Medication info
Bepom Extended Release Tablet (Bepotastine Besylate)

Bepom Extended Release Tablet (Bepotastine Besylate)

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

MFDS item code 202204556 · Approved 2022.12.21 · Insurance code 622804920

Summary

Main use
Relief of perennial allergic rhinitis, pruritus associated with skin conditions, and chronic urticaria
Who takes it
Adults
Adult dose
Adults: Take 1 tablet once daily after a meal.

Ingredients

Manufacturer
Mothers Pharmaceutical Co., Ltd.

Efficacy & effects

Relief of perennial allergic rhinitis, pruritus associated with skin conditions, and chronic urticaria

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

This medication is used to treat perennial allergic rhinitis, chronic urticaria, and itching associated with skin diseases such as eczema or dermatitis.

How to take

Adult dose

Adults: Take 1 tablet once daily after a meal.

Precautions

This medication should not be used by individuals who have allergic reactions to its components. Additionally, this medication contains lactose, so individuals with a genetic issue that prevents the digestion of lactose should not take it. Patients with impaired kidney or liver function should be especially cautious when using this medication, and elderly individuals may also need to use it carefully due to potential declines in bodily function. This medication may cause neurological symptoms such as drowsiness, headache, and dizziness, as well as gastrointestinal symptoms such as dry mouth, indigestion, and diarrhea. There is also a chance of allergic reactions such as skin rash or swelling, so if any unusual symptoms occur, consult a doctor immediately. It is advisable to avoid driving or operating hazardous machinery while taking this medication. If a patient transitioning from long-term steroid treatment takes this medication, the reduction of the steroid dosage should be done gradually. Patients with weak kidney function may experience increased blood concentration of this medication, so treatment should start with lower doses and patient's condition must be closely observed. For patients with seasonal allergic rhinitis, it is best to start and stop this medication at appropriate times according to the season. If no effects are observed, it is preferable not to continue taking the medication for an extended period. Concomitant use with other antihistamines or alcohol should be avoided. Pregnant women or women who may become pregnant should not take this medication unless necessary, and should consult a doctor before making a careful decision. Nursing women should also avoid taking this medication as it can affect the baby through breast milk; if possible, breastfeeding should be stopped or the medication should be avoided. It is not recommended for children, as its safety has not been sufficiently confirmed. Elderly patients should take care, as decreased kidney function may cause the medication to remain in the body for extended periods. This medication may affect allergy test results, so it is advisable to stop taking it before undergoing testing. Finally, this medication should be stored out of reach of children and should not be transferred to other containers for safety and quality maintenance.

Side effects

  • Drowsiness
  • lethargy
  • headache
  • feeling of heaviness in the head
  • dizziness
  • thirst
  • dry mouth
  • glossitis
  • nausea
  • vomiting
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  • abdominal pain
  • discomfort in the upper abdomen
  • diarrhea
  • changes in white blood cell count
  • eosinophilia
  • elevated AST
  • elevated ALT
  • elevated r-GTP
  • elevated LDH
  • elevated total bilirubin
  • urine protein
  • urine glucose
  • urine hematuria
  • urine urobilinogen
  • rash
  • allergic reaction of swelling
  • nasopharyngitis
  • upper abdominal pain
  • increased blood 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 may be sensitive to air and moisture, so it should be stored in a tightly sealed container. The storage temperature should be maintained between 1°C to 30°C. Doing so will help maintain the medication's effectiveness for a longer period.

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.