"The European Medicines Agency's Committee for Medicinal Products for Human Use (CHMP) has recommended 150 mg lamivudine/300 mg raltegravir (Dutrebis, Merck Sharp & Dohme Limited) for the treatment of HIV 1 infection in adults, adolesce"...
Read this Medication Guide before you start taking KALETRA and each time you get a refill. There may be new information. This information does not take the place of talking with your doctor about your medical condition or treatment. You and your doctor should talk about your treatment with KALETRA before you start taking it and at regular check-ups. You should stay under your doctor's care when taking KALETRA.
What is the most important information I should know about KALETRA?
KALETRA may cause serious side effects, including:
- Interactions with other medicines. It is important to know the medicines that should not be taken with KALETRA. For more information, see “Who should not take KALETRA?”
- Changes in your heart rhythm and the electrical
activity of your heart. These changes may be seen on an EKG
(electrocardiogram) and can lead to serious heart problems. Your risk for these
problems may be higher if you:
- already have a history of abnormal heart rhythm or other types of heart disease.
- take other medicines that can affect your heart rhythm while you take KALETRA.
Tell your doctor right away if you have any of these symptoms while taking KALETRA:
See “What are the possible side effects of KALETRA?” for more information about serious side effects.
What is KALETRA?
KALETRA is a prescription HIV-1 medicine that is used with other HIV medicines to treat HIV1 (Human Immunodeficiency Virus) infection in adults and children 14 days of age and older. HIV is the virus that causes AIDS (Acquired Immune Deficiency Syndrome). KALETRA is a type of HIV medicine called a protease inhibitor. KALETRA contains two medicines: lopinavir and ritonavir.
When used with other HIV medicines, KALETRA may help to reduce the amount of HIV in your blood (called “viral load”). KALETRA may also help to increase the number of white blood cells called CD4 (T) cell which help fight off other infections. Reducing the amount of HIV and increasing the CD4 (T) cell count may improve your immune system. This may reduce your risk of death or infections that can happen when your immune system is weak (opportunistic infections).
It is not known if KALETRA is safe and effective in children under 14 days old.
KALETRA does not cure HIV infection or AIDS. People taking KALETRA may develop infections or other conditions associated with HIV infection, including opportunistic infections (for example, pneumonia and herpes virus infections).
Avoid doing things that can spread HIV-1 infection to others:
- Do not share needles or other injection equipment.
- Do not share personal items that can have blood or body fluids on them, like toothbrushes and razor blades.
- Do not have any kind of sex without protection. Always practice safe sex by using a latex or polyurethane condom to lower the chance of sexual contact with semen, vaginal secretions, or blood.
Ask your doctor if you have any questions on how to prevent passing HIV to other people.
Who should not take KALETRA?
Do not take KALETRA if you take any of the following medicines:
- alfuzosin (Uroxatral®)
- cisapride (Propulsid®, Quicksolv®)
- ergot containing medicines including
- lovastatin (Advicor®, Altoprev®, Mevacor®)
- midazolam oral syrup
- pimozide (Orap®)
- rifampin (Rifadin®, Rifamate®, Rifater®, Rimactane®)
- sildenafil (Revatio®), when used for the treatment of pulmonary arterial hypertension
- simvastatin (Zocor®, Vytorin®, Simcor®)
- St. John's Wort (Hypericum perforatum)
- triazolam (Halcion®)
Serious problems can happen if you or your child take any of the medicines listed above with KALETRA.
- Do not take KALETRA if you are allergic to lopinavir, ritonavir or any of the ingredients in KALETRA. See the end of this Medication Guide for a complete list of ingredients in KALETRA.
What should I tell my doctor before taking KALETRA?
KALETRA may not be right for you. Tell your doctor about all your medical conditions, including if you:
- have any heart problems, including if you have a condition called Congenital Long QT Syndrome.
- have or had pancreas problems.
- have liver problems, including Hepatitis B or Hepatitis C.
- have diabetes.
- have hemophilia. People who take KALETRA may have increased bleeding.
- have low potassium in your blood.
- are pregnant or plan to become pregnant. It is not known
if KALETRA will harm your unborn baby.
Pregnancy Registry. There is a pregnancy registry for women who take antiretroviral medicines during pregnancy. The purpose of the pregnancy registry is to collect information about the health of you and your baby. Talk to your doctor about how you can take part in this registry.
- Do not breastfeed. We do not know if KALETRA can be passed to the baby through your breast milk and whether it could harm your baby. Also, mothers with HIV-1 should not breastfeed because HIV-1 can be passed to the baby in the breast milk.
Tell your doctor about all the medicines you take, including prescription and non-prescription medicines, vitamins, and herbal supplements. Many medicines interact with KALETRA. Do not start taking a new medicine without telling your doctor or pharmacist. Your doctor can tell you if it is safe to take KALETRA with other medicines. Your doctor may need to change the dose of other medicines while you take KALETRA.
Especially tell your doctor if you take:
- medicine to treat HIV
- estrogen-based contraceptives (birth control pills and patches ). KALETRA may reduce the effectiveness of estrogen-based contraceptives. During treatment with KALETRA, you should use a different type or an extra form of birth control. Talk to your doctor about what types of birth control you can use to prevent pregnancy while taking KALETRA.
- medicines to prevent organ transplant rejection
- medicines to treat cancer
- amiodarone (Cordarone®, Pacerone®)
- atorvastatin (Lipitor®)
- atovaquone (Marlarone®, Mepron®)
- avanafil (Stendra®), sildenafil (Viagra®), tadalafil (Cialis®), or vardenafil (Levitra®) for the treatment of erectile dysfunction (ED). If you get dizzy or faint (low blood pressure), have vision changes or have an erection that last longer than 4 hours, call your doctor or get medical help right away
- bepridil (Bepadin®, Vascor®)
- boceprevir (Victrelis®)
- bosentan (Tracleer®)
- budesonide (Rhinocort®, Symbicort®, Pulmicort®, Entocort EC®)
- bupropion (Aplenzin®, Forfivo XL®, Wellbutrin®, Zyban®)
- carbamazepine (Carbatrol®, Epitol®, Equetro®, Tegretol®)
- clarithromycin (Biaxin®, Prevpac®)
- colchicine (Colcrys®)
- dexamethasone (Maxidex®, Ozurdex®)
- fentanyl (Abstral®, Actiq®, Duragesic®, Fentora®, Lazanda®, Onsolis®, Subsys®)
- fluticasone (Cutivate®, Flonase®, Flovent®, Flovent Diskus®, Flovent HFA®, Veramyst®)
- itraconazole (Onmel®, Sporanox®)
- ketoconazole (Extina®, Ketozole®, Nizoral®, Xolegel®)
- lamotrigine (Lamictal®)
- methadone hydrochloride (Dolphine hydrochloride, Methadose®)
- nicardipine (Cardene®)
- nifedipine (Adalat CC®, Afeditab CR®, Procardia®)
- phenytoin (Dilantin®, Phenytek®)
- quetiapine (Seroquel®)
- quinidine (Quinidex®)
- rifabutin (Mycobutin®)
- rivaroxaban (Xarelto®)
- rosuvastatin (Crestor®)
- salmeterol (Serevent®) or salmeterol when taken in combination with fluticasone (Advair Diskus®, Advair HFA®)
- simeprevir (Olysio®)
- tadalafil (Adcirca®) for the treatment of pulmonary arterial hypertension
- trazodone (Oleptro®)
- valproate (Depakote®, Depakene®, Depacon®)
- voriconazole (Vfend®)
- warfarin (Coumadin®, Jantoven®)
KALETRA should not be administered once daily in combination with carbamazepine (Carbatrol®, Epitol®, Equetro®, Tegretol®), phenobarbital, or phenytoin (Dilantin®, Phenytek®).
Ask your doctor or pharmacist if you are not sure if your medicine is one that is listed above.
Know all the medicines that you take. Keep a list of them with you to show doctors and pharmacists when you get a new medicine.
How should I take KALETRA?
- Take KALETRA every day exactly as prescribed by your doctor.
- It is very important to set up a dosing schedule and follow it every day.
- Do not change your treatment or stop treatment without first talking with your doctor.
- KALETRA capsules must be taken with food.
- If you are taking both didanosine (Videx®) and
- Didanosine should be taken one hour before or two hours after KALETRA.
- Do not miss a dose of KALETRA. This could make the virus harder to treat. If you forget to take KALETRA, take the missed dose right away. If it is almost time for your next dose, do not take the missed dose. Instead, follow your regular dosing schedule by taking your next dose at its regular time. Do not take more than one dose of KALETRA at one time.
- If you take more than the prescribed dose of KALETRA, call your doctor or go to the nearest emergency room right away.
- If your child is prescribed KALETRA, tell your doctor if your child's weight changes.
- KALETRA should not be given one time each day in children. When giving KALETRA to your child, give KALETRA exactly as prescribed.
- When your KALETRA supply starts to run low, get more from your doctor or pharmacy. It is important not to run out of KALETRA. The amount of HIV-1 virus in your blood may increase if the medicine is stopped for even a short time. The virus may become resistant to KALETRA and become harder to treat.
What are the possible side effects of KALETRA?
KALETRA can cause serious side effects including:
- See “What is the most important information I should know about KALETRA?”
- Inflammation of the pancreas (pancreatitis). Some people who take KALETRA get inflammation of the pancreas which may be serious and cause death. You have a higher chance of getting pancreatitis if you have had it before. Tell your doctor if you have nausea, vomiting, or abdominal pain while taking KALETRA. These may be signs of pancreatitis.
- Liver problems. Liver problems, including death,
can happen in people who take KALETRA. Your doctor should do blood tests before
and during your treatment with KALETRA to check your liver function. Some
people with liver disease such as Hepatitis B and Hepatitis C who take KALETRA
may have worsening liver disease. Tell your doctor right away if you have any of
these signs and symptoms of liver problems:
- loss of appetite
- yellow skin and whites of eyes (jaundice)
- dark-colored urine
- pale colored stools
- itchy skin
- stomach area (abdominal) pain
- Diabetes and high blood sugar (hyperglycemia). Some people who take protease inhibitors including KALETRA can get high blood sugar, develop diabetes, or diabetes can get worse. Tell your doctor if you notice an increase in thirst or urinate often while taking KALETRA.
- Changes in your immune system (Immune Reconstitution Syndrome) can happen when you start taking HIV medicines. Your immune system may get stronger and begin to fight infections that have been hidden in your body for a long time. Call your doctor right away if you start having new symptoms after starting your HIV medicine.
- Increases in certain fat (triglycerides and cholesterol) levels in your blood. Large increases of triglycerides and cholesterol can be seen in blood test results of some people who take KALETRA. Your doctor should do blood tests to check your cholesterol and triglyceride levels before you start taking KALETRA and during your treatment.
- Changes in body fat. Changes in body fat in some people who take antiretroviral therapy. These changes may include increased amount of fat in the upper back and neck (“buffalo hump”), breast, and around the trunk. Loss of fat from the legs, arms and face may also happen. The cause and long-term health effects of these conditions are not known at this time.
- Increased bleeding for hemophiliacs. Some people with hemophilia have increased bleeding with protease inhibitors including KALETRA.
- Allergic reactions. Skin rashes, some of them severe, can occur in people who take KALETRA. Tell your healthcare provider if you had a rash when you took another medicine for your HIV-1 infection or if you notice any skin rash when you take KALETRA.
- Common side effects of KALETRA include:
- increased fats in blood (triglycerides or cholesterol)
Tell your doctor about any side effect that bothers you or that does not go away.
These are not all of the possible side effects of KALETRA. For more information, ask your doctor or pharmacist.
Call your doctor for medical advice about side effects. You may report side effects to FDA at 1800-FDA-1088.
How should I store KALETRA?
- Store KALETRA in a refrigerator, between 36°F to 46°F (2°C to 8°C). KALETRA that is kept refrigerated may be used until the expiration date printed on the label.
- KALETRA that is stored at room temperature less than 77°F (25°C) should be used within 2 months.
- Keep KALETRA away from heat.
- Throw away any medicine that is out of date or that you no longer need.
Keep KALETRA and all medicines out of the reach of children.
General information about KALETRA
Medicines are sometimes prescribed for purposes other than those listed in a Medication Guide. Do not use KALETRA for a condition for which it was not prescribed. Do not give KALETRA to other people, even if they have the same condition you have. It may harm them.
This Medication Guide summarizes the most important information about KALETRA. If you would like more information, talk with your doctor. You can ask your pharmacist or doctor for information about KALETRA that is written for health professionals. For more information about KALETRA call 1-800-633-9110 or go to www.KALETRA.com.
What are the ingredients in KALETRA?
Active ingredients: lopinavir and ritonavir
FD&C Yellow No. 6, gelatin, glycerin, oleic acid, polyoxyl 35 castor oil, propylene glycol, sorbitol special, titanium dioxide, and water.
This Medication Guide has been approved by the U.S. Food and Drug Administration.
Last reviewed on RxList: 7/15/2015
This monograph has been modified to include the generic and brand name in many instances.
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Report Problems to the Food and Drug Administration
You are encouraged to report negative side effects of prescription drugs to the FDA. Visit the FDA MedWatch website or call 1-800-FDA-1088.
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