Bepozic Tablet Uses Dosage Side Effects Price Composition Precautions and Substitutes

Bepotastine Besilate Tablets 10 mg

1. NAME OF MEDICINAL PRODUCT
   Bepozic 10 mg Tablet
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5. COMPOSITION
   Each tablet contains :
   Bepotastine Besilate …. 10 mg
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7. USAGE/ INDICATIONS
   For the treatment of allergic rhinitis, itching associated with cutaneous disorder (eczema/dermatitis, prurigo, dermal pruritus) in adult patients.
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11. DOSAGE AND ADMINISTRATION
12. Bepotastine Besilate tablets should be orally administered to adults in a dose of 10 mg twice daily. The dosage might change depending on the age and symptoms.
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15. CONTRAINDICATIONS
    This drug should not be given to those who have history of hypersensitivity symptoms.
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17. WARNINGS AND PRECAUTIONS
    A ) Special warnings and precautions for use
    This drug must be used with caution for the following patients –
    • Patients with impaired liver functioning. Blood levels might reach higher levels after administration. Prescribe low dose initially and increase it gradually. Stop administration when any abnormality is detected.
    • Bepotastine must be used with caution for the patients on long term steroid hormone therapy. Always check the dosage when the dose of steroid is reduced for administration of Bepotastine
    • Start administration just before the onset of the symptomsin patients with seasonal symptoms and stop it whern the symptom ends.
    • Stop administration if the symptom persists even after starting Bepotastine Besilate treatment
    • Use with caution in the elderly since their physiological functions are declined in general and blood concentration may be higher.

B ) Interaction with other medicinal products and other forms of interaction
None.

C ) Fertility, pregnancy and lactation
a ) Avoid administration to pregnant women or women who might become pregnant. Incase of the necessity of administration to those above, administer only when therapeutic efficiency is greater than risk. (According to animal studies, it is found that the drug affects fetus).
b ) It is ideal not to administer to those who breast feed. In case of the necessity of administration to those above, breastfeeding should be avoided. (According to studies on rats, it is found that the drug is excreted in breast milk.)
c ) Administration to infants
The safety of administration to premature baby, newborn baby, infant and toddler has not been established.

7. UNDESIRABLE EFFECTS
   The most common reported adverse reactions are drowsiness, dry mouth, nausea, gastric pain, diarrhoea, stomach discomfort, malaise and vomiting. Other side effects are ALT (GPT) elevation, AST (GOT) elevation, y-GTP elevation, occult blood in urine.
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11. OVERDOSAGE
    None.
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13. INCOMPATIBILITIES
    Not Applicable
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15. SHELF LIFE
    24 Months from manufacture Date.
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17. PRICE – …………
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19. STORAGE AND HANDLING INSTRUCTIONS
    Store in dry, well ventilated place at temperature not exceeding 30°C.
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21. CAUTION
    Bepotastine may cause drowsiness. Avoid operating machines and driving after administration.
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23. PACKAGING INFORMATION
    Available in strip of 10 Tablets.

15. Manufactured by – Glenmark Pharmaceuticals
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Bepotastine besilate tablets 10mg for skin

Bepotastine besilate ( Bepozic 10mg tablet ) is used for skin itching associated with cutaneous disorder (eczema/dermatitis, prurigo, dermal pruritus) in adult patients.

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