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Cardinorm (Carvedilol)
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Cardinorm

Cardinorm is a non selective beta-adrenergic antagonist used to treat mild to severe chronic heart failure, hypertension, and left ventricular dysfunction following myocardial infarction in clinically stable patients. Cardinorm was granted FDA approval on 14 September 1995.

Other names for this medication:
Caarca, Caditone, Cadmos, Carca, Cardinorm, Cardivas, Cardol, Carelol, Carloc, Cartab, Carvas, Carvedil, Carvedilol, Carvel, Carvetrend, Carvibeta, Carvidac, Carviflo, Carvil, Carvimed, Carvipress, Carvistar, Carvizest, Carzec, Caslot, Cevas, Conpres, Coslot, Oricar, Vasicard

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Also known as: Carvedilol

Description

{name} (carvedilol) is a beta-blocker. Beta-blockers affect the heart and circulation (blood flow through arteries and veins).

{name} is used to treat heart failure and hypertension (high blood pressure).

{name} is also used after a heart attack that has caused your heart not to pump as well.

Dosage

Follow all directions on your prescription label and read all medication guides or instruction sheets. Your doctor may occasionally change your dose. Use the medicine exactly as directed.

Cardinorm CR works best if you take it with food, at the same time every day.

Swallow the extended-release capsule whole and do not crush, chew, break, or open it.

If you cannot swallow a capsule whole, open it and sprinkle the medicine into a spoonful of cold applesauce. Swallow the mixture right away without chewing. Do not save it for later use.

If you are switched from Cardinorm CR tablets to this medicine extended-release capsules (Cardinorm CR), your daily total dose of Cardinorm CR may be higher or lower than before. Older adults may be more likely to become dizzy or feel faint when switching from tablets to extended-release capsules. Follow your doctor's instructions.

Your blood pressure will need to be checked often.

If you need surgery (including cataract surgery), tell your surgeon you currently use this medicine. You may need to stop for a short time.

You should not stop using Cardinorm CR suddenly. Stopping suddenly may cause chest pain or a heart attack. Follow your doctor's instructions about tapering your dose.

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

Cardinorm CR is only part of a complete treatment program that may also include diet, exercise, and weight control. Follow your doctor's instructions very closely.

Store at room temperature away from moisture and heat.

Detailed Cardinorm CR dosage information

Overdose

If you overdose Cardinorm and you don't feel good you should visit your doctor or health care provider immediately. Symptoms of Cardinorm overdosage: bluish-colored fingernails, weakness, short breathing, fainting, uneven heartbeats, convulsions, lightheadedness.

Storage

Store at room temperature below 30 degrees C (86 degrees F) away from moisture and heat. Keep container tightly closed. Throw away any unused medicine after the expiration date. Keep out of the reach of children.

Side effects

The most common side effects associated with Cardinorm 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

Avoid driving or hazardous activity until you know how this medicine will affect you. Your reactions could be impaired. Avoid getting up too fast from a sitting or lying position, or you may feel dizzy.

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Metabolic impairments that precede type 2 diabetes, such as metabolic syndrome, may contribute to the development of chronic kidney disease (CKD). Offspring mass was negatively correlated with litter size, and the strength of this trade-off decreased with the degree of individual variation in resource acquisition, which confirms theoretical predictions. The Electrodiagnostic Neurophysiological Automated Analysis (ENAA) telematic system was developed in the EU EUREKA project. A molecular study of human leukocyte antigen associations was undertaken in patients with IDC to further explore the possibility of susceptibility markers of genetically determined disease. Then a diagnostic model was developed based on the logistic regression analysis.

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