Influvax Tetra is suggested for adults and children aged six months and older, particularly those at high risk of related problems, such as youngsters, senior people, those who are vulnerable, and those living in influenza epidemic regions. The vaccination can allow the body to produce antibodies against the influenza virus and can be used to prevent illness caused by the virus.
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Influenza vaccinations, usually known as flu injections or flu jabs, are immunizations that protect against influenza virus infection. These vaccinations are usually considered safe. Vaccines are available in both inactive and weakened viral forms. Flu vaccination can help minimize flu-related symptoms, medical visits, and lost work and school, as well as avoid flu-related hospitalizations and fatalities.
Interaction with alcohol is unknown. Please consult your doctor.
Influvax Tetra is probably safe to use during pregnancy.
Animal studies have shown low or no adverse effects on the fetus. Please consult your doctor.
Influvax Tetra should be used with caution during lactation. Breastfeeding should be held until the treatment of the mother is completed and the drug is eliminated from her body.
Influvax Tetra does not usually affect your ability to drive.
There is limited information available on the use of this injection in patients with kidney disease. Please consult your doctor.
There is no data available. Please consult a doctor before consuming the drug.
Influvax Tetra is a group of substances that act to sensitize the natural immune system of the body towards the influenza virus so that if infected, the body’s immune system can neutralize the virus and prevent the development of influenza.
The influenza virus vaccine inactivated promotes immunity to the influenza virus by inducing specific antibody formation.
Adult Dose
Child Dose
The influenza vaccine is given yearly.
Intramuscular injection (IM) on the deltoid. This vaccine should be administered before the beginning of the influenza season or as required by the epidemiological situation. Vaccination should be repeated every year with an age-appropriate dose of vaccine of updated antigen composition.
Immunosuppressants, antineoplastics, or high doses of corticosteroids may reduce response to vaccines. Increased antibody response with aldesleukin and aspirin. May increase the anticoagulant effects of warfarin.
Annual vaccination against influenza with an age-appropriate formulation is recommended
Healthcare workers who care for immunocompromised people (ie, those who require care in a protected environment) should be given IIV or RIV4 rather than LAIV (or they should avoid contact with the immunocompromised people for 7 days after getting the vaccine).
Known anaphylactic hypersensitivity reactions to egg proteins (eggs or egg products), chicken proteins, or any other component of the vaccine including traces (formaldehyde, octoxinol 9 (Triton X-100), and neomycin). Immunization should not be performed during a febrile or acute illness.
A patient can suffer from the following side effects:
In children under 5 years of age, systemic reactions (e.g. fever, malaise, myalgia) may be more pronounced. Local Reactions: Erythema (redness), swelling, pain, ecchymosis, induration. Systemic Reactions: Fever, malaise, shivering, fatigue, headache, sweating, joint and muscular pain. These reactions usually disappear within 1-2 days without treatment. Rarely: Neuralgia, paresthesia, convulsions, and transient thrombocytopenia Allergic reactions leading to shock in rare cases. Vasculitis with transient renal involvement, in very rare cases.
Use in pregnancy: Safety of use during pregnancy has not been established; the benefits of vaccination should be weighed against potential risks. However, as an inactivated vaccine, it does not share the theoretical risks associated with live vaccines.
Since this vaccine contains traces of formaldehyde, octoxinol 9 (Triton X-100), and neomycin due to the use of these substances during production, it should be used with caution in subjects with a hypersensitivity to any of these substances. Patients with a history of Guillain-Barré Syndrome (GBS) with an onset related in time to influenza vaccination may be at increased risk of again developing GBS if given an influenza vaccine. Use in pregnancy & lactation: Safety of use during pregnancy has not been established; the benefits of vaccination should be weighed against potential risks. However, as an inactivated vaccine, it does not share the theoretical risks associated with live vaccines. It is not known if this is excreted in human milk; hence, caution should be used when administering vaccines to breastfeeding women. However, as an inactivated vaccine, it does not share the theoretical risks associated with live vaccines.
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