Indications & Dose:
Gram-negative infections resistant to other antibacterials, including those caused by Pseudomonas aeruginosa, Acinetobacter baumanii and Klebsiella pneumoniae
Adult (body-weight up to 60 kg): 50 000–75 000 units/kg daily in 3 divided doses, to be administered into a totally implantable venous access device when giving via slow intravenous injection
Adult (body-weight 60 kg and above): 1–2 million units every 8 hours, to be administered into a totally implantable venous access device when giving via slow intravenous injection; maximum 6 million units per day
Adjunct to standard antibacterial therapy for Pseudomonas aeruginosa infection in cystic fibrosis
Adult: 1–2 million units twice daily, adjusted according to response, increased to 2 million units 3 times daily for subsequent respiratory isolates of Pseudomonas aeruginosa
Contraindications:
Myasthenia gravis
Side Effects:
Common or very common
When used by inhalation Bronchospasm . cough . dysphonia . nausea . sore mouth . Sore throat . taste disturbances . vomiting Uncommon
When used by inhalation Hypersalivation . thirst Rare
With intravenous use Vasomotor instability
Frequency not known
With intravenous use Apnoea . confusion . headache . muscle weakness . nephrotoxicity . neurotoxicity reported especially with excessive doses . perioral paraesthesia . peripheral paraesthesia . psychosis . rash . slurred speech . vertigo . visual disturbances
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