Vancomycin VANCOGRAM Inj
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Indications lower respiratory tract infections septicemia bone infections sstis staphylococcal endocarditis. Dosage : adult dose : the usual adult dose is the equivalent of 500 mg of vancomycin every 6 hours or 1 g every 12 hours. Paediatric dose : 10 - 15 mgkg every 8 hours.
Estraheal Tablets
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Lavir 150mg Tablets
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VANCOMYCIN HYDROCHLORIDE INJECTION 500 / 1000 MG
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VANCOMYCIN HYDROCHLORIDE INJECTION 500 / 1000 MG tricyclic glycopeptide antibiotic Vancomycin Hydrochloride Injection 500 & 1000 mg is a tricyclic glycopeptide antibiotic derived from Amycolatopsis orientalis .Vancomycin is indicated for the treatment of serious or severe infections caused by susceptible strains of methicillin-resistant (beta-lactam-resistant) staphylococci. It is indicated for penicillin-allergic patients, for patients who cannot receive or who have failed to respond to other drugs, including the penicillins or cephalosporins .Vancomycin is indicated for initial therapy when methicillinresistant staphylococci are suspected, but after susceptibility data are available, therapy should be adjusted accordingly.Vancomycin is effective in the treatment of staphylococcal endocarditis. Its effectiveness has been documented in other infections due to staphylococci, including septicemia ,bone infections, lower respiratory tract infections, skin and skin structure infections. When staphylococcal infections are localized and purulent, antibiotics are used as adjuncts to appropriate surgical measures. India has many manufacturers who manufacture Vancomycin Hydrochloride Injection 500 & 1000 mg .To know more contact us. 3s corporation is Supplier,Exporter ,Wholesaler for Vancomycin Hydrochloride Injection 500 & 1000 mg in India. ADDITIONAL INFORMATION Rapid bolus administration (e.g., over several minutes) may be associated with exaggerated hypotension, including shock, and, rarely,cardiac arrest. Vancomycin should be administered over a period of not less than 60 minutes to avoid rapid-infusion-related reactions. Stopping the infusion usually results in prompt cessation of these reactions. SIDE EFFECTS INFUSION-RELATED EVENTS During or soon after rapid infusion of vancomycin, patients may develop anaphylactoid reactions, including hypotension, wheezing, dyspnea, urticaria. Rapid infusion may also cause flushing of the upper body NEPHROTOXICITY Renal failure, principally manifested by increased serum creatinine or BUN concentrations, especially in patients administered large doses of vancomycin, has been reported rarely. GASTROINTESTINAL Onset of pseudomembranous colitis symptoms may occur during or after antibiotic treatment . OTOTOXICITY A few dozen cases of hearing loss associated with vancomycin have been reported. Most of these patients had kidney dysfunction or a preexisting hearing loss or were receiving concomitant treatment with an ototoxic drug. PHLEBITIS Inflammation at the injection site has been reported.
Geftib Tablets
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Geftib Tablet is used for Treatment of metastatic non-small cell lung cancer in tumors with epidermal growth factor receptor exon 19 deletions or exon 21 substitution mutations and other conditions. Geftib Tablet may also be used for purposes not listed in this medication guide.Geftib Tablet contains Gefitinib as an active ingredient. Geftib Tablet works by blocking signalling of epidermal growth factor receptor dependent proliferation.Geftib Tablet – Side-effectsThe following is a list of possible side-effects that may occur from all constituting ingredients of Geftib Tablet. This is not a comprehensive list. These side-effects are possible, but do not always occur. Some of the side-effects may be rare but serious. Consult your doctor if you observe any of the following side-effects, especially if they do not go away. Skin reactions Nail disorders Diarrhea Vomiting Nausea Stomatitis Decreased appetite Conjunctivitis Blepharitis Dry eye Geftib Tablet – Precautions & How to UseBefore using Geftib Tablet, inform your doctor about your current list of medications, over the counter products (e.g. vitamins, herbal supplements, etc.), allergies, pre-existing diseases, and current health conditions (e.g. pregnancy, upcoming surgery, etc.). Some health conditions may make you more susceptible to the side-effects of the drug. Take as directed by your doctor or follow the direction printed on the product insert. Dosage is based on your condition. Tell your doctor if your condition persists or worsens. Important counseling points are listed below : Avoid concomitant use of this drug with proton pump inhibitors Contact doctor for new onset or worsening of pulmonary symptoms such as dyspnea, cough and fever Contact doctor for severe or persistent diarrhea Contact doctor if developping eye symptoms, lacrimation, light sensitivity, blurred vision, eye pain, red eye, or changes in vision Discontinue breast-feeding during treatment with this drug If treatment with a proton-pump inhibitor is required, take this drug 12 hours after the last dose or 12 hours before the next dose of the proton-pump inhibitor Monitor your liver function
Cefprozil
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