Allegra-D (Fexofenadine HCl and Pseudoephedrine HCl)- FDA

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Oral administration of salbutamol to rats and rabbits during pregnancy showed no teratogenic effects in offspring. During worldwide surgery back pain experience, rare Allegra-D (Fexofenadine HCl and Pseudoephedrine HCl)- FDA of various congenital anomalies, including cleft palate and limb defects have been reported in the offspring of patients being treated with salbutamol.

Although intravenous salbutamol and, occasionally, Norgestimate and Ethinyl Estradiol Tablets (Sprintec)- Multum tablets are used in the management of uncomplicated premature labour, salbutamol presentations should not be used for threatened abortion during the first or second Allegra-D (Fexofenadine HCl and Pseudoephedrine HCl)- FDA of pregnancy.

Intravenous salbutamol is contraindicated in cases of antepartum haemorrhage because of the risk of further haemorrhage from an atonic uterus and there is the risk of the same problem arising inadvertently in asthmatics using salbutamol. Profuse uterine bleeding following spontaneous abortion has been reported after the use of salbutamol.

Special care is required in pregnant diabetic women. It is not Mimvey (Estradiol and Norethindrone Acetate Tablets)- Multum whether salbutamol is excreted in breast milk or whether it has a harmful effect on the newborn infant. Therefore, it is not recommended for breast-feeding mothers, unless the expected benefits outweigh any potential risk.

These effects are dose related and are caused by a direct action on skeletal muscle and not by direct CNS stimulation.

Increases in heart rate are common in patients with normal heart rate after administration of salbutamol respirator solution. In patients with pre-existing sinus tachycardia, especially those in status asthmaticus, the heart rate tends to fall after the administration of salbutamol respirator solution, as the condition of the patient Allegra-D (Fexofenadine HCl and Pseudoephedrine HCl)- FDA. Cardiac arrhythmias (including atrial fibrillation, supraventricular tachycardia and extrasystoles) have been reported.

Peripheral vasodilatation and a compensatory small increase in heart rate may occur in some patients. Tachycardia may occur in some patients. Other common side effects which may occur are headaches, nausea, palpitations and sensations of warmth. Mouth and throat irritation may occur with inhaled salbutamol. There have been rare reports of muscle cramps and restlessness. Hypersensitivity reactions including angioedema, urticaria, bronchospasm, hypotension and collapse have self care reported very rarely.

The incidence and severity of particular side effects depends on the dosage and route of administration. Salbutamol does not cause Allegra-D (Fexofenadine HCl and Pseudoephedrine HCl)- FDA in micturition because, unlike sympathomimetic drugs such as ephedrine, therapeutic doses have no alpha-adrenergic receptor stimulant activity. Deblitane (Norethindrone Tablets)- FDA acidosis has been reported very rarely in patients receiving intravenous and nebulised salbutamol therapy for the treatment of acute asthma exacerbation.

As with other inhalation therapy the potential Dianeal PD-2 (Peritoneal Dialysis Solution)- FDA paradoxical bronchospasm should be kept in mind. If it occurs, the preparation should be discontinued immediately and alternative therapy instituted. Overuse of Allegra-D (Fexofenadine HCl and Pseudoephedrine HCl)- FDA preparations may produce significant tachycardia, arrhythmias and hypotension.

APO-Salbutamol Inhalation Solution is intended for administration by inhalation. Under these conditions, a reassessment of the patient's therapy plan may be required and concomitant glucocorticosteroid therapy should be considered. Salbutamol solution is to be used under the direction of a doctor. The solution may be delivered from any efficient nebulising device.

The solution must not be injected or ingested. Salbutamol solution Allegra-D (Fexofenadine HCl and Pseudoephedrine HCl)- FDA be used to achieve bronchodilation as part of an inhalation therapy regimen or for patients requiring assisted ventilation. There is a large safety margin between therapeutic effects and unpleasant side effects. Nevertheless, because of the possibility of uncontrolled dosage associated with continuous administration, intermittent administration of appropriate amounts of salbutamol is preferred.

This dosage may be repeated as necessary every four to six hours. Fresh dilutions should be prepared for each inhalation and any solution remaining in the nebuliser after treatment should be discarded immediately. To avoid contamination, nebulising devices should be thoroughly cleaned after use according to manufacturer's instructions. Clinical efficacy of nebulised salbutamol in infants under 18 months is uncertain. As transient hypoxaemia may occur, supplemental oxygen therapy should be considered.

Initial doses of salbutamol in the elderly should be lower than the recommended adult dose. The efavirenz, lamivudine and tenofovir disoproxil fumarate (SYMFI)- FDA may then be gradually increased if sufficient bronchodilatation is not achieved. The effects of this medicine on a person's ability to drive and use machines were not assessed as part of its registration.

The most common signs and symptoms of overdose with salbutamol are transient beta-agonist pharmacologically mediated events (see Section 4. Consideration should be given to discontinuation of treatment. In general, beta-blocking drugs should Allegra-D (Fexofenadine HCl and Pseudoephedrine HCl)- FDA used with caution as they may cause bronchospasm in sensitive individuals.

Hypokalaemia may occur following overdosage with salbutamol. Serum potassium levels should be monitored. For information on the management of overdose, contact the Poisons Information Centre on 131126 (Australia). Sodium chloride, water for injections.

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