Kanamycin base CAS:8063-07-8
Kanamycin base is typically administered through intramuscular or intravenous injection, depending on the type and severity of the infection being treated. The dosage and duration of kanamycin base treatment are determined based on factors such as the patient's age, weight, renal function, and the specific strain of bacteria causing the infection. Before using kanamycin base, healthcare providers should conduct appropriate testing to confirm the susceptibility of the infecting bacteria and ensure the antibiotic's effectiveness. Patients are advised to strictly adhere to the prescribed dosing regimen and complete the full course of treatment to prevent the development of antibiotic resistance and ensure successful eradication of the infection. Monitoring for potential side effects, such as nephrotoxicity and ototoxicity, is crucial during kanamycin base therapy. Regular assessments of kidney function and hearing may be necessary to promptly identify any adverse reactions. Proper storage of kanamycin base following manufacturer guidelines, safe handling practices, and the correct disposal of unused medication are vital to maintain drug stability and prevent antimicrobial resistance. Seeking guidance from a healthcare professional regarding kanamycin base use is essential for achieving optimal therapeutic outcomes and reducing the risk of complications.
Composition | C18H38N4O15S |
Assay | 99% |
Appearance | white powder |
CAS No. | 8063-07-8 |
Packing | Small and bulk |
Shelf Life | 2 years |
Storage | Store in cool and dry area |
Certification | ISO. |