Alti-Orciprenaline
Name: Alti-Orciprenaline
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Uses For Alti-Orciprenaline
Metaproterenol is used to treat asthma and bronchospasm in patients with bronchitis, emphysema, and other lung diseases.
Metaproterenol belongs to the family of medicines known as adrenergic bronchodilators. Adrenergic bronchodilators are medicines that open up the bronchial tubes (air passages) in the lungs. They relieve cough, wheezing, shortness of breath, and troubled breathing by increasing the flow of air through the bronchial tubes.
This medicine is available only with your doctor's prescription.
Precautions While Using Alti-Orciprenaline
It is very important that your doctor check your progress or your child's progress at regular visits. This will allow your doctor to see if the medicine is working properly and to check for any unwanted effects.
Check with your doctor at once if you or your child continue to have breathing problems after using a dose of this medicine or if your condition gets worse.
Do not change your dose or stop using this medicine without asking your doctor first.
Do not take other medicines unless they have been discussed with your doctor. This includes prescription or nonprescription (over-the-counter [OTC]) medicines for appetite control, asthma, colds, cough, hay fever, or sinus problems, and herbal or vitamin supplements.
For Healthcare Professionals
Applies to metaproterenol: compounding powder, inhalation aerosol, inhalation aerosol with adapter, inhalation solution, oral syrup, oral tablet
General
Metaproterenol has been usually well-tolerated and adverse effects that occurred were consistent with its pharmacological activity. Additionally, partial or complete tolerance may develop to these side effects. In general, the severity of these effects are dependent on the dose and the route of administration. Metaproterenol given by metered dose inhaler (MDI) is associated with less systemic effects than administration of higher dosages orally or by nebulizer.[Ref]
Cardiovascular
Cardiovascular side effects have included palpitations and peripheral vasodilation, commonly resulting in reflex tachycardia. This may be caused by the interaction of metaproterenol with beta-1 and beta-2 receptors. Blood pressure may increase or decrease. Metaproterenol in higher dosages may rarely aggravate angina, myocardial ischemia, or cause atrial or ventricular arrhythmias.[Ref]
Musculoskeletal
Musculoskeletal side effects have included tremors. Tolerance often develop to the tremorogenic effects following prolonged use of this medication. Severe muscle cramping may occur infrequently.[Ref]
Metabolic
The hypokalemic effect is due to the stimulation of beta-2 receptors that are linked to sodium-potassium ATPase in skeletal muscles, resulting in an intracellular influx of potassium.[Ref]
Metabolic side effects have included hypokalemia, hypophosphatemia, hyperglycemia, and elevations in plasma insulin.[Ref]
Nervous system
Nervous system side effects have included restlessness, nervousness, anxiety, irritability, headache, dizziness, and insomnia.[Ref]
Other
Other side effects have included the development of tachyphylaxis to the bronchodilating effects of metaproterenol. Although conflicting data exist, complete clinical tolerance has not been observed.[Ref]
Hypersensitivity
A 25-year-old woman respiratory therapist with a history of an itchy dermatitis on the face, neck, and upper extremities showed a positive reaction to metaproterenol on skin patch testing.[Ref]
Hypersensitivity side effects have included rare reports of dermatitis.[Ref]
Respiratory
Respiratory side effects have included pulmonary edema in pregnant patients receiving the drug intravenously.[Ref]
Some side effects of metaproterenol may not be reported. Always consult your doctor or healthcare specialist for medical advice. You may also report side effects to the FDA.
Usual Adult Dose for Asthma - Maintenance
Oral: 20 mg 3 to 4 times a day.
Inhalation aerosol: 2 to 3 inhalations every 3 to 4 hours, up to 12 inhalations/day.
Inhalation solution: 10 to 15 mg (0.2 to 0.3 mL of 5% solution) every 4 to 6 hours.
Renal Dose Adjustments
Data not available
Liver Dose Adjustments
Data not available
Dialysis
Data not available
Metaproterenol Breastfeeding Warnings
There are no data on the excretion of metaproterenol into human milk. The manufacturer recommends that caution be used when administering metaproterenol to nursing women.
Metaproterenol Identification
Substance Name
Metaproterenol
CAS Registry Number
586-06-1
Drug Class
Anti-Asthmatic Agents
Bronchodilators
Beta Adrenergic Agonists