenosis, cardiogenic shock, and unstable angina. Try to be careful with Anlodipin usage in case of having liver disease, heart failure or hepatic impairment. Do not use potassium supplements or salt substitutes. If you want to achieve most effective results without any side effects it is better to avoid alcohol. Be very careful when you are driving machine. Do not stop taking Anlodipin suddenly.

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But historians have recently shown how they play a number of roles that can illuminate different aspects of the history of science, from priority disputes to pedagogical practices. The cellular counterparts that can functionally substitute for viral RR and the carboxyl-terminal domain of ICP34.5 are cellular RR and the corresponding homologous domain of the growth arrest and DNA damage protein 34 (GADD34), respectively. That MDR resistance can enhance growth and survival in acid is an important consideration for enteric organisms passing through the acidic stomach. Key issues related to improving communication and the availability of appropriate evidence-based information on primary, secondary and tertiary prevention. 85-year-old woman being struck on her cheek and anterior chest, visited our emergency room. Another patient suffered progressive asymmetric paraparesis which first stabilized and later improved partially after surgical treatment of the aneurysm. The Yucatan mini-pig may be valuable as a model to determine the efficacy of prophylactic and therapeutic regimes. The purpose of this study was to assess reading level, tobacco knowledge, attitudes, and practices of tobacco use among pregnant adult and adolescent women in the public health system in north Louisiana. The necessity of each functional substructure of the carrier system for a specific and efficient gene silencing was confirmed. Idiopathic hyperCKemia and malignant hyperthermia susceptibility.

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Simultaneous management of tuberculum sellae meningioma and moyamoya disease was performed using left modified pterional incision. These changes indicate hyperactive mitochondrial replication in 143B cells. The aim of this study was to investigate the HLA-G serum levels in Primary Antiphospholipid Syndrome (PAPS) patients, its impact on clinical and laboratory findings, and heparin treatment. This study presents comparisons of two estimation methods of additive-by-additive interactions of QTL effects by the Monte Carlo simulation study. Data analysis was conducted for three subgroups: anterior, posterior, and anterior and/or heart medication amiodarone side effects posterior repair (not reported separately). Examiner placement of head position was achieved with inclinometers and triangulation. Several other cases of cryptosporidial diarrhea subsequently developed during a 1-month period. Mutagenesis of selected conserved amino acid residues of all three rotor components (cR45, cQ46, gammaE204, gammaF203 and epsilonH38) severely affected rotor assembly. No cooperative or additional contributions to the interaction were observed for Z-repeat double constructs.

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