Delamanid CAS:681492-22-8
Delamanid is a critical pharmacological tool in the management of multidrug-resistant tuberculosis, a severe form of tuberculosis that does not respond to standard first-line treatments. It is commonly included in combination therapy regimens for MDR-TB to improve treatment outcomes and reduce the risk of further drug resistance development. Healthcare providers prescribe delamanid alongside other second-line anti-tuberculosis medications based on individual patient factors, including the extent of drug resistance, previous treatment history, and overall health status. The medication is typically administered orally in tablet form, with dosing frequency and duration tailored to each patient's specific needs. Patients undergoing delamanid treatment are advised to adhere strictly to the prescribed regimen, as consistent medication intake is crucial for achieving therapeutic success and minimizing the risk of treatment failure. Regular monitoring for potential side effects, such as gastrointestinal disturbances or changes in liver function, is essential during the course of treatment. Delamanid therapy is usually initiated and supervised by healthcare professionals experienced in managing drug-resistant tuberculosis cases. Collaboration between the healthcare team and the patient is vital to ensure treatment compliance, monitor progress, and address any concerns or complications promptly. In conclusion, delamanid plays a significant role in combating multidrug-resistant tuberculosis, offering patients and healthcare providers an effective treatment option to combat this challenging infectious disease and prevent its further spread within communities.
Composition | C25H25F3N4O6 |
Assay | 99% |
Appearance | white powder |
CAS No. | 681492-22-8 |
Packing | Small and bulk |
Shelf Life | 2 years |
Storage | Store in cool and dry area |
Certification | ISO. |