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Bidinatec (Enalapril)
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Bidinatec

Bidinatec is used to treat high blood pressure. Lowering high blood pressure helps prevent strokes, heart attacks, and kidney problems. It is also used to treat heart failure and to help prevent people with a certain heart problem (left ventricular dysfunction) from developing heart failure. Bidinatec belongs to a class of drugs known as ACE inhibitors. It works by relaxing blood vessels so blood can flow more easily.

Other names for this medication:
Convertase, Cosil, Crinoren, Ditensil, Enadura, Enafril, Enaprel, Enapril, Enarenal, Enecal, Enetil, Epril, Herten, Hipertin, Hipoartel, Ileveran, Invoril, Lariludon, Nacor, Narapril, Renacardon, Selis, Tencas, Ulticadex, Unipril

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Avana, Vermox, Coreg, Ilosone, Ditropan, Forfora, Crolix, Radic, Hafenthyl, Aptaur, Tricort, Faceclin, Gallab, Kemadrin,

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Also known as: Enalapril

Description

Bidinatec (enalapril) is an ACE inhibitor. ACE stands for angiotensin converting enzyme.

Bidinatec is used to treat high blood pressure (hypertension) in adults and children who are at least 1 month old.

Bidinatec is also used to treat congestive heart failure in adults.

Bidinatec is also used to treat a disorder of the ventricles (the lower chambers of the heart that allow blood to flow out of the heart). This disorder can decrease the heart's ability to pump blood to the body.

Dosage

Usual Adult Dose for Hypertension:

Initial dose: 5 mg orally once a day Maintenance dose: 10 to 40 mg orally per day as a single dose or in 2 divided doses Maximum dose: 40 mg orally daily as a single dose or in 2 divided doses In combination with diuretics: Initial dose: 2.5 mg orally once a day If feasible, the diuretic should be discontinued 2 to 3 days prior to initiation of therapy with enalapril. If required, diuretic therapy may be gradually resumed.

Usual Adult Dose for Congestive Heart Failure:

Initial dose: 2.5 mg orally once a day Maintenance dose: 2.5 to 20 mg daily in 2 divided doses Maximum dose: 40 mg orally per day in 2 divided doses Comments: -Treatment is usually combined with diuretics and digitalis. -Doses should be titrated upward, as tolerated, over a period of a few days or weeks.

Usual Adult Dose for Left Ventricular Dysfunction:

Initial dose: 2.5 mg orally twice a day Maintenance dose: 20 mg orally per day in 2 divided doses Comments: -After the initial dose, the patient should be observed for at least 2 hours and until blood pressure has stabilized for at least an additional hour. -If possible, the dose of any concomitant diuretic should be reduced which may diminish the likelihood of hypotension.

Usual Pediatric Dose for Hypertension:

Children 1 month to 17 years: Initial dose: 0.08 mg/kg/day (up to 5 mg) in 1 to 2 divided doses. Adjust dosage based on patient response. Maximum dose: Doses greater than 0.58 mg/kg (40 mg) have not been evaluated in pediatric patients. Comment: -Not recommended in neonates and in pediatric patients with glomerular filtration rate less than 30 mL/min, as no data are available.

Detailed Bidinatec dosage information

Overdose

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

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 Bidinatec 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

Tell your doctor if you have ever had any unusual or allergic reaction to this medicine or any other medicines. Also tell your health care professional if you have any other types of allergies, such as to foods, dyes, preservatives, or animals. For non-prescription products, read the label or package ingredients carefully.

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Our studies indicate that the squamous epithelium is a suboptimal environment for growth, and thus potentially contributing to the protection of the lower genital tract from infection. Probing Mammalian Cell Size Homeostasis by Channel-Assisted Cell Reshaping. Muscle networks were extracted using coherence analysis of muscle activity assessed using surface electromyography (EMG). The OmpA protein level tested positive by western blot in clinical strains of A. The efficiency differences, depending on laser wavelengths, were discussed from the point of view of structural and environmental differences of light-absorbing groups. All membrane preparations displayed acetylcholinesterase activity (AChE, EC 3.1.1.7), this being relatively more concentrated in T-tubule membranes than in those derived from sarcoplasmic reticulum. ABO hemolytic disease of the fetus and newborn (ABO HDFN) may manifest itself in cases of mothers belonging to blood group O and newborns of groups A or B and more frequently in group A and less so in group B. However, it remains to be demonstrated that treatment of these lesions will improve the clinical outcome in BMT recipients without GI symptoms. Femoral neuropathy following abdominal operations for genitourinary malignancies. Effect of recombinant bactericidal/permeability-increasing protein on endotoxin translocation and lipopolysaccharide-binding protein/CD14 expression in rats after thermal injury.

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Glutamine may have similar qualities to histidine and be involved in the low susceptibility to autoxidation. Furthermore, replication of the second plasmid was increased when the first plasmid contained the T4 origin. We aimed to clarify the differences between these diseases, allowing accurate diagnosis based on their clinical features. The ability to use thoracic quantitative computed tomography (QCT) to detect the annual change of BMD remains unclear. A prepared complication furnishes the ratios of calcium to fluoride and calcium to phosphates in epiphysis and metaphysis parts, as well as ratio of calcium in epiphysis to calcium in metaphysis parts of the studied bones in the respective age groups. In the present study, we found that the nucleosome containing human H3T is significantly unstable both in vitro and in vivo, as compared to the conventional nucleosome containing H3.1.

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