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Budenase (Budesonide)
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Budenase

Budenase is not a rescue inhaler like albuterol. It works by reducing the inflammation and swelling of the airways in the lungs over time. It can take up to 2 to 6 weeks before you can feel the full effects.

Other names for this medication:
Airtec, Breemax, Bubate, Budamate, Budanase, Budate, Budecort, Budefex, Budenase, Budesal, Budesonide, Budetrol, Budez, Budvent, Bunase, Buovent, Derinide, Entocort, Foracort, Pulmicort, Symbicort

Similar Products:
Reminyl, Thorazine, Aldactone, Provigil, Lanoxin, Duphaston, Estrace, Priligy, Arava

Also known as: Budesonide

Description

Budenase is a corticosteroid. It works by shrinking swollen and inflamed nasal tissue, and by blocking the action of certain cells and chemicals of the immune system, thus reducing inflammation and swelling and so relieving congestion, itching, sneezing, irritation and discomfort. Budenase nasal spray is also used for nasal polyps, which are small growths inside the nose that can cause symptoms similar to allergic rhinitis. It is also used to keep nasal polyps from coming back after surgery to remove them. Generic name of Budenase is Budesonide. Budenase is also known as Budesonide, Budenase, Rhinosol.

Dosage

This section provides information on the proper use of a number of products that contain budesonide. It may not be specific to Budenase Turbuhaler. Please read with care.

Inhaled budesonide is used to prevent asthma attacks. It is not used to stop an attack that has already started. For relief of an asthma attack that has already started, you or your child should use another medicine. If you do not have another medicine to use for an acute asthma attack or if you have any questions about this, check with your doctor.

Use this medicine only as directed. Do not use more of it and do not use it more often than your doctor ordered. Also, do not stop taking this medicine without telling your doctor. To do so may increase the chance of side effects.

In order for this medicine to help prevent asthma attacks, it must be used every day in regularly spaced doses, as ordered by your doctor. This medicine usually begins to work in about 24 to 48 hours, but up to 2 to 6 weeks may pass before you feel the full effects.

Do not change your dose or stop using this medicine without first checking with your doctor. Your doctor may want you to gradually reduce the amount you are using before stopping it completely. Some conditions may become worse when the medicine is stopped suddenly, which can be dangerous.

When using the Pulmicort Flexhaler™:

This medicine comes as a powder that you breathe into the lungs with a special inhaler that is placed in the mouth. It is used by adults, teenagers, and children who are 6 years of age and older. The medicine comes with patient instructions. Read the instructions carefully before using this medicine. If you or your child do not understand the instructions or are not sure how to use the inhaler, check with your doctor. When you use the inhaler for the first time, it may not deliver the right amount of medicine with the first puff. Before using this medicine, test or prime it. Hold the inhaler so that the white cover points up, then twist the cover and lift it off. Hold the inhaler upright (mouthpiece up) using the brown grip, then twist the middle of the inhaler fully in one direction as far as it will go, and then back again in the other direction. You will hear a click. Repeat this process one more time. You do not have to prime it again after this, even if you have not used it for a long time. After the inhaler is primed, twist the cover and lift it off. To load a dose, hold the inhaler in the upright position, then twist the grip fully in one direction as far as it will go, and then fully back again in the other direction. You will hear a click. Turn your head away from the inhaler and breathe out. Do not shake the inhaler. Place the mouthpiece between your lips and breathe in deeply and forcefully. You may not taste or feel the medicine. Do not chew or bite on the mouthpiece. Remove the inhaler from your mouth and breathe out. Do not blow or breathe into the inhaler. Repeat these steps if more than one dose is needed. When you are finished, place the cover back on the inhaler and twist shut. Rinse your mouth with water and spit out the water. Do not swallow the water. This helps prevent hoarseness, throat irritation, and infections in the mouth. Do not use the inhaler if it has been damaged or if the mouthpiece has become detached. Do not use a spacer with the Pulmicort Flexhaler™. Keep the inhaler clean and dry at all times. Follow the patient directions for cleaning and storing the inhaler. The inhaler has a dose indicator that keeps track of how many times you can use the inhaler before you need to open a new one. Check the dose indicator just below the mouthpiece. The dose indicator usually starts with either the number 60 or 120 when full. Discard the whole device when all doses have been used. The inhaler is empty when the number zero appears in the middle of the dose indicator window. You will be given a new inhaler each time you refill your prescription.

When using the Pulmicort Respules® liquid:

This medicine comes as a liquid that you breathe into the lungs with a special breathing machine called a jet nebulizer. The nebulizer has a face mask or mouthpiece. It is used by children who are 12 months to 8 years of age. Your doctor will tell you which type of nebulizer to use with this medicine and will show you how to use the nebulizer. The medicine and nebulizer come with patient instructions. Read the instructions carefully before using the medicine or the machine. If you or your child do not understand the instructions or are not sure how to use the nebulizer, check with your doctor. Use this medicine at the same time each day, unless your child's doctor tells you otherwise. Do not mix this liquid with other medicines. Open the sealed aluminum foil envelope containing the medicine. Remove one container from the strip of five plastic containers with sealed caps. Write the current date on the back of the envelope when you open the foil pouch. Each container has one dose of medicine. Place the unused containers back in the foil pouch. This will protect the medicine from light. Shake the container in a circular motion before using it. Hold the container upright and open it by twisting off the cap. Slowly squeeze out all of the contents of the container into the nebulizer cup. Throw the empty container away. If your child is using a face mask, make sure that the mask fits tightly on the face to avoid getting the medicine in the eyes. Turn on the compressor to begin nebulizing the medication. The nebulizer turns the medicine into a fine mist that the child breathes into the lungs using the mouthpiece or mask. After the dose is completed, wash your child's face to prevent skin irritation. Rinsing your child's mouth with water after each dose may help prevent hoarseness, throat irritation, and infections in the mouth. Do not allow your child to swallow the water after rinsing.

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 preventing an asthma attack: For inhalation dosage form (powder inhaler): Adults and children 6 years of age and older—At first, one or two puffs two times a day. Your doctor may increase your dose as needed. Children younger than 6 years of age—Use and dose must be determined by your doctor. For inhalation dosage form (suspension in a nebulizer): Children 12 months to 8 years of age—0.5 to 1 milligram (mg) in a nebulizer once a day, or divided and given twice a day. Each container of liquid has one dose and a new container is used for each dose. Infants younger than 12 months of age—Use and dose must be determined by your doctor.

Overdose

If you overdose Budenase and you don't feel good you should visit your doctor or health care provider immediately. Symptoms of overdose: thinning skin, easy bruising, changes in the shape or location of body fat (especially in your face, neck, back, and waist), increased acne or facial hair, menstrual problems, impotence, or loss of interest in sex.

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.

After you prime the bottle, there will only be 120 doses or sprays. Keep track of the number of sprays you use. Throw the bottle away after you use 120 sprays even if some liquid remains in the bottle.

Detailed Budenase dosage information

Side effects

The most common side effects associated with Budenase 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

In deciding to use a medicine, the risks of taking the medicine must be weighed against the good it will do. This is a decision you and your doctor will make. For this medicine, the following should be considered:

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Interaction between constitutively expressed heat shock protein, Hsc 70, and cysteine string protein is important for cortical granule exocytosis in Xenopus oocytes. In all three cases diagnosis was made based on persistent hematuria accompanied by prolonged fever of unclear origin and was subsequently confirmed by the presence of staphylococcus in the blood. Although the prognosis remains poor, there has been recent progress in the treatment of these tumors. This study was designed to define the relation of these excision volumes to the likelihood of microscopically detectable, residual disease based on tumor size, margin status, patient age, and histology. lpt6, a gene required for addition of phosphoethanolamine to inner-core lipopolysaccharide of Neisseria meningitidis and Haemophilus influenzae. We compared two different surgical approaches, standard microsurgical anterior temporal resection (ATL) and stereotactic radiofrequency amygdalohippocampectomy (SAHE) for MTLE, with respect to the extent of resection or destruction, clinical outcomes, and complications. Digital images taken of the lung tissue after processing and staining of the lung sections were examined by the PCM under light microscopy. Subcortical aphasia and neglect in acute stroke: the role of cortical hypoperfusion.

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An epidemiological survey of Theileria infections in small ruminants in central China. To elaborate on the involvement of the nigrostriatal and mesolimbic dopamine (DA) systems in modulating behavioral sensitization, locomotor activity and the time spent engaged in repetitive stereotyped behaviors following systemic amphetamine injection were assessed after electrical stimulation of the nucleus accumbens and neostriatum. The aim of this study was to determine the prevalence, type, and potential clinical outcome of errors in preparation and administration of insulin in resource-restricted setting hospitals. Death, hip fractures, ADL disability, and hospitalizations were ascertained during an average of 5.9 years of follow-up. Meta-analysis: obesity and the risk for gastroesophageal reflux disease and its complications. It was demonstrated that the cationic polymers could act as both an electrostatic and steric stabilizer to facilitate particle size reduction. Lactate elimination and O 2 consumption of the liver in narcotized dogs. Future research should focus on (1) the dose-dependent relationship between viremic exposure and the subsequent infectiousness of key mosquito species, (2) evaluation of vertebrate host competence for RVFV among North American mammal species, with particular emphasis on the order Artiodactyla, and (3) identification of areas with a high risk for RVFV introduction so data on local vector and host populations can help generate geographically appropriate amplification fraction estimates. Awareness amongst clinicians may render better health care delivery to subjects with alcohol dependence. The presence of insect prey was mimicked by placing the chemical inducers gelatine, salicylic acid and crustacean chitin on leaves.

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This study investigated the feasibility of using patient own fibrin isolated from whole blood to construct a new human cartilage, skin and bone. Dietary cholesterol fails to stimulate the human cholesterol 7alpha-hydroxylase gene (CYP7A1) in transgenic mice. Future applications may include targeted diaphragm injections with gene replacement therapy in neuromuscular diseases. Differential diagnosis of acute food poisoning and acute surgical conditions of the abdomen. Mothers of 30 infants who had experienced an emergency apnea episode and were placed on a home apnea monitor were studied longitudinally, using measures of mood disturbance (anxiety, depression, hostility, fatigue, vigor and confusion). Linear regression models were used to analyze the association between religiosity, as measured by affiliation, attendance, and having a clergy confidant, and logged values of C-reactive protein (CRP) concentration (mg/L). In a clinical sample of combat veterans, the LEC was significantly correlated, in the predicted directions, with measures of psychological distress and was strongly associated with PTSD symptoms.

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In follow-up lowering of the visual acuity, progression of visual field as well as electroretinographic changes occurred. Psychological and physiological origins of racism and other social discrimination. Effect of bear bile powder on STAT3 pathway in hepatocellular carcinoma xenograft. The results are discussed with respect to biomechanical adaptation strategies that deal with the consequences of increased noise in the neuromotor system due to enhanced mental processing. In addition, size, electrophoretic mobility, phase transition temperature, elasticity and membrane fluidity were measured before and after encapsulation. While an increasingly detailed picture about the control of cell proliferation is emerging, our knowledge about the control of cell expansion remains more limited. Bond strengths of the sodium salt of ethylenediamine-tetraacetic acid (Na2EDTA adjusted to pH 7.4) and glutaraldehyde-treated dentin cemented to composite resin with dilute solutions of the oligomers and then stored in water were determined by the procedure of Kemper and Kilian (1975).

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The title, Stay the Course, refers to the fact the system plans to stay afloat after four consecutive years of operational losses. Patients with gastroesophageal reflux (GER) present to the head and neck specialist with a myriad of nonspecific complaints that may be manifestations of pharyngoesophageal or upper airway involvement. Symptomatic severity of PRIME-MD diagnosed episodes of panic and generalized anxiety disorder in primary care. In medicated patients later VEP components showed enhancement over the right hemisphere as a function of the overall dose (chlorpromazine equivalent) of neuroleptics. Malaria in the triple border region between Brazil, Colombia and Peru. Suicide data, differentiated by month of suicide, sex, and method of suicide (violent vs nonviolent methods), were provided by Statistics Austria. To evaluate the effects of a dexmedetomidine constant rate infusion (CRI) and atropine on changes in global perfusion variables induced by hemorrhage and volume replacement (VR) in isoflurane-anesthetized dogs. It may be possible to reduce the frustrations inherent in the distance between the reviewer and the participants in the primary research by using full project reports rather than published articles. Dimerization of beta-site beta-amyloid precursor protein-cleaving enzyme. We investigate the accuracy and performance of the regularized version of the single-relaxation-time lattice Boltzmann equation for the case of two- and three-dimensional lid-driven cavities.

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