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        Each film coated Boostim LB SR tablet contains:
        Amoxicillin Trihydrate IP equivalent to Amoxicillin 1000 mg, Clavulanate Potassium USP equivalent to Clavulanic Acid 62.5mg,Lactic Acid Bacillus 60 million spores(Appropriate overages of Lactic Acid Bacillus spores added)
        Therapeutic Indications & Usage
        Boostim LB SR is indicated for treatment of :
        Acute bacterial sinusitis
Acute exacerbation of chronic bronchitis
Community acquired pneumonia
Urinary tract infections.
        Boostim LB SR is effective in treatment of penicillin resistant S.pneumoniae, additional activity against beta lactamase producers, H.influenzae & M.catarrhalis.
  • BOOSTIM LB-SR is not advocated for those with a history of hypersensitivity to beta-lactams, e.g. penicillins & cephalosporins.
  • BOOSTIM LB-SR is also contraindicated in those with previous history of amoxicillin-clavulanic acid-associated jaundice / hepatic dysfunction.
  • BOOSTIM LB-SR should be avoided if infectious mononucleosis is suspected since the occurrence of a morbilliform rash has been associated with this condition following the use of amoxicillin.
  • BOOSTIM LB-SR should not be used in renal failure when glomerular filtration rate is less than 30 ml/minute.
        Precautions & Warnings
        BOOSTIM LB-SR should be advocated with caution in presence of hepatic dysfunction or renal impairment.
        Since BOOSTIM LB-SR contains amoxicillin, an aminopenicillin, it is not the treatment of choice in patients presenting with sore throat or pharyngitis because of the possibility that the underlying cause is infectious mononucleosis, in the presence of which there is a high incidence of rash if amoxicillin is used.
        BOOSTIM LB-SR is not ideally meant for pregnant lady or lactating mother; however, it could be advocated only if strictly necessary.
        Adverse Reactions
        The most frequently reported adverse effects with amoxicillin (BOOSTIM LB-SR) are indigestion, diarrhea, nausea, vomiting, abdominal pain, skin rashes, urticaria and erythema multiforme, vaginitis, oral thrush, abnormal taste, headache, dizziness, tiredness and hot flushes.
        Other side effects attributable to amoxicillin (in BOOSTIM LB-SR) include hypersensitivity reactions, other gastrointestinal reactions including superficial tooth discoloration, hepatitis, cholestatic jaundice, hematologic changes & central nervous system effects including convulsions.
        Drug Interaction:
        Probenecid decreases the renal tubular secretion of amoxicillin.Concomitant use with BOOSTIM LB- SR may result in increased &prolonged blood levels of the combined administration of allopurinol & ampicillin substantially increases the incidence of skin rashes and BOOSTIM LB-SR must be cautiously coadministered with allupurinol
        Recommended Dosage & Administration
        In Acute bacterial sinusitis – 1 tablet BID for 10days
        In Acute exacerbation of chronic bronchitis-- 1 tablet BID for 7 days.
        In Community acquired pneumonia—1 tablet BID for 7-10 days.
        In Urinary tract infections.------- 1 BID for 7 days.
        BOOSTIM LB-SR 1g Tablets: Blisters of 10s


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