টাইফিম ভিআই

Live attenuate TY21a strain lacks enzyme UDP-4-galactose epimerase, which causes lipopolysaccharide to be synthesized under conditions that induce bacterial autolys; the avirulent strain produces enough lipopolysaccharide to evoke a protective immune response. Conveys active immunity via stimulation of production of endogenously produced antibodies

ব্যবহার

টাইফিম ভিআই is used for active immunization against typhoid fever for adults and children two years of age or older. Selective immunization with typhoid vaccine is recommended for the following:

Travellers to high endemic areas
Household contact of carriers
Healthcare personnel
Police, Armed forces and such other regimented personnel
Laboratory workers who work with Salmonella typhi

টাইফিম ভিআই এর দাম কত? টাইফিম ভিআই এর দাম

Typhim Vi in bangla
বাণিজ্যিক নাম	টাইফিম ভিআই
জেনেরিক	Typhoid Polysaccharide Vaccine
ধরণ	আইএম ইনজেকশন
পরিমাপ	25mcg/0.5ml, , +, 0025mg/05ml
দাম
চিকিৎসাগত শ্রেণি	Vaccines, Anti-sera & Immunoglobulin
উৎপাদনকারী	Sanofi Pasteur
উপলভ্য দেশ	Bangladesh, Australia, Canada, United States, Indonesia, Portugal,
সর্বশেষ সম্পাদনা	September 19, 2023 at 7:00 am

খাওয়ার নিয়ম / ব্যবহারের নিয়ম

টাইফিম ভিআই খাওয়ার নিয়ম / ব্যবহারের নিয়ম

A single dose of 0.5 ml is recommended for both adults and children 2 years of age or older. Subjects who remain at risk of typhoid fever should be given a single booster dose of the vaccine with an interval of not more than 3 years.

টাইফিম ভিআই is for intramuscular injection only. Do not inject intravenously.

টাইফিম ভিআই should be given intramuscularly in the deltoid and children should be injected intramuscularly either in the deltoid or the vastus lateralis. It should not be injected into the gluteal areas where there may be a nerve trunk.

টাইফিম ভিআই injection should be administered with caution to subjects with thrombocytopenia or bleeding disorders since bleeding may occur following an intramuscular administration to these subjects. Following injection, firm pressure should be applied to the site (without rubbing) for at least two minutes.

Typhoid vaccine can be co-administered with other vaccines but should not be mixed with other vaccines or medicinal products in the same syringe.

পার্শ্বপ্রতিক্রিয়া

Most recepients of Typhoid vaccine experience some reactions upon vaccination. These are generally moderate and short in duration. They mainly consist of local reactions at the injection site (erythema, induration and tenderness). Systemic reactions (malaise, headache, diarrhea, vomiting, myalgia and elevated temperature) are reported less commonly. In very rare cases allergic type reactions (pruritus, rash, urticaria) may be observed.

সতর্কতা

Not for treatment of typhoid fever. Vaccination may not provide full proetction thus, travellers should be advised to take all necessary precautions to avoid contact or ingestion of potentially contaminated food or water sources.

IM admin: Caution when used in patients with a history of bleeding disorders, patients on anticoagulant treatment or severely immunocompromised patients.

Pregnancy: the effect of Typhoid vaccine on fetal development or reproduction capacity has not been evaluated. Typhoid vaccine should only be used during pregnancy when there is a high risk of infection.

Lactation: Not known if excreted in breast; use caution

মিথস্ক্রিয়া

Concurrent use with antibiotics or immunoglobulins may reduce the efficacy of typhoid vaccine. Mefloquine may increase the efficacy of typhoid vaccine. May reduce the diagnostic effect of tuberculin tests.

গর্ভাবস্থাকালীন ব্যবহার

Pregnancy: The effect of Typhoid vaccine on fetal development or reproduction capacity has not been evaluated. Typhoid vaccine should only be used during pregnancy when there is a high risk of infection.

Lactation: It is not known if Typhoid vaccine is excreted in human milk. It may be administered to nursing mothers only if clearly needed.

বৈপরীত্য

The vaccine protects against typhoid fever caused by Salmonella typhi. Protection is not conferred against paratyphoid fever or illness caused by non-invasive Salmonella. Typhoid vaccine should not be administered to subjects with known hypersensitivity to any component of the vaccine or to subjects having shown signs of hypersensitivity after previous Typhoid vaccine administration, or after any other vaccine containing Vi polysaccharide Salmonella typhi antigens.

It may be expected that in patients receiving immunosuppressive treatment or patients with immunodeficiency, an adequate response may not be achieved. The administration of Typhoid vaccine should be postponed in subjects suffering from acute severe febrile illness