Generic Name: meningococcal conjugate vaccine (me NIN je KOK al KON je gate vax EEN)
Brand Names: Menactra, Menveo
What is Menactra?
Menactra (meningococcal conjugate vaccine) is used to prevent infection caused by meningococcal bacteria.
Menactra works by exposing you to a small dose of the bacteria or a protein from the bacteria, which causes your body to develop immunity to the disease. Meningococcal conjugate vaccine contains four of the most common types of meningococcal bacteria (serogroups A, C, W, and Y).
Meningococcal disease is a serious infection caused by a bacteria. Meningococcal bacteria can infect the spinal cord and brain, causing meningitis that can be fatal. Meningococcal disease can also lead to permanent and disabling medical problems.
Meningococcal disease can spread from one person to another through small droplets of saliva that are expelled into the air when an infected person coughs or sneezes. The bacteria can also be passed through contact with objects the infected person has touched, such as a door handle or other surface. The bacteria can also be passed through kissing, or sharing a drinking glass or eating utensil with an infected person.
Meningococcal disease is more likely to occur in babies younger than 1 year, in young people ages 16 to 23 years, in anyone with a weak immune system, and in anyone exposed to an outbreak of the disease.
Menactra is used to prevent infection caused by meningococcal bacteria. The vaccine works by exposing you to a small dose of the bacteria or a protein from the bacteria, which causes your body to develop immunity to the disease. Menactra contains four of the most common types of meningococcal bacteria (serogroups A, C, W, and Y).
Menactra will not treat an active meningococcal infection that has already developed in the body.
Menactra is for use in children and adults between the ages of 9 months and 55 years old.
Like any vaccine, Menactra may not provide protection from disease in every person.
You should not receive Menactra if you have ever had an allergic reaction to a meningococcal or diphtheria vaccine.
Before taking this medicine
You should not receive Menactra if you have ever had an allergic reaction to a meningococcal or a diphtheria vaccine.
If you have any of these other conditions, your vaccine may need to be postponed or not given at all:
pregnancy or breast-feeding;
a history of Guillain-Barré syndrome;
a history of premature birth;
a condition for which you are receiving steroids, chemotherapy, or radiation treatments; or
any condition that weakens your immune system (such as HIV, AIDS, or cancer).
You can still receive a vaccine if you have a minor cold. In the case of a more severe illness with a fever or any type of infection, wait until you get better before receiving Menactra.
It is not known whether Menactra will harm an unborn baby. However, if you are pregnant, your doctor should determine whether you need this vaccine.
If you are pregnant, your name may be listed on a pregnancy registry. This is to track the outcome of the pregnancy and to evaluate any effects of Menactra on the baby.
It is not known whether meningococcal conjugate vaccine passes into breast milk or if it could harm a nursing baby. Tell your doctor if you are breast-feeding a baby.
Menactra should not be given to anyone younger than 9 months or older than 55 years of age.
How is Menactra given?
Menactra is recommended if:
you have been exposed to an outbreak of meningococcal disease;
you are in the military;
you work in a laboratory and are exposed to meningococcal bacteria;
you live in a dormitory or other group housing;
you live in or travel to an area where meningococcal disease is common;
you have a medical problem affecting your spleen, or your spleen has been removed;
you have HIV;
you use a medicine called eculizumab (Soliris); or
you have an immune system disorder called "persistent complement component deficiency."
Menactra is given as an injection (shot) into a muscle. You will receive this injection in a doctor's office or clinic setting.
Menactra is usually given only once. Children and people who have high risks of meningococcal infection may need booster doses.
The Centers for Disease Control recommends that all teens ages 11 to 12 years be vaccinated with a single dose of Menactra. A booster dose should be given at age 16 for continued protection when teens are at highest risk of meningococcal disease.
Your booster schedule may be different from these guidelines. Follow your doctor's instructions or the schedule recommended by your local health department.
Be sure to receive all recommended doses of Menactra or you may not be fully protected against disease.
See also: Dosage Information (in more detail)
What happens if I miss a dose?
Contact your doctor if you miss a booster dose or if you get behind schedule. The next dose should be given as soon as possible. There is no need to start over.
What happens if I overdose?
An overdose of Menactra is not likely to occur.
What should I avoid before or after receiving Menactra?
Follow your doctor's instructions about any restrictions on food, beverages, or activity.
Menactra side effects
Get emergency medical help if you have signs of an allergic reaction to Menactra: hives; dizziness, weakness; fast heartbeats; difficult breathing; swelling of your face, lips, tongue, or throat.
Keep track of any and all side effects you have after receiving Menactra. When you receive a booster dose, you will need to tell the doctor if the previous shot caused any side effects.
You should not receive a booster vaccine if you had a life-threatening allergic reaction after the first shot.
Becoming infected with meningococcal disease and developing meningitis (infection of the spinal cord and lining of the brain) is much more dangerous to your health than receiving Menactra. However, like any medicine, this vaccine can cause side effects but the risk of serious side effects is extremely low.
You may feel faint after receiving Menactra. Some people have had seizure-like reactions after receiving this vaccine. Your doctor may want you to remain under observation during the first 15 minutes after the injection.
Call your doctor at once if you have:
severe weakness or unusual feeling in your arms and legs (may occur 2 to 4 weeks after you receive the vaccine);
high fever; or
Common side effects may include:
redness, pain, swelling, or a hard lump where the shot was given;
headache, drowsiness, tired feeling;
joint or muscle pain;
vomiting, loss of appetite; or
(in babies) fussiness, irritability, crying for an hour or longer.
This is not a complete list of side effects and others may occur. Call your doctor for medical advice about side effects. You may report vaccine side effects to the US Department of Health and Human Services at 1 800 822 7967.
See also: Side effects (in more detail)
What other drugs will affect Menactra?
Before receiving Menactra, tell your doctor about all other vaccines you have recently received, especially:
a diphtheria, tetanus, and pertussis vaccine (such as Daptacel); or
a pneumonia vaccine (such as Prevnar).
Also tell the doctor if you have recently received drugs or treatments that can weaken the immune system, including:
an oral, nasal, inhaled, or injectable steroid medicine;
If you are using any of these medications, you may not be able to receive the vaccine, or may need to wait until the other treatments are finished.
This list is not complete. Other drugs may interact with meningococcal conjugate vaccine, including prescription and over-the-counter medicines, vitamins, and herbal products. Not all possible interactions are listed in this medication guide.
More about Menactra (meningococcal conjugate vaccine)
- Other brands: Menveo
Related treatment guides
Where can I get more information?
- Your doctor or pharmacist can provide more information about Menactra. Additional information is available from your local health department or the Centers for Disease Control and Prevention.
- Remember, keep this and all other medicines out of the reach of children, never share your medicines with others, and use Menactra only for the indication prescribed.
- Disclaimer: Every effort has been made to ensure that the information provided by Cerner Multum, Inc. ('Multum') is accurate, up-to-date, and complete, but no guarantee is made to that effect. Drug information contained herein may be time sensitive. Multum information has been compiled for use by healthcare practitioners and consumers in the United States and therefore Multum does not warrant that uses outside of the United States are appropriate, unless specifically indicated otherwise. Multum's drug information does not endorse drugs, diagnose patients or recommend therapy. Multum's drug information is an informational resource designed to assist licensed healthcare practitioners in caring for their patients and/or to serve consumers viewing this service as a supplement to, and not a substitute for, the expertise, skill, knowledge and judgment of healthcare practitioners. The absence of a warning for a given drug or drug combination in no way should be construed to indicate that the drug or drug combination is safe, effective or appropriate for any given patient. Multum does not assume any responsibility for any aspect of healthcare administered with the aid of information Multum provides. The information contained herein is not intended to cover all possible uses, directions, precautions, warnings, drug interactions, allergic reactions, or adverse effects. If you have questions about the drugs you are taking, check with your doctor, nurse or pharmacist.
Copyright 1996-2017 Cerner Multum, Inc. Version: 7.01.
Last reviewed: May 15, 2011
Date modified: November 30, 2016