Azeclutine Tablet (Azelastine Hydrochloride)

Adult dose

As Azelastine Hydrochloride, administer 1 mg orally twice daily after breakfast and before bedtime; for bronchial asthma, 2 mg may be taken once. Adjust dosage appropriately according to age and symptoms.

This medication should not be used in children under 6 years of age. This medication contains lactose; therefore, individuals with genetic issues such as galactose intolerance, lactase deficiency, or glucose-galactose malabsorption should avoid it. Taking this medication may cause drowsiness; therefore, it is advised to refrain from driving or operating hazardous machinery. It may affect the central nervous system, causing symptoms such as drowsiness, lethargy, numbness in the hands and feet, and unsteadiness. Possible gastrointestinal effects include dry mouth, nausea, vomiting, decreased appetite, abdominal pain, constipation, and diarrhea. Occasionally, symptoms such as flushing of the face or difficulty breathing may occur. Respiratory effects may include nasal dryness. It may affect liver function and could lead to elevated liver enzyme levels. If there are skin rash-like hypersensitivity reactions, the medication should be discontinued immediately. Discomfort or hematuria, dysuria, and increased frequency of urination may occur. Blood-related issues may cause an increase in white blood cell count. Other side effects such as swelling or menstrual irregularities may also occur. Patients undergoing long-term steroid treatment should carefully manage the process of reducing steroid dosage when using this medication. Asthma patients should understand that this medication is not intended for immediate relief of sudden attacks. Seasonal allergy patients are advised to start this medication before symptoms worsen and continue taking it until symptoms subside. Alcohol consumption may enhance the sedative effects of this medication, so avoiding alcohol is recommended. Caution is necessary when taking it in conjunction with other medications, such as cimetidine. Women who are pregnant or may become pregnant should carefully consider the risks and benefits of taking this medication. Breastfeeding women should preferably avoid this medication as it can be transmitted through breast milk; if unavoidable, breastfeeding should be discontinued. The safety for premature infants, newborns, infants, and toddlers has not been established, thus caution is required in their use. Elderly individuals may have decreased physical function, so dosage adjustments should be made accordingly. This medication may taste bitter, which should be noted during administration. Keep out of reach of children, store in a cool, dry place away from direct sunlight. Do not transfer the medication to another container; it should be stored in its original packaging to prevent misuse and maintain quality.

Serious side effects

• Shortness of breath
• increased transaminase activity
• elevated AST
• ALT
• Al-P levels

Mild side effects

• Drowsiness
• lethargy
• numbness in limbs
• unsteadiness
• dry mouth
• nausea
• vomiting
• cough in the mouth
• decreased appetite
• abdominal pain

This medication should be stored in a tightly closed container that blocks light, at room temperature between 1 to 30 degrees Celsius. Storing it this way helps maintain the medication's effectiveness and prevents deterioration.

Appearance

Bright yellow round film-coated tablet

Package unit

30 tablets/bottle, 600 tablets/bottle