GMP Pharmaceutical Drug Gentamicin Injection

Category:Active Pharmaceutical Ingredients
Product Name:GMP Pharmaceutical Drug Gentamicin Injection
CAS No.:NA
Standard:In-house Standards
Price(USD):Negotiable
Company:NINGBO VOICE BIOCHEMIC CO., LTD.

Basic Info
  • Grade: pharmaceutical grade

    Factory Location: Ningbo

    Main Sales Markets: orth America,Central/South America,Western Europe,Eastern Europe,Australasia,Eastern Europe,Australasia,Asia,Middle East,Africa

  • Sample Provided: no

    Therapeutic indications gentamicin is indicated in bacteraemia, urinary tract infections, chest infections, severe neonatal infections and other serious systemic infections due to susceptible organisms, in adults and children including neonates. Consideration should be given to official local guidance on the appropriate use of antibacterial agents. Dose and method of administration Adults: Systemic infections: if renal function is not impaired, 3-5 mg/kg/day in divided doses according to severity of infection, adjusting according to clinical response and body weight. Serious infections: if renal function is not impaired, 5mg/kg daily in divided doses at six or eight hourly intervals. The total daily dose may be subsequently increased or decreased as clinically indicated. Urinary tract infections: as 'systemic infections'. Or, if renal function is not impaired, 160mg once daily may be used. Paediatric Patients: The daily dose recommended in children (aged 1 year and above) and adolescents with normal renal function, is 3-6 mg/kg body weight per day as 1 single dose (preferred) or up to 2 single doses. The daily dose in infants after the first month of life is 4.5-7.5 mg/kg body weight per day as 1 single dose (preferred) or up to 2 single doses. The daily dose in neonates is 4-7 mg/kg body weight per day. Due to the longer half-life, neonates are given the required daily dose in 1 single dose. Monitoring advice: Serum concentration monitoring of gentamicin is recommended, especially in elderly, in newborns and in patients with impaired renal function. Samples are taken at the end of a dosing interval (trough level). Trough levels should not exc
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