Medication info
Univepotas Extended Release Tablet (Bepotastine Besilate)

Univepotas Extended Release Tablet (Bepotastine Besilate)

Prescription medicationTabletOral
Ingredient · strength
Bepotastine Besylate›12.22mg / 1 tablet
Manufacturer / importer
Korea Union Pharm Co., Ltd.
Appearance
White round film-coated tablet
Packaging
30 tablets/bottle, 300 tablets/bottle
Approval status
Active

MFDS item code 202204554 · Approved 2022.12.21 · Insurance code 665508470

Summary

Main use
Relief of allergic rhinitis, chronic urticaria, and itching associated with skin conditions (eczema, dermatitis, etc.)
Who takes it
Adults
Adult dose
Adults: Take 1 tablet once daily after a meal.

Ingredients

Manufacturer
Korea Union Pharm Co., Ltd.

Efficacy & effects

Relief of allergic rhinitis, chronic urticaria, and itching associated with skin conditions (eczema, dermatitis, etc.)

  • Perennial allergic rhinitis
  • chronic urticaria
  • pruritus
  • eczema
  • dermatitis
  • cutaneous pruritus
  • urticaria
View approved original text

This medication is used to effectively relieve itching associated with various skin diseases, including perennial allergic rhinitis and chronic urticaria, as well as eczema and dermatitis.

How to take

Adult dose

Adults: Take 1 tablet once daily after a meal.

Precautions

This medication should not be used in patients with hypersensitivity to the ingredients. Also, this medication contains lactose, so it should not be administered to patients with genetic issues such as galactose intolerance, Lapp lactase deficiency, or glucose-galactose malabsorption. Patients with renal or liver impairment, as well as the elderly, should use this medication with extra caution. During the use of this medication, side effects such as drowsiness, headache, dizziness, dry mouth, nausea, vomiting, abdominal pain, and diarrhea may occur, so caution is advised. Additionally, blood counts or liver function tests may change, so regular testing may be necessary. This medication may cause drowsiness; therefore, it is advisable to avoid driving a car or operating dangerous machinery while taking it. Patients who have been on long-term steroid treatment should gradually reduce their steroid dosage when taking this medication and require medical supervision. Patients with reduced kidney function may have increased blood concentrations of this medication; therefore, starting at a low dose and adjusting or pausing doses if adverse reactions occur is necessary. For patients with seasonal allergic rhinitis, it is recommended to start taking this medication before symptoms begin and continue during the symptom period. If no effects manifest, it is advisable not to take this medication for an extended period. This medication may have intensified side effects when taken with alcohol, so it should not be taken together. Women who are pregnant or may become pregnant are advised not to use this medication, and if it is deemed necessary, consultation with a doctor is essential. Nursing mothers are also recommended to avoid breastfeeding while taking this medication. Safety in children has not been established; thus, administration to children should be approached with caution. Elderly patients may have an increased risk of elevated drug concentrations due to diminished kidney function, thus requiring careful monitoring. This medication may affect allergy testing; hence, it is recommended to stop taking it before the tests. Finally, this medication should be kept out of reach of children, and it is advantageous for safety and quality to avoid transferring it to another container.

Side effects

  • Drowsiness
  • lethargy
  • headache
  • heaviness in the head
  • dizziness
  • dry mouth
  • dry oral mucosa
  • glossitis
  • nausea
  • vomiting
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  • stomach pain
  • upper abdominal discomfort
  • diarrhea
  • fluctuation in white blood cell count
  • eosinophilia
  • elevated AST
  • elevated ALT
  • elevated r-GTP
  • elevated LDH
  • elevated total bilirubin
  • urinary protein
  • urinary glucose
  • urinary hematuria
  • urinary urobilinogen
  • rash
  • hypersensitivity reaction with swelling
  • nasopharyngitis
  • upper abdominal pain
  • elevated serum bilirubin
  • detection of leukocytes in urine
  • lymphadenitis
  • cervical stenosis
  • nasal dryness
  • dyspepsia
  • hives
  • thirst
  • abdominal discomfort
  • facial swelling
  • elevated SGOT
  • elevated SGPT
  • palpitations
  • facial flushing
  • bitter taste
  • sensory impairment
  • contusion
  • tremor
  • constipation
  • folliculitis
  • peripheral edema
  • generalized edema
  • erythema
  • pruritus
  • frequent urination
  • peripheral coldness

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

Storage

This medication should be stored in a tightly sealed container to protect it from air or moisture. It is best stored at room temperature between 1 and 30 degrees Celsius.

Appearance and packaging

Appearance

White 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.