Kanamycin A Sulfate CAS:25389-94-0
Kanamycin A sulfate is typically administered through intramuscular or intravenous injection, depending on the type and severity of the infection being treated. The dosage and duration of treatment with kanamycin A sulfate 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 A sulfate, healthcare providers should perform appropriate testing to confirm the susceptibility of the infecting bacteria and ensure the effectiveness of the antibiotic. Patients must strictly adhere to the prescribed dosing schedule and complete the full course of treatment to prevent the development of antibiotic resistance and ensure eradication of the infection. Monitoring for potential side effects, such as nephrotoxicity and ototoxicity, is crucial during treatment with kanamycin A sulfate. Regular assessments of kidney function and hearing may be necessary to detect any adverse reactions promptly. Proper storage of kanamycin A sulfate following the manufacturer's guidelines, safe handling practices, and the correct disposal of unused medication are essential to maintain the drug's stability and prevent antimicrobial resistance. Seeking guidance from a healthcare professional on the use of kanamycin A sulfate is key to achieving optimal therapeutic outcomes and minimizing the risk of complications.
Composition | C18H38N4O15S |
Assay | 99% |
Appearance | white powder |
CAS No. | 25389-94-0 |
Packing | Small and bulk |
Shelf Life | 2 years |
Storage | Store in cool and dry area |
Certification | ISO. |