To be reconstituted with sterile water for injection
Colour
Yellow to orange powder
Warnings and Precautions
Not to be used in pregnancy and children under 8 years unless clearly needed
Expiry
Check package for expiry date
Shelf Life
24 months from date of manufacture
Therapeutic Class
Glycylcycline antibiotics
Tigestat Tigecycline Injection Trade Information
Supply Ability
1000 Per Day
Delivery Time
7 Days
Sample Available
No
Sample Policy
Contact us for information regarding our sample policy
About Tigestat Tigecycline Injection
Dose Strength
50 mg
Composition
Tigecycline
Treatment
Used To Treat Serious Infections Such As Complicated Infection Of The Skin And Soft Tissues
Prescription/Non prescription
Prescription
Shelf Life
24 Months
Form
Injection
Product Packaging Type
Box
Product Brand
Tigestat
Minimum Order Quantity
100 Box
For IV Infusion Only
Schedule H Prescription Drug-caution
Not to be sold by retail without the prescription of a Registered Medical Practitioner
Each vial contains:
Tigecycline I.P. 50mg
Lactose I.P.
Dose: As directed by the Physician.
Store below 30C., protected from light and moisture.
Reconstitute with 5ml 0.9% w/v Sodium Chloride Injection, the resulting solution will contain 10mg/ml Tigecycline.
Reconstituted solution will be yellow to orange in colour, if not, the solution should be discarded.
Precise Treatment for Complicated Infections
Tigestat Tigecycline Injection is specifically recommended for adults facing severe and complicated skin or intra-abdominal infections. As a potent glycylcycline antibiotic, it effectively targets a wide spectrum of bacteria that may not respond to other medications. The carefully regulated dosage ensures optimal results under medical supervision, while its formulation allows for flexible hospital or clinical use.
Safe Handling and Storage Instructions
To maintain the effectiveness of Tigestat Tigecycline Injection, it is crucial to store the vial below 25C and protect it from light. The lyophilized powder must be reconstituted with sterile water for injection just prior to administration. Adherence to storage guidelines and checking the expiry date on the packaging help guarantee drug potency and patient safety.
FAQ's of Tigestat Tigecycline Injection:
Q: How should Tigestat Tigecycline Injection be prepared and administered?
A: Tigestat Tigecycline Injection must first be reconstituted with sterile water for injection by a healthcare professional. Once dissolved, it is administered intravenously according to the physician's dosage instructions.
Q: What conditions is Tigestat Tigecycline Injection recommended for?
A: This injection is indicated for adults with complicated skin and intra-abdominal infections where other antibiotics may be ineffective.
Q: When is Tigestat Tigecycline Injection not recommended?
A: Tigestat should not be used in pregnant women or children under 8 years old unless clearly needed, due to potential risks. It is intended only for adults and must be used strictly as prescribed.
Q: Where should Tigestat vials be stored before use?
A: Store the vials below 25C, away from light, and always keep them in their original packaging until use. Do not use the vial past its expiry date.
Q: What is the process for using Tigestat Tigecycline Injection?
A: A healthcare provider will reconstitute the lyophilized powder with sterile water for injection before giving it to you intravenously. The dosage and duration of therapy are determined by your physician.
Q: What are the main benefits of Tigestat Tigecycline Injection for patients?
A: Tigestat offers broad-spectrum coverage against difficult-to-treat bacteria, making it highly beneficial for adults with severe, complicated infections resistant to other treatments.
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