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Belnif (Nifedipine)
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Belnif

Belnif is used to treat high blood pressure or angina (chest pain). For high blood pressure: Belnif works by relaxing and expanding the blood vessels. This makes the blood flow more easily and lowers blood pressure. Lower blood pressure reduces the strain on your heart. For angina: Belnif works by relaxing and expanding the arteries supplying the heart. This allows more blood and oxygen to reach the heart and decreases the strain on it. Your angina attacks will be less severe and less frequent if there is less strain on the heart.

Other names for this medication:
Cardifen, Cardiosol, Cardipin, Cardules, Casanmil, Cordaflex, Cordalat, Corinfar, Emaberin, Hexadilat, Myogard, Nelapine, Nidicard, Nifeclair, Nifed, Nifedel, Nifedipine, Nifedipress, Nifelat, Nifestad, Nifin, Noviken, Oxcord, Pressolat, Sepamit, Sidalat, Vasdalat

Similar Products:
Cymbalta, Minocin, Arimidex, Geodon, Neoral, Rulide

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Also known as: Nifedipine

Description

Nifedipine is used alone or together with other medicines to treat severe chest pain (angina) or high blood pressure (hypertension). High blood pressure adds to the workload of the heart and arteries. If it continues for a long time, the heart and arteries may not function properly. This can damage the blood vessels of the brain, heart, and kidneys, resulting in a stroke, heart failure, or kidney failure. High blood pressure may also increase the risk of heart attacks. These problems may be less likely to occur if blood pressure is controlled.

Nifedipine is a calcium channel blocker. It works by affecting the movement of calcium into the cells of the heart and blood vessels. As a result, nifedipine relaxes blood vessels and increases the supply of blood and oxygen to the heart while reducing its workload.

This medicine is available only with your doctor's prescription.

Dosage

This section provides information on the proper use of a number of products that contain nifedipine. It may not be specific to Belnif PA 20. Please read with care.

In addition to the use of this medicine, treatment for your high blood pressure may include weight control and changes in the types of foods you eat, especially foods high in sodium (salt). Your doctor will tell you which of these are most important for you. You should check with your doctor before changing your diet.

Many patients who have high blood pressure will not notice any signs of the problem. In fact, many may feel normal. It is very important that you take your medicine exactly as directed and that you keep your appointments with your doctor even if you feel well.

Remember that this medicine will not cure your high blood pressure, but it does help control it. You must continue to take it as directed if you expect to lower your blood pressure and keep it down. You may have to take high blood pressure medicine for the rest of your life. If high blood pressure is not treated, it can cause serious problems such as heart failure, blood vessel disease, stroke, or kidney disease.

Swallow the extended release tablet whole. Do not break, crush, or chew it. It is best to take this tablet on an empty stomach.

If you are taking the extended-release tablets, part of the tablet may pass into your stool after your body has absorbed the medicine. This is normal and nothing to worry about.

The dose of this medicine will be different for different patients. Follow your doctor's orders or the directions on the label. The following information includes only the average doses of this medicine. If your dose is different, do not change it unless your doctor tells you to do so.

The amount of medicine that you take depends on the strength of the medicine. Also, the number of doses you take each day, the time allowed between doses, and the length of time you take the medicine depend on the medical problem for which you are using the medicine.

For treatment of chest pain or high blood pressure: For oral dosage form (capsules): Adults—At first, 10 milligrams (mg) three times a day. Your doctor may increase your dose as needed. Children—Use and dose must be determined by your doctor. For oral dosage form (extended-release tablets): Adults—At first, 30 or 60 milligrams (mg) once a day. Your doctor may increase your dose as needed. However, the dose is usually not more than 90 mg once a day. Children—Use and dose must be determined by your doctor.

Overdose

If you overdose Belnif and you don't feel good you should visit your doctor or health care provider immediately.

Storage

Store the medicine in a closed container at room temperature, away from heat, moisture, and direct light. Keep from freezing.

Keep out of the reach of children.

Do not keep outdated medicine or medicine no longer needed.

Ask your healthcare professional how you should dispose of any medicine you do not use.

Detailed Nifedipine dosage information

Side effects

The most common side effects associated with Belnif 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 Belnif if you are allergic to Belnif components. Do not take Belnif if you're pregnant or you plan to have a baby, or you are a nursing mother. Belnif can harm your baby. Do not use Belnif in combination with salt substitutes or potassium supplements. If you want to achieve most effective results without any side effects it is better to avoid alcohol. Avoid grapefruit juice during treatment with Belnif. Try to be careful using Belnif if you suffer from kidney disease, liver disease, diseases of the heart or blood vessels (sick sinus syndrome), aortic stenosis, heart failure, low blood pressure, or coronary artery disease. Do not stop taking Belnif suddenly.

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Regional differences in postweaning growth by choroid plexuses as affected by dietary salt deficiencies. Human prenatal palatal closure related to skeletal maturity of the jaws. Vaccination with a protein antigen gave rise to serum and local antibody production. Variability of euchromatic and heterochromatic regions of Y chromosome in two types of cancer patients. One of the FAS clones ( FAS2 ) produces immunologically cross-reacting material in Escherichia coli. Passive immuno-gene therapy, employing an adoptive treatment with in vitro activated and expanded anti-tumor effector cells, involves two major application fields for gene transfer techniques, first the genetic modification of the effector cells, and second the in vivo amplification of pre-effector cells by procedures also used in active immuno-gene therapy. The temporomandibular joint pain-dysfunction syndrome has received little attention in the literature on pediatric neurology.

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Mycobacterium tuberculosis resistance to rifampicin and ethambutol: a clinical survey. The clinical presentation is similar to that of osteitis pubis, which is a self-limiting condition. The incidence of pinguecula and spheroid degeneration are correlated per site and per subject in the two geographically different series. The serum level of non-esterified fatty acid was high for one week while the triglyceride level was maintained at a high level only in the early post-operative period. Recent developments in the biologic production of ammonia and the use of ammonia and carbamide in caries prevention. Tympanometry was found to give unpredictable results and was unhelpful in assessing middle ear function in these patients. Engineering Pichia pastoris for biocatalysis: co-production of two active enzymes.

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Liver enlargement induced by the herbicide 2,4,5-trichlorophenoxyacetic acid (2,4,5-T). A ten-year follow-up of driving patterns among community-dwelling elderly. The gerbil MLR resembles MLRs recorded under similar conditions in guinea pig, cat, and rat. Glucose tolerance was not only decreased but also increased in the fasting state in de novo hypertension in late pregnancy due to a high insulin response. Blockade of oral morphine consumption in the male albino zofran dosage when pregnant rat by hypophysectomy. Stuttering: an investigation into cerebral dominance for speech. Compared with the nerve growth factors from the venoms of other Elapidae, namely Naja naja and Naja naja atra, this protein showed high isoelectric point of approximately pH 10. The limits of quantitation of lactone and total drug were 3 ng/ml in plasma and a linear range of determination were observed over the concentration of 3 to 500 ng/ml.

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