What are Some Possible Side Effects of ATRIPLA?
ATRIPLA may cause serious side effects
Do not stop taking ATRIPLA unless directed by your healthcare provider. See your healthcare provider regularly.
Contact your healthcare provider right away if you get the following side effects or conditions associated with ATRIPLA:
- Nausea, vomiting, unusual muscle pain, and/or weakness. These may be signs of a buildup of acid in the blood (lactic acidosis), which is a serious medical condition.
- Light-colored stools, dark-colored urine, and/or if your skin or the whites of your eyes turn yellow. These may be signs of serious liver problems.
- If you have HIV-1 and hepatitis B virus (HBV), your liver disease may suddenly get worse if you stop taking ATRIPLA.
Tell your healthcare provider if you:
- Are pregnant: Women should not become pregnant while taking ATRIPLA and for
12 weeks after stopping ATRIPLA. Serious birth defects have been seen in children of women treated during
pregnancy with one of the medicines in ATRIPLA. Women must use a reliable form of barrier
contraception, such as a condom or diaphragm, even if they also use other methods of birth control
while on ATRIPLA and for 12 weeks after stopping ATRIPLA.
- Are breastfeeding: Women with HIV should not breastfeed because they can pass HIV through
their milk to the baby. Also, ATRIPLA may pass through breast milk and cause serious harm to the
baby.
- Have liver problems, including hepatitis B or C virus infection.
- Have ever had seizures: Seizures have occurred in patients taking a component of ATRIPLA,
usually in those with a history of seizures. If you have ever had seizures, or take medicine for
seizures, your healthcare provider may want to switch you to another medicine or monitor you.
- Have ever had mental illness or use drugs or alcohol.
In addition, you should also contact your healthcare provider right away if you experience any of the following serious or common side effects:
Serious side effects associated with ATRIPLA:
- Severe depression, strange thoughts, or angry behavior have been reported
by a small number of patients. Some patients have had thoughts of suicide and a
few have actually committed suicide. These problems may occur more often in patients
who have had mental illness.
- Kidney problems (including decline or failure of kidney function). If you have had
kidney problems, or take other medicines that may cause kidney problems, your healthcare
provider should do regular blood tests. Symptoms that may be related to kidney problems
include a high volume of urine, thirst, muscle pain, and muscle weakness.
- Bone changes. Lab tests show changes in the bones of patients treated with tenofovir DF, a
component of ATRIPLA. Some HIV patients treated with tenofovir DF developed thinning of the
bones (osteopenia) which could lead to fractures. Also, bone pain and softening of the bone (which
may lead to fractures) may occur as a consequence of kidney problems. If you have had bone
problems in the past, your healthcare provider may want to check your bones.
Common side effects during treatment with ATRIPLA may include:
- Dizziness, headache, trouble sleeping, drowsiness, trouble concentrating, and/or unusual
dreams.These side effects tend to go away after taking ATRIPLA® (efavirenz
600 mg/ emtricitabine 200 mg/tenofovir DF 300 mg) for a few weeks. These symptoms may be more severe with the use of alcohol and/or mood-altering (street) drugs. If you are dizzy, have trouble concentrating, and/or are drowsy, avoid activities that may be dangerous, such as driving or operating machinery.
- Rash is a common side effect that usually goes away without any change in treatment, but may be serious in a small number of patients.
- Other common side effects include: tiredness, upset stomach, vomiting, gas, and diarrhea.
These side effects may be less bothersome if you take ATRIPLA at bedtime on an empty stomach. Most of these common side effects tend to go away after a few weeks. Tell your healthcare provider right away if these side effects continue, or if they bother you.
Other possible side effects:
- Changes in body fat have been seen in some people taking anti-HIV-1 medicines. These changes may include an increased amount of fat in the upper back and neck (“buffalo hump”), in the breasts, and around the trunk. Loss of fat from the legs, arms, and face may also happen. The cause and long-term health effects are not known.
- Skin discoloration (small spots or freckles) may also happen.
- If you notice any symptoms of infection, contact your healthcare provider right away.
- Additional side effects are inflammation of the pancreas, allergic reaction (including swelling of the
face, lips, tongue, or throat), shortness of breath, pain, stomach pain, weakness and indigestion.
Tell your healthcare provider right away if you notice any side effects while taking ATRIPLA. Also, contact your healthcare provider before stopping ATRIPLA because of side effects or any other reason.
ATRIPLA does not cure HIV-1 and has not been shown to prevent passing HIV-1 to others.
Ask your doctor if ATRIPLA is right for you, and see your healthcare provider regularly. Individual results may vary.
Please
click here for Important Safety Information, including information on
lactic acidosis,
serious liver problems, and
flare-ups of hepatitis B virus (HBV).