Medication info
Ajes  (Azelastine Hydrochloride)

Ajes (Azelastine Hydrochloride)

Prescription medicationTablet경구
Ingredient · strength
Azelastine Hydrochloride›1mg / 1 tablet
Manufacturer / importer
영일제약(주)
Appearance
Bright yellow round film-coated tablet
Packaging
30 tablets/bottle, 300 tablets/bottle
Approval status
Active

MFDS item code 200402287 · Notified 2004.12.17 · Insurance code 649401470

Summary

Main use
Improvement of respiratory and skin diseases such as bronchial asthma and allergic rhinitis
Who takes it
Adults
Adult dose
As Azelastine Hydrochloride, administer 1 mg orally, and in cases of bronchial asthma, 2 mg orally twice a day after breakfast and before bedtime. Adjust according to age and symptoms.

Ingredients

Manufacturer
영일제약(주)

Efficacy & effects

Improvement of respiratory and skin diseases such as bronchial asthma and allergic rhinitis

  • Bronchial asthma
  • allergic rhinitis
  • urticaria
  • eczema
  • dermatitis
  • atopic dermatitis
  • skin pruritus
  • itching
View approved original text

This medication is used for allergic and inflammatory diseases such as bronchial asthma, allergic rhinitis, urticaria, and atopic dermatitis.

How to take

Adult dose

As Azelastine Hydrochloride, administer 1 mg orally, and in cases of bronchial asthma, 2 mg orally twice a day after breakfast and before bedtime. Adjust according to age and symptoms.

Precautions

This medication should not be used in children under 6 years of age. This medication contains lactose, and it should not be administered to patients with genetic disorders that inhibit the digestion of lactose. This medication contains specific colorants, Yellow No. 4 and Yellow No. 5, so patients who are allergic or have experienced hypersensitivity reactions to these components should use it with caution. Drowsiness may occur when taking this medication, so it is safer to avoid driving or operating dangerous machinery. It may affect the central nervous system and may cause symptoms such as drowsiness, lethargy, tingling in the limbs, and unsteadiness. It may impact the gastrointestinal tract and can cause dry mouth, nausea, vomiting, loss of appetite, abdominal pain, constipation, and diarrhea. Although rare, symptoms such as flushing or shortness of breath may occur, so caution is required. Nasal dryness symptoms may appear, and there may be a rise in liver function test values. If hypersensitivity reactions such as skin rashes occur, discontinue the medication immediately. Urinary symptoms such as difficulty in urination, hematuria, and frequent urination may occur rarely. Rarely, an increase in white blood cells, edema, or menstrual irregularities have been reported. When patients undergoing long-term steroid treatment use this medication, careful management is required when reducing steroid doses. Patients with bronchial asthma should understand that this medication is not intended to quickly relieve an already occurring attack. Patients with seasonal allergies are advised to start taking it before symptoms worsen and to continue taking it during the symptom duration. Alcohol may enhance the drowsiness effect of this medication, so it is safer to avoid alcohol. Cimetidine can interact with this medication, so caution is advised when used together. Women who are pregnant or may become pregnant should only use this medication after carefully considering its benefits and risks, and nursing mothers should avoid it if possible or stop breastfeeding. This medication is not recommended for infants, newborns, or premature babies as its safety has not been adequately established for this age group. Elderly patients may have reduced physical function, so caution is required when using this medication, including reducing the dosage. The medication may have a bitter taste, so please be aware of this.

Side effects and when to seek care immediately

Serious side effects

Severe swelling (edema), difficulty breathing, rash (possible severe allergic reaction).

Mild side effects

  • Drowsiness
  • lethargy
  • limb paralysis
  • unsteadiness
  • dry mouth
  • nausea
  • vomiting
  • cough in the mouth
  • loss of appetite
  • abdominal pain
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  • constipation
  • diarrhea
  • discomfort in the upper abdomen
  • flushing of the face
  • shortness of breath
  • nasal dryness
  • elevated transaminase activity
  • increased AST
  • ALT
  • and Al-P
  • rash
  • urinary difficulties
  • hematuria
  • frequent urination
  • increased white blood cells
  • edema
  • menstrual irregularities.

Not everyone experiences these, and they can vary from person to person.

Storage

This medication is sensitive to light and should be stored in a lightproof, tightly closed container. The storage temperature should be maintained between 1 to 30 degrees Celsius, ideally at room temperature. By following this storage method, the medication's efficacy and safety can be well maintained.

Appearance and packaging

Appearance

Bright yellow round film-coated tablet

Package unit

30 tablets/bottle, 300 tablets/bottle

Same-ingredient medicines

Even with the same ingredient, strength, dosage form and how it is taken can differ.

Even with the same ingredient, the dose and directions can differ by strength and dosage form. Talk to a doctor or pharmacist before switching from a medication you are already taking.

Questions about this medicine

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For anything that needs medical judgment, consult a doctor or pharmacist.

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This drug information is based on data provided by the Korea Ministry of Food and Drug Safety.
Consult a doctor or pharmacist for accurate dosage, administration, and usage instructions.