Archive for the ‘bacterial vaccines’ Category

Vivotif Berna

Vivotif Berna

Generic Name: typhoid vaccine (live), oral (TYE foid vax EEN)

What is typhoid vaccine?

Typhoid (also called “typhoid fever”) is a serious disease caused by Salmonella typhi bacteria. Typhoid can be fatal if left untreated.

Typhoid can cause high fever, muscle aches, severe headache, weakness, confusion or agitation, loss of appetite, stomach pain, diarrhea or constipation, and rose-colored spots on the skin.

Untreated typhoid infection may lead to kidney failure, or intestinal bleeding caused by perforation (forming of a hole), which can be fatal. If the infection spreads to the gallbladder, the infected person may become a chronic carrier of the bacteria that causes typhoid. A carrier may have no symptoms but is capable of spreading the infection to others.

Typhoid is spread through contact with the stool (bowel movements) of a person infected with the bacteria. This usually occurs by eating food or drinking water that has become contaminated with feces from an infected person. Once in the digestive tract, typhoid infection can spread to the blood and other parts of the body.

Typhoid fever is most common in non-industrialized parts of the world, especially Asia, Africa, and Central or South America. People who travel to those regions are at risk of coming into contact with the disease.

The typhoid vaccine is used to help prevent this disease in adults and children who are at least 6 years old. Although not part of a routine immunization schedule in the U.S., typhoid vaccine is recommended for people who travel to areas where the disease is common.

This vaccine works by exposing you to a small amount of the bacteria, which causes your body to develop immunity to the disease.

Typhoid vaccine will not treat an active infection that has already developed in the body, and will not prevent any disease caused by bacteria other than Salmonella typhi.

Like any vaccine, the typhoid vaccine may not provide protection from disease in every person.

What is the most important information I should know about typhoid vaccine?

You should not receive this vaccine if you have ever had an allergic reaction to typhoid vaccine in the past, or if you have fever with any type of infection or illness, or a weak immune system caused by disease or by using certain medicines such as chemotherapy. Typhoid vaccine should not be used in a person who is a typhoid carrier.

Before you receive this vaccine, tell the doctor if you have any illness with vomiting or diarrhea, if you are taking an antibiotic or sulfa drug (Azulfidine, Bactrim, Cotrim, Gantrisin, Septra, SMX-TMP, Sulfazine), or if you plan to start taking an anti-malaria medication within 10 days after receiving typhoid vaccine.

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, the doctor may ask you to wait until you get better before you can receive the vaccine.

The typhoid oral vaccine is given in a series of 4 capsules that are taken 1 per day on alternating days (days 1, 3, 5, and 7). On this alternating-day schedule, you will take 1 capsule every 48 hours for 7 days. You must take each capsule according to the recommended schedule for this vaccine to be effective.

You should complete all doses at least 1 week before your scheduled travel or possible exposure to typhoid.

You must keep typhoid vaccine capsules cold when not in use. Once you receive the capsules from your doctor or pharmacy, take them directly home and place them in the refrigerator. Keep each capsule in the foil blister pack in the refrigerator until you are ready to take it. Do not allow the capsules to freeze.

Like any vaccine, the typhoid vaccine may not provide protection from disease in every person.

In addition to receiving typhoid vaccine, take precautions while traveling such as avoiding raw fruits or vegetables that cannot be peeled, drinks that contain ice, flavored ices that may have been made with contaminated water, unbottled or unboiled water, or any food or beverage purchased from a street vendor.

What should I discuss with my healthcare provider before receiving typhoid vaccine?

Typhoid vaccine should not be used in a person who is a typhoid carrier. You should not receive this vaccine if you have ever had an allergic reaction to typhoid vaccine in the past, or if you have:

fever with any type of infection or illness;

a weak immune system caused by disease such as HIV/AIDS or cancer; or

a weak immune system caused by using certain medicines such as chemotherapy.

You may not be able to receive this vaccine if you have:

stomach flu or any illness with vomiting or diarrhea;

if you are taking an antibiotic, especially a sulfa drug such as sulfasalazine (Azulfidine, Sulfazine), sulfamethoxazole (Bactrim, Cotrim, Septra, SMX-TMP), or sulfisoxazole (Gantrisin); or

if you plan to start taking an anti-malaria medication within 10 days after receiving a typhoid oral vaccine.

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, the doctor may ask you to wait until you get better before you can receive the vaccine.

Vaccines may be harmful to an unborn baby and generally should not be given to a pregnant woman. However, not vaccinating the mother could be more harmful to the baby if the mother becomes infected with a disease that this vaccine could prevent. Your doctor will decide whether you should receive this vaccine, especially if you have a high risk of infection with typhoid. It is not known whether typhoid vaccine passes into breast milk, or if it could harm a nursing baby. Do not receive this vaccine without telling your doctor if you are breast-feeding a baby.

How is typhoid vaccine given?

Typhoid vaccine is recommended for adults and children in the following situations:

people who travel to countries where typhoid fever is common;

people who will have long-term exposure to food or water that may be contaminated with typhoid;

people who live with someone who is a typhoid carrier; and

laboratory workers who may come into contact with Salmonella typhi in a work setting.

The typhoid oral vaccine is given in a series of 4 capsules that are taken 1 per day on alternating days (days 1, 3, 5, and 7). On this alternating-day schedule, you will take 1 capsule every 48 hours for 7 days. You must take each capsule according to the recommended schedule for this vaccine to be effective.

You should complete all doses at least 1 week before your scheduled travel or possible exposure to typhoid.

You must keep typhoid vaccine capsules cold when not in use. Once you receive the capsules from your doctor or pharmacy, take them directly home and place them in the refrigerator. Keep each capsule in the foil blister pack in the refrigerator until you are ready to take it. Do not allow the capsules to freeze. Take the capsule on an empty stomach, at least 1 hour before a meal.

Swallow the capsule as quickly as possible after placing it in your mouth. Take with a full glass of cold or lukewarm water or other beverage. Do not use warm or hot drinks such as coffee, tea, or warm milk. The liquid you use to help swallow the typhoid vaccine capsule should not be warmer than your body temperature (98.6 degrees F).

Do not crush, chew, or break a typhoid vaccine capsule. Swallow the pill whole. The enteric-coated pill has a special coating to release the vaccine slowly into your body. Breaking the pill could damage this coating.

The complete series of 4 vaccine capsules should provide protection against typhoid for up to 5 years. Another series of 4 capsules is then recommended every 5 years during possible exposure to typhoid. Your individual booster schedule may be different from these guidelines. Follow your doctor’s instructions or the schedule recommended by the Centers for Disease Control and Prevention (CDC).

Be sure you receive all recommended doses of this vaccine. If you do not receive the full series of capsules every 5 years during continued exposure, you may not be fully protected against the disease.

Wash your hands often to help prevent typhoid when you are in an area where contamination is possible.

What happens if I miss a dose?

Contact your doctor if you forget to take a capsule on the scheduled day. You may need to start over to make sure you are fully protected against the disease.

Be sure to receive another series of 4 capsules every 5 years during continued exposure to typhoid.

What happens if I overdose?

An overdose of this vaccine is unlikely to occur when taken as directed.

What should I avoid before or after getting typhoid vaccine?

In addition to receiving typhoid vaccine, take precautions while traveling to further prevent coming into contact with bacteria that cause typhoid fever:

Avoid eating leafy vegetables such as spinach or lettuce, which are harder to wash properly.

Avoid eating raw fruits or vegetables that cannot be peeled, or that have been peeled by another person.

Avoid drinks that contain ice, or frozen treats and flavored ices that may have been made with contaminated water.

Avoid eating foods you have not cooked or prepared yourself. Use clean surfaces and utensils when preparing food.

Drink only bottled water (carbonated is best) or water that has been boiled for at least 1 minute.

Avoid any food or beverage purchased from a street vendor.

Typhoid vaccine side effects

You should not receive a booster dose if you had a life-threatening allergic reaction after taking a typhoid vaccine capsule.

Becoming infected with typhoid is much more dangerous to your health than receiving the vaccine to protect against it. Like any medicine, this vaccine can cause side effects, but the risk of serious side effects is extremely low.

Get emergency medical help if you have any of these signs of an allergic reaction: hives; difficulty breathing; swelling of your face, lips, tongue, or throat.

Less serious side effects include:

low fever;

headache;

nausea, vomiting, diarrhea, stomach pain; or

mild skin rash.

This is not a complete list of side effects and others may occur. Tell your doctor about any unusual or bothersome side effect. You may report side effects to FDA at 1-800-FDA-1088.

What other drugs will affect typhoid vaccine?

Before receiving this vaccine, tell the doctor about all other vaccines you have recently received.

You should not take an anti-malaria medication called proguanil (Malarone) for at least 10 days after you have received your last dose of typhoid vaccine. Proguanil may make typhoid vaccine less effective.

There may be other drugs that can affect this vaccine. Tell your doctor about all the prescription and over-the-counter medications you use. This includes vitamins, minerals, herbal products, and drugs prescribed by other doctors. Do not start using a new medication without telling your doctor.

Typhim Vi

Typhim Vi

Typhim Vi is used for:

Preventing typhoid fever in persons 2 years of age and older who are at increased risk because they are traveling to an area where this infection is more common, have been in contact with infected individuals, or work in an environment that increases their risk (eg, lab work).

Typhim Vi is a vaccine. It works by stimulating the immune system of the person who receives the vaccine to make their own protective antibodies against this disease.

Do NOT use Typhim Vi if:

Contact your doctor or health care provider right away if any of these apply to you.

Before using Typhim Vi :

Some medical conditions may interact with Typhim Vi . Tell your doctor or pharmacist if you have any medical conditions, especially if any of the following apply to you:

Some MEDICINES MAY INTERACT with Typhim Vi . Tell your health care provider if you are taking any other medicines, especially any of the following:

This may not be a complete list of all interactions that may occur. Ask your health care provider if Typhim Vi may interact with other medicines that you take. Check with your health care provider before you start, stop, or change the dose of any medicine.

How to use Typhim Vi :

Use Typhim Vi as directed by your doctor. Check the label on the medicine for exact dosing instructions.

Ask your health care provider any questions you may have about how to use Typhim Vi .

Important safety information:

Possible side effects of Typhim Vi :

All medicines may cause side effects, but many people have no, or minor, side effects.

Diarrhea; fever; general body discomfort; headache; muscle pain; nausea; tenderness, pain, redness, swelling, and hardening at the injection site.

Severe allergic reactions (rash; hives; itching; difficulty breathing; tightness in the chest; swelling of the mouth, face, lips, or tongue); difficulty swallowing; giant hives; hoarseness; shock.

This is not a complete list of all side effects that may occur. If you have questions about side effects, contact your health care provider. Call your doctor for medical advice about side effects. You may report side effects to FDA at 1-800-FDA-1088. You may also report side effects at

If OVERDOSE is suspected:

Contact 1-800-222-1222 (the American Association of Poison Control Centers), your local poison control center (

Typhim Vi is usually handled and stored by a health care provider. If you are using Typhim Vi at home, store Typhim Vi as directed by your pharmacist or health care provider.

General information:

This information is a summary only. It does not contain all information about Typhim Vi . If you have questions about the medicine you are taking or would like more information, check with your doctor, pharmacist, or other health care provider.

More Typhim Vi resources

Compare Typhim Vi with other medications for the treatment of:

Tice BCG Vaccine

Tice BCG Vaccine

Generic Name: BCG (bee cee jee)

What is Tice BCG Vaccine (BCG)?

BCG (Bacillus Calmette and Guérin) is made using the organisms of a bacteria.

This medication is injected directly into the bladder, where it causes inflammation and increases certain white blood cells known as natural killer cells. These killer cells act to destroy invading cells such as tumor cells in the bladder.

BCG is used to treat bladder cancer that is localized (has not spread to other parts of the body).

BCG may also be used for other purposes not listed in this medication guide.

What is the most important information I should know about Tice BCG Vaccine (BCG)?

You should not be treated with this medication if you are allergic to BCG, or if you have tuberculosis, a fever, a bladder infection, blood in your urine, or a weak immune system (caused by certain drugs or disease such as AIDS, leukemia, or lymphoma).

You should also not receive BCG if you have had a bladder biopsy, surgery, or catheter within the past 14 days.

Before you receive BCG, tell your doctor if you are allergic to latex rubber, or if you have myasthenia gravis, a pacemaker or other artificial heart device, an artificial joint or other prosthetic, or any type of infection (including HIV).

Also tell your doctor if you have ever had tuberculosis, bypass surgery, or an aneurysm (dilated blood vessel), or if you currently need to have an organ transplant (kidney, liver, heart, etc).

Your doctor may ask you to drink extra fluids for several hours after your BCG treatment to help flush out your bladder. Follow your doctor’s instructions about the type and amount of liquids you should drink.

Call your doctor right away if you have a fever after receiving BCG, especially if the fever lasts for several hours or longer. Antibiotics can make BCG less effective and should be avoided during your treatment with BCG. If you have an infection that must be treated with an antibiotic, you may need to stop receiving BCG for a short time. Follow your doctor’s instructions and be sure to tell any other doctor who treats you that you are receiving BCG.

What should I discuss with my health care provider before I receive Tice BCG Vaccine (BCG)?

You should not receive this medication if you are allergic to BCG, or if you have:

tuberculosis;

a weak immune system from diseases such as AIDS, leukemia, or lymphoma;

fever, a bladder infection, or blood in your urine;

if you are using steroids or receiving chemotherapy or radiation treatments; or

if you have had a bladder biopsy, surgery, or catheter within the past 14 days.

Before you receive BCG, tell your doctor if you are allergic to latex rubber, or if you have:

any type of bacterial, fungal, or viral infection (including HIV);

myasthenia gravis;

a pacemaker or other artificial heart device;

an artificial joint or other prosthetic;

a history of aneurysm (dilated blood vessel);

if you have ever had bypass surgery;

if you have ever had tuberculosis; or

if you need to have an organ transplant (kidney, liver, heart, etc).

If you have any of these conditions, you may need a dose adjustment or special tests to safely receive BCG.

FDA pregnancy category C. This medication may be harmful to an unborn baby. Before you receive BCG, tell your doctor if you are pregnant. Use effective birth control, and tell your doctor if you become pregnant during treatment. It is not known whether BCG passes into breast milk or if it could harm a nursing baby. Do not use this medication without telling your doctor if you are breast-feeding a baby.

How is BCG given?

BCG is a freeze-dried product that is mixed with saline and other diluents (liquids) in an amount equal to approximately 8 ounces. This liquid mixture is injected directly into the bladder using a catheter inserted into the urethra (the tube for passing urine out of your bladder). You will receive this medication in a clinic or hospital setting.

This medication is usually given once every week for 6 weeks, and then given every 3 to 6 months for up to 2 years. Follow your doctor’s instructions about your specific dosing schedule.

After BCG is placed into the bladder, you will need hold the medication in your bladder as long as possible up to 2 hours. During that time you may be encouraged to lie down or stay relaxed.

For at least 6 hours after you are treated with BCG, your urine will still contain some of the medication and the bacteria it is made from. To prevent the spread of this bacteria, use a toilet rather than a urinal, and sit on the toilet while urinating.

Before you flush the toilet, disinfect the urine with household bleach in an amount that is approximately equal to how much you have urinated. Pour the bleach into the toilet in which you urinated, let it stand for 15 minutes and then flush.

Your doctor may ask you to drink extra fluids for several hours after your BCG treatment to help flush out your bladder. Follow your doctor’s instructions about the type and amount of liquids you should drink.

Call your doctor right away if you have a fever after receiving BCG, especially if the fever lasts for several hours or longer.

Being treated with BCG can cause you to have unusual results with certain medical tests. Tell any doctor who treats you that you are using BCG.

What happens if I miss a dose?

Call your doctor for instructions if you miss an appointment for your BCG treatment.

What happens if I overdose?

Seek emergency medical attention if you think you have received too much of this medicine.

Overdose symptoms may include signs of an infection, such as fever, chills, body aches, weakness, or other flu symptoms.

What should I avoid while receiving Tice BCG Vaccine (BCG)?

Antibiotics can make BCG less effective and should be avoided during your treatment with BCG. If you have an infection that must be treated with an antibiotic, you may need to stop receiving BCG for a short time. Follow your doctor’s instructions and be sure to tell any other doctor who treats you that you are receiving BCG.

Tice BCG Vaccine (BCG) side effects

Get emergency medical help if you have any of these signs of an allergic reaction: hives; difficulty breathing; swelling of your face, lips, tongue, or throat. Report any side effects to your doctor. Some side effects may be serious, including:

fever, chills, cough, body aches, joint pain, weakness, vomiting, or other flu symptoms;

nausea, vomiting, stomach pain, jaundice (yellowing of your skin or eyes);

pain or burning when you urinate;

difficult urination;

more frequent or urgent urinating;

blood in your urine, lower back pain;

pain or swelling in your testicles;

easy bruising or bleeding;

eye pain, redness, watering, severe burning or itching; or

vision changes, increased sensitivity to light.

Less serious side effects may include:

mild nausea, stomach pain, or loss of appetite;

mild bladder or groin pain;

urine leakage or incontinence;

diarrhea, constipation;

headache;

mild skin rash;

dizziness, tired feeling; or

tissue particles in your urine (not blood).

This is not a complete list of side effects and others may occur. Tell your doctor about any unusual or bothersome side effect. You may report side effects to FDA at 1-800-FDA-1088.

What other drugs will affect Tice BCG Vaccine (BCG)?

Before you receive BCG, tell your doctor if you are taking an antibiotic, or if you are using any drugs that weaken your immune system, such as:

cancer medicine or radiation;

cyclosporine (Neoral, Sandimmune, Gengraf);

sirolimus (Rapamune), tacrolimus (Prograf);

basiliximab (Simulect), efalizumab (Raptiva), muromonab-CD3 (Orthoclone);

mycophenolate mofetil (CellCept);

azathioprine (Imuran), leflunomide (Arava), etanercept (Enbrel); or

steroids such as prednisone, fluticasone (Advair), mometasone (Asmanex, Nasonex), dexamethasone (Decadron, Hexadrol) and others.

This list is not complete and there may be other drugs that can interact with BCG. Tell your doctor about all your prescription and over-the-counter medications, vitamins, minerals, herbal products, and drugs prescribed by other doctors. Do not start a new medication without telling your doctor.

Tice BCG

Tice BCG

Tice BCG contains live bacteria. It must be prepared, handled, and disposed of as biohazard material. Serious infections have been reported by health care providers after accidental needle sticks during preparation and handling of Tice BCG . Patients with weakened immune systems have become infected when their injection medicines are prepared in the same area as Tice BCG . Serious, sometimes fatal, infections have also occurred in patients receiving Tice BCG through a catheter.

Tice BCG is used for:

Treating cancer of the bladder.

Tice BCG is a strain of bacteria. How it works is not fully known. It is thought to stimulate the immune system.

Do NOT use Tice BCG if:

Contact your doctor or health care provider right away if any of these apply to you.

Before using Tice BCG :

Some medical conditions may interact with Tice BCG . Tell your doctor or pharmacist if you have any medical conditions, especially if any of the following apply to you:

Some MEDICINES MAY INTERACT with Tice BCG . Tell your health care provider if you are taking any other medicines, especially any of the following:

This may not be a complete list of all interactions that may occur. Ask your health care provider if Tice BCG may interact with other medicines that you take. Check with your health care provider before you start, stop, or change the dose of any medicine.

How to use Tice BCG :

Use Tice BCG as directed by your doctor. Check the label on the medicine for exact dosing instructions.

Ask your health care provider any questions you may have about how to use Tice BCG .

Important safety information:

Possible side effects of Tice BCG :

All medicines may cause side effects, but many people have no, or minor, side effects.

Diarrhea; increased pain or frequency of urination; loss of appetite; nausea; stomach pain.

Severe allergic reactions (rash; hives; itching; difficulty breathing; tightness in the chest; swelling of the mouth, face, lips, or tongue); blood in urine; burning or pain when urinating; chills; cough; fever; flu-like symptoms; frequent or urgent urination; general feeling of discomfort; joint pain; tiredness; vomiting.

This is not a complete list of all side effects that may occur. If you have questions about side effects, contact your health care provider. Call your doctor for medical advice about side effects. You may report side effects to FDA at 1-800-FDA-1088. You may also report side effects at

If OVERDOSE is suspected:

Contact 1-800-222-1222 (the American Association of Poison Control Centers), your local poison control center (

Tice BCG is usually handled and stored by a health care provider. If you are using Tice BCG at home, store Tice BCG as directed by your pharmacist or health care provider. Keep Tice BCG out of the reach of children and away from pets.

General information:

This information is a summary only. It does not contain all information about Tice BCG . If you have questions about the medicine you are taking or would like more information, check with your doctor, pharmacist, or other health care provider.

More Tice BCG resources

TheraCys

TheraCys

TheraCys contains live bacteria. It must be prepared, handled, and disposed of as biohazard material. Serious infections have been reported by health care providers after accidental needle sticks during preparation and handling of TheraCys . Patients with weakened immune systems have become infected when their injection medicines are prepared in the same area as TheraCys . Serious, sometimes fatal, infections have also occurred in patients receiving TheraCys through a catheter.

TheraCys is used for:

Treating cancer of the bladder.

TheraCys is a strain of bacteria. How it works is not fully known. It is thought to stimulate the immune system.

Do NOT use TheraCys if:

Contact your doctor or health care provider right away if any of these apply to you.

Before using TheraCys :

Some medical conditions may interact with TheraCys . Tell your doctor or pharmacist if you have any medical conditions, especially if any of the following apply to you:

Some MEDICINES MAY INTERACT with TheraCys . Tell your health care provider if you are taking any other medicines, especially any of the following:

This may not be a complete list of all interactions that may occur. Ask your health care provider if TheraCys may interact with other medicines that you take. Check with your health care provider before you start, stop, or change the dose of any medicine.

How to use TheraCys :

Use TheraCys as directed by your doctor. Check the label on the medicine for exact dosing instructions.

Ask your health care provider any questions you may have about how to use TheraCys .

Important safety information:

Possible side effects of TheraCys :

All medicines may cause side effects, but many people have no, or minor, side effects.

Diarrhea; increased pain or frequency of urination; loss of appetite; nausea; stomach pain.

Severe allergic reactions (rash; hives; itching; difficulty breathing; tightness in the chest; swelling of the mouth, face, lips, or tongue); blood in urine; burning or pain when urinating; chills; cough; fever; flu-like symptoms; frequent or urgent urination; general feeling of discomfort; joint pain; tiredness; vomiting.

This is not a complete list of all side effects that may occur. If you have questions about side effects, contact your health care provider. Call your doctor for medical advice about side effects. You may report side effects to FDA at 1-800-FDA-1088. You may also report side effects at

If OVERDOSE is suspected:

Contact 1-800-222-1222 (the American Association of Poison Control Centers), your local poison control center (

TheraCys is usually handled and stored by a health care provider. If you are using TheraCys at home, store TheraCys as directed by your pharmacist or health care provider. Keep TheraCys out of the reach of children and away from pets.

General information:

This information is a summary only. It does not contain all information about TheraCys . If you have questions about the medicine you are taking or would like more information, check with your doctor, pharmacist, or other health care provider.

More TheraCys resources

Compare TheraCys with other medications for the treatment of:

Prevnar

Prevnar

Generic Name: pneumococcal conjugate vaccine (PCV-pediatric only), 7-valent (NOO moe KOK al KON joo gate)

What is Prevnar?

Prevnar containea pneumococcal conjugate vaccine (PCV) and is used to prevent infection caused by pneumococcal bacteria. PCV contains 7 different types of pneumococcal bacteria.

Prevnar works by exposing your child to a small dose of the bacteria or a protein from the bacteria, which causes the body to develop immunity to the disease. Prevnar will not treat an active infection that has already developed in the body.

Prevnar is for use only in children between the ages of 6 weeks and 10 years. For adults and children who are 2 years of age and older, another vaccine called Pneumovax (pneumococcal polysaccharides vaccine [PPV] 23-valent) is used.

Becoming infected with pneumococcal disease (such as pneumonia or meningitis) is much more dangerous to your child’s health than receiving the vaccine to protect against it. Like any medicine, Prevnar can cause side effects, but the risk of serious side effects is extremely low.

Like any vaccine, Prevnar may not provide protection from disease in every person.

Important information about Prevnar

Prevnar is given in a series of shots. The first shot is usually given when the child is 2 months old. The booster shots are then given at 4 months, 6 months, and 12 to 15 months of age.

In a child older than 6 months who has not yet received a Prevnar, the first dose can be given any time from the age of 7 months through 9 years.

If the child is less than 1 year old at the time of the first shot, he or she will need 2 booster doses. If the child is 12 to 23 months old at the time of the first shot, he or she will need 1 booster dose. A child who is 2 years or older at the time of the first shot may need only the one shot and no booster doses.

The timing of this vaccination is very important for it to be effective. Your child’s individual booster schedule may be different from these guidelines. Follow your doctor’s instructions or the schedule recommended by the health department of the state you live in. Keep track of any and all side effects your child has after receiving Prevnar. If the child ever has to receive another PCV in the future, you will need to tell the doctor if the first shot caused any side effects.

Your child can still receive a vaccine if he or she has a cold or fever. In the case of a more severe illness with a fever or any type of infection, wait until the child gets better before receiving Prevnar.

Becoming infected with pneumococcal disease (such as pneumonia or meningitis) is much more dangerous to your child’s health than receiving the vaccine to protect against it. Like any medicine, Prevnar can cause side effects, but the risk of serious side effects is extremely low.

Be sure to keep your child on a regular schedule for other immunizations against diseases such as diphtheria, tetanus, pertussis (whooping cough), measles, mumps, hepatitis, or varicella (chicken pox). Your doctor or state health department can provide you with a recommended immunization schedule.

Before receiving Prevnar

Keep track of any and all side effects your child has after receiving Prevnar. If the child ever has to receive another pneumococcal vaccine in the future, you will need to tell the doctor if the first shot caused any side effects. Your child should not receive Prevnar if he or she has ever had an allergic reaction to a pneumococcal vaccine, or if the child has received cancer chemotherapy or radiation treatment in the past 3 months.

Before receiving Prevnar, tell your doctor if your child is allergic to any drugs, or if the child has:

a bleeding or blood clotting disorder such as hemophilia or easy bruising;

a history of seizures;

an allergy to latex rubber;

a weak immune system caused by disease, bone marrow transplant, or by using certain medicines or receiving cancer treatments; or

if the child is taking a blood thinner such as warfarin (Coumadin).

Your child can still receive a vaccine if he or she has a cold or fever. In the case of a more severe illness with a fever or any type of infection, wait until the child gets better before receiving Prevnar.

How is Prevnar given?

Prevnar is given as an injection (shot) into a muscle. Your child will receive this injection in a doctor’s office or other clinic setting.

Prevnar is given in a series of shots. The first shot is usually given when the child is 2 months old. The booster shots are then given at 4 months, 6 months, and 12 to 15 months of age.

The first Prevnar injection should be given no earlier than 6 weeks of age. Allow at least 2 months to pass between injections.

If your child is already 6 months or older, he or she can still receive Prevnar on the following schedule:

Age 7-11 months: two injections at least 4 weeks apart, followed by a third injection after the child turns 1 year (at least 2 months after the second injection);

Age 12-23 months: two injections at least 2 months apart;

Age 2-9 years: one injection.

A child who is 24 to 59 months old may need 1 or 2 additional doses of Prevnar if the child did not receive all recommended doses on a prior schedule, or if the child has a certain medical condition or weakened immune system.

Your doctor may recommend treating fever and pain with an aspirin-free pain reliever such as acetaminophen (Tylenol) or ibuprofen (Motrin, Advil, and others) when the shot is given and for the next 24 hours. Follow the label directions or your doctor’s instructions about how much of this medicine to give your child.

It is especially important to prevent fever from occurring in a child who has a seizure disorder such as epilepsy.

Be sure to keep your child on a regular schedule for other immunizations such as diphtheria, tetanus, pertussis (whooping cough), hepatitis, and varicella (chicken pox). Your doctor or state health department can provide you with a recommended immunization schedule.

What happens if I miss a dose?

Contact your doctor if your child will miss a booster dose or gets behind schedule. The next dose should be given as soon as possible. There is no need to start over.

Be sure your child receives all recommended doses of Prevnar. If your child does not receive the full series of vaccines, he or she may not be fully protected against the disease.

What happens if I overdose?

An overdose of Prevnar is unlikely to occur.

What should I avoid before or after receiving Prevnar?

Avoid Prevnar while your child is undergoing chemotherapy or radiation treatments. You may need to wait until it has been several months after your child has completed his or her treatments. Follow your doctor’s instructions.

Prevnar side effects

Your child should not receive a booster vaccine if he or she had a life-threatening allergic reaction after the first shot. Keep track of any and all side effects your child has after receiving Prevnar. When the child receives a booster dose, you will need to tell the doctor if the previous shots caused any side effects.

Becoming infected with pneumococcal disease (such as pneumonia or meningitis) is much more dangerous to your child’s health than receiving the vaccine to protect against it. Like any medicine, Prevnar can cause side effects, but the risk of serious side effects is extremely low.

Get emergency medical help if your child has any of these signs of an allergic reaction: hives; difficulty breathing; swelling of the face, lips, tongue, or throat. Call your doctor at once if your child has any of these serious side effects:

high fever (103 degrees or higher);

seizure (convulsions);

easy bruising or bleeding; or

severe pain, itching, irritation, or skin changes where the shot was given.

Less serious side effects include

mild soreness, redness, swelling, or a hard lump where the shot was given;

weakness, tired feeling;

crying, fussiness;

drowsiness, restless sleep;

low fever (102 degrees or less);

vomiting, diarrhea, loss of appetite; or

mild skin rash.

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 side effects to FDA at 1-800-FDA-1088.

What other drugs will affect Prevnar?

Before receiving Prevnar, tell the doctor about all other vaccines your child has recently received.

Also tell the doctor if your child has recently received drugs or treatments that can weaken the immune system, including:

an oral, nasal, inhaled, or injectable steroid medicine;

medications to treat psoriasis, rheumatoid arthritis, or other autoimmune disorders, such as azathioprine (Imuran), efalizumab (Raptiva), etanercept (Enbrel), leflunomide (Arava), and others; or

medicines to treat or prevent organ transplant rejection, such as basiliximab (Simulect), cyclosporine (Sandimmune, Neoral, Gengraf), muromonab-CD3 (Orthoclone), mycophenolate mofetil (CellCept), sirolimus (Rapamune), or tacrolimus (Prograf).

If your child is using any of these medications, he or she may not be able to receive the vaccine, or may need to wait until the other treatments are finished.

There may be other drugs that can affect Prevnar. Tell your doctor about all the prescription and over-the-counter medications your child has received. This includes vitamins, minerals, herbal products, and drugs prescribed by other doctors. Do not start using a new medication without telling your child’s doctor.

Pneumovax 23

Pneumovax 23

Pneumovax 23 is used for:

Preventing certain infections.

Pneumovax 23 is a vaccine. It works by stimulating the body to make antibodies to Streptococcus pneumoniae bacteria.

Do NOT use Pneumovax 23 if:

Contact your doctor or health care provider right away if any of these apply to you.

Before using Pneumovax 23 :

Some medical conditions may interact with Pneumovax 23 . Tell your doctor or pharmacist if you have any medical conditions, especially if any of the following apply to you:

Some MEDICINES MAY INTERACT with Pneumovax 23 . Tell your health care provider if you are taking any other medicines, especially any of the following:

This may not be a complete list of all interactions that may occur. Ask your health care provider if Pneumovax 23 may interact with other medicines that you take. Check with your health care provider before you start, stop, or change the dose of any medicine.

How to use Pneumovax 23 :

Use Pneumovax 23 as directed by your doctor. Check the label on the medicine for exact dosing instructions.

Ask your health care provider any questions you may have about how to use Pneumovax 23 .

Important safety information:

Possible side effects of Pneumovax 23 :

All medicines may cause side effects, but many people have no, or minor, side effects.

Fever; redness, soreness, swelling, or a lump at the injection site.

Severe allergic reactions (rash; hives; itching; difficulty breathing; tightness in the chest; swelling of the mouth, face, lips, or tongue); weakness.

This is not a complete list of all side effects that may occur. If you have questions about side effects, contact your health care provider. Call your doctor for medical advice about side effects. You may report side effects to FDA at 1-800-FDA-1088. You may also report side effects at

If OVERDOSE is suspected:

Contact 1-800-222-1222 (the American Association of Poison Control Centers), your local poison control center (

Store in the refrigerator, between 36 and 46 degrees F (2 and 8 degrees C). Do not use past the expiration date. Keep Pneumovax 23 out of the reach of children and away from pets.

General information:

This information is a summary only. It does not contain all information about Pneumovax 23 . If you have questions about the medicine you are taking or would like more information, check with your doctor, pharmacist, or other health care provider.

More Pneumovax 23 resources

Compare Pneumovax 23 with other medications for the treatment of:

PedvaxHIB

PedvaxHIB

PedvaxHIB is used for:

Preventing infection caused by Haemophilus influenza type b bacteria and/or diphtheria, tetanus, and pertussis.

PedvaxHIB is a vaccine. It works by stimulating the body to produce antibodies against the organism that causes H. influenza infection.

Do NOT use PedvaxHIB if:

Contact your doctor or health care provider right away if any of these apply to you.

Before using PedvaxHIB :

Some medical conditions may interact with PedvaxHIB . Tell your doctor or pharmacist if you have any medical conditions, especially if any of the following apply to you:

Some MEDICINES MAY INTERACT with PedvaxHIB . However, no specific interactions with PedvaxHIB are known at this time.

This may not be a complete list of all interactions that may occur. Ask your health care provider if PedvaxHIB may interact with other medicines that you take. Check with your health care provider before you start, stop, or change the dose of any medicine.

How to use PedvaxHIB :

Use PedvaxHIB as directed by your doctor. Check the label on the medicine for exact dosing instructions.

Ask your health care provider any questions you may have about how to use PedvaxHIB .

Important safety information:

Possible side effects of PedvaxHIB :

All medicines may cause side effects, but many people have no, or minor, side effects.

Fever; irritability; redness, tenderness, pain, swelling, or a lump at the injection site; sleepiness.

Severe allergic reactions (rash; hives; difficulty breathing; tightness in the chest; swelling of the mouth, face, lips, or tongue); seizures.

This is not a complete list of all side effects that may occur. If you have questions about side effects, contact your health care provider. Call your doctor for medical advice about side effects. You may report side effects to FDA at 1-800-FDA-1088. You may also report side effects at

If OVERDOSE is suspected:

Contact 1-800-222-1222 (the American Association of Poison Control Centers), your local poison control center (

PedvaxHIB is usually handled and stored by a health care provider. If you are using PedvaxHIB at home, store PedvaxHIB as directed by your pharmacist or health care provider. Keep PedvaxHIB out of the reach of children and away from pets.

General information:

This information is a summary only. It does not contain all information about PedvaxHIB . If you have questions about the medicine you are taking or would like more information, check with your doctor, pharmacist, or other health care provider.

More PedvaxHIB resources

MRV

MRV

Generic Name: mixed respiratory vaccine (MIXED RESP i ra tor ee VAK een)

What is MRV (mixed respiratory vaccine)?

Mixed respiratory vaccine is a mixture of killed bacteria. It is used to strengthen the immune system to help your body fight chronic infections.

Mixed respiratory vaccine is used in people with chronic infections such as infectious asthma, chronic sinusitis (inflamation of the sinuses), nasal polyps, ear infections, and other upper respiratory tract infections.

The vaccine works by exposing you to a small dose of the bacteria mixture, which causes the body to develop immunity to certain diseases. This vaccine will not treat an active infection that has already developed in the body.

Like any vaccine, the mixed respiratory vaccine may not provide protection from disease in every person.

What is the most important information I should know about MRV (mixed respiratory vaccine)?

You should not receive this vaccine if have rheumatoid arthritis, systemic lupus erythematosus (SLE), or any other connective tissue disorders such as Marfan syndrome, Ehlers-Danlos syndrome, osteogenesis imperfecta, or scleroderma.

Before receiving mixed respiratory vaccine, tell your doctor if you have diabetes or eczema.

The mixed respiratory vaccine is usually given every several days. The first shot is usually given at a larger dose. The booster shots are then given at gradually smaller doses as your body begins to respond to the vaccine. After several months, your shots may be spaced farther apart, or you may need them only every other week.

The vaccine works by exposing you to a small dose of a bacteria mixture, which causes the body to develop immunity to certain diseases. This vaccine will not treat an active infection that has already developed in the body.

What should I discuss with my healthcare provider before receiving this vaccine?

You should not receive this vaccine if have:

rheumatoid arthritis;

lupus erythematosus (SLE); or

other connective tissue disorders such as Marfan syndrome, Ehlers-Danlos syndrome, osteogenesis imperfecta, or scleroderma.

Before receiving this vaccine, tell your doctor if you have:

diabetes; or

eczema.

You can still receive a vaccine if you have a cold or fever. In the case of a more severe illness with a fever or any type of infection, wait until you get better before receiving this vaccine.

FDA pregnancy category C. This medication may be harmful to an unborn baby. Tell your doctor if you are pregnant or plan to become pregnant during treatment. It is not known whether mixed respiratory vaccine passes into breast milk. Do not receive this vaccine without telling your doctor if you are breast-feeding a baby.

How should I use MRV (mixed respiratory vaccine)?

This vaccine is given as an injection (shot) under the skin. You will receive this injection in a doctor’s office or other clinic setting.

The mixed respiratory vaccine is usually given every several days. The first shot is usually given at a larger dose. The booster shots are then given at gradually smaller doses as your body begins to respond to the vaccine. After several months, your shots may be spaced farther apart, or you may need them only every other week.

Your individual vaccination schedule may be different from these guidelines. Follow your doctor’s instructions.

Your doctor may recommend treating fever and pain with an aspirin-free pain reliever such as acetaminophen (Tylenol) or ibuprofen (Motrin, Advil, and others) when the shot is given and for the next 24 hours. Follow the label directions or your doctor’s instructions about how much of this medicine to take.

It is especially important to prevent fever from occurring if you have a seizure disorder such as epilepsy.

What happens if I miss a dose?

Contact your doctor if you will 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.

Be sure you receive all recommended doses of this vaccine. If you do not receive the full series of vaccines, you may not be fully protected against the disease.

What happens if I overdose?

An overdose of this vaccine is unlikely to occur.

What should I avoid while using MRV (mixed respiratory vaccine)?

Do not receive a “live” vaccine such as measles, mumps, rubella (MMR), oral polio, yellow fever, or varicella (chickenpox) for at least 4 weeks after you have received the mixed respiratory vaccine. The other live vaccine may not work as well during this time, and may not fully protect you from disease.

MRV (mixed respiratory vaccine) side effects

You should not receive a booster vaccine if you had a life-threatening allergic reaction after the first shot. Keep track of any and all side effects you have after receiving this vaccine. When you receive a booster dose, you will need to tell the doctor if the previous shots caused any side effects. Get emergency medical help if you have any of these signs of an allergic reaction: hives; difficulty breathing; swelling of your face, lips, tongue, or throat.

Call your doctor at once if you have any of these serious side effects:

severe skin rash, itching, or swelling;

a feeling of extreme discomfort or uneasiness;

severe muscle pain; or

high fever (within a few hours or a few days after the vaccine).

Less serious side effects include:

redness, pain, swelling, or a lump where the shot was given;

minor aches and pains;

drowsiness; or

mild skin rash.

Side effects other than those listed here may also occur. Talk to your doctor about any side effect that seems unusual or that is especially bothersome.

What other drugs will affect MRV (mixed respiratory vaccine)?

Before receiving this vaccine, tell the doctor about all other vaccines you have recently received.

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;

medications to treat psoriasis, rheumatoid arthritis, or other autoimmune disorders, such as azathioprine (Imuran), efalizumab (Raptiva), etanercept (Enbrel), leflunomide (Arava), and others; or

medicines to treat or prevent organ transplant rejection, such as basiliximab (Simulect), cyclosporine (Sandimmune, Neoral, Gengraf), muromonab-CD3 (Orthoclone), mycophenolate mofetil (CellCept), sirolimus (Rapamune), or tacrolimus (Prograf).

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.

There may be other drugs that can affect this vaccine. Tell your doctor about all the prescription and over-the-counter medications you have received. This includes vitamins, minerals, herbal products, and drugs prescribed by other doctors. Do not start using a new medication without telling your doctor.

Menomune A/ C/ Y/ W-135

Menomune A/C/Y/W-135

Generic Name: meningococcal polysaccharide vaccine (me NIN je KOK al POL ee SAK a ride vax EEN)

What is Menomune A/C/Y/W-135 (meningococcal polysaccharide vaccine)?

Meningococcal disease is a serious infection caused by a bacteria. Meningococcal bacteria can infect the blood, spinal cord, and brain. These conditions can be fatal.

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 polysaccharide vaccine is used to prevent infection caused by meningococcal bacteria. The vaccine contains four of the most common types of meningococcal bacteria.

Meningococcal polysaccharide 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. This vaccine will not treat an active infection that has already developed in the body.

Meningococcal polysaccharide vaccine is for use in adults and children who are at least 3 months of age.

Like any vaccine, meningococcal polysaccharide vaccine may not provide protection from disease in every person.

Developing meningitis (infection of the spinal cord and lining of the brain) is much more dangerous to your health than receiving this vaccine. However, like any medicine, this vaccine can cause side effects but the risk of serious side effects is extremely low.

What is the most important information I should know about Menomune A/C/Y/W-135 (meningococcal polysaccharide vaccine)?

Developing meningitis (infection of the spinal cord and lining of the brain) is much more dangerous to your health than receiving this vaccine. However, like any medicine, this vaccine can cause side effects but the risk of serious side effects is extremely low.

Keep track of any and all side effects you have after receiving this vaccine. If you ever need to receive another meningococcal vaccine in the future, you will need to tell the doctor if the first shot caused any side effects. Do not receive this vaccine if you have ever had an allergic reaction to a meningococcal vaccine, or if you are allergic to a preservative called thimerosol.

Before receiving meningococcal polysaccharide vaccine, tell your doctor if you have a weak immune system, if you are allergic to latex rubber, or if you are receiving steroids, chemotherapy, or radiation treatment. If you have any of these conditions, your vaccine may need to be postponed or not given at all.

You can still receive meningococcal polysaccharide vaccine if you have a minor cold. However, if you are moderately or severely ill with a fever or any type of infection, wait until you recover before receiving this vaccine.

Like any vaccine, meningococcal polysaccharide vaccine may not provide protection from disease in every person.

What should I discuss with my healthcare provider before receiving Menomune A/C/Y/W-135 (meningococcal polysaccharide vaccine)?

Do not receive this vaccine if you have ever had an allergic reaction to a meningococcal vaccine, or if you are allergic to a preservative called thimerosol.

Before receiving meningococcal polysaccharide vaccine, tell your doctor if you are allergic to any drugs, or if you have:

any condition that weakens the immune system (such as HIV, AIDS, or cancer);

if you are receiving steroids, chemotherapy, or radiation treatments; or

if you are allergic to latex rubber.

If you have any of these conditions, you may not be able to receive meningococcal polysaccharide vaccine, or you may need to wait until your condition changes or you have completed your treatments.

FDA pregnancy category C. It is not known whether this vaccine may be harmful to an unborn baby. Before you receive the vaccine, tell your doctor if you are pregnant or plan to become pregnant soon after receiving the vaccine.

Your name may need to be listed on a registry of women who receive a meningococcal vaccine during pregnancy if you receive this vaccine while you are pregnant. The purpose of this registry is to track the outcome of your pregnancy and the birth of your child so that health department authorities are notified of any unwanted effects on the baby.

It is not known whether meningococcal polysaccharide vaccine passes into breast milk or if it could harm a nursing baby. Do not use this medication without telling your doctor if you are breast-feeding a baby. This vaccine should not be given to anyone younger than 3 months old.

How is meningococcal polysaccharide vaccine given?

This vaccine is given as a shot under the skin. Your doctor, nurse, or other healthcare provider will give you this injection.

Meningococcal polysaccharide vaccine is usually given only once. Chldren and people who have higher risks of meningococcal infection may need a repeat dose of this vaccine 2 or 3 years after receiving the first shot.

Meningococcal polysaccharide vaccine is recommended in the following situations:

for people who do not have a spleen;

for laboratory workers who are routinely exposed to meningococcal bacteria;

for people who live in dormitories or other group housing; and

for people who travel or live among certain populations where meningococcal outbreak is common.

You can still receive a meningococcal polysaccharide vaccine if you have a minor cold. However, if you are moderately or severely ill with a fever or any type of infection, wait until you recover before receiving this vaccine.

Your doctor may recommend using a non aspirin pain reliever to prevent pain or fever that can occur with this vaccination. Over-the-counter pain relievers include acetaminophen (Tylenol, Tempra, Panadol, and others) or ibuprofen (Motrin Childrens, Advil Childrens, and others). Use this medication when the shot is given and for the next 24 hours, unless your doctor tells you otherwise. Use only the dose your doctor recommends.

What happens if I miss a dose?

Since meningococcal polysaccharide vaccine is usually given as a single injection, you may not be on a booster schedule.

If your child misses a booster dose of this vaccine, call your doctor for instructions.

What happens if I overdose?

An overdose of meningococcal polysaccharide vaccine is not likely to occur.

What should I avoid before or after getting Menomune A/C/Y/W-135 (meningococcal polysaccharide vaccine)?

There are usually no restrictions on food, beverages, or activity before or after receiving meningococcal polysaccharide vaccine.

Menomune A/C/Y/W-135 (meningococcal polysaccharide vaccine) side effects

Keep track of any and all side effects you have after receiving this vaccine. If you ever need to receive another meningococcal vaccine in the future, you will need to tell the doctor if the first shot caused any side effects. Get emergency medical help if you have any of these signs of an allergic reaction: hives; difficulty breathing; swelling of your face, lips, tongue, or throat. Call your doctor at once if you have any of these serious side effects:

severe weakness or unusual feeling in your arms and legs (may occur 2 to 4 weeks after you receive the vaccine);

high fever; or

unusual bleeding.

Less serious side effects may be more likely to occur, such as:

low fever, chills;

redness, pain, swelling, or a lump where the vaccine was injected;

headache;

tired feeling;

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 side effects to FDA at 1-800-FDA-1088.

What other drugs will affect Menomune A/C/Y/W-135 (meningococcal polysaccharide vaccine)?

Before receiving this vaccine, tell your doctor if you are using a blood thinner (warfarin, Coumadin).

Meningococcal polysaccharide vaccine can be given at the same time as most other vaccinations, but should not be given together with a pertussis (whooping cough) or typhoid vaccine.

Talk to your doctor before receiving meningococcal vaccine if you are using any of the following medications that may affect the immune system:

azathioprine (Imuran);

basiliximab (Simulect);

cyclosporine (Sandimmune, Neoral, Gengraf);

etanercept (Enbrel);

leflunomide (Arava);

muromonab-CD3 (Orthoclone);

mycophenolate mofetil (CellCept);

sirolimus (Rapamune);

tacrolimus (Prograf);

chemotherapy or radiation treatment for cancer;

a steroid medicine such as betamethasone (Celestone), cortisone (Cortone), dexamethasone (Decadron, Dexone), hydrocortisone (Cortef, Hydrocortone), methylprednisolone (Medrol), prednisolone (Prelone, Pediapred), prednisone (Orasone, Deltasone), triamcinolone (Aristocort), and others; or

an inhaled or nasal steroid such as beclomethasone (Qvar, Beclovent, Beconase, Vanceril, Vancenase), budesonide (Pulmicort, Rhinocort), flunisolide (Aerobid, Nasalide, Nasarel), fluticasone (Flovent, Flonase), mometasone (Nasonex), or triamcinolone (Azmacort, Nasacort).

If you are using any of these drugs, you may not be able to receive meningococcal polysaccharide vaccine, or you may need dosage adjustments or special tests during treatment.

There may be other drugs not listed that can affect meningococcal polysaccharide vaccine. Tell your doctor about all the prescription and over-the-counter medications you use. This includes vitamins, minerals, herbal products, and drugs prescribed by other doctors. Do not start using a new medication without telling your doctor.

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