Atripla Oral Tablet 600-200-300Mg Drug Medication Dosage Information
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Atripla: Oral tablet (600-200-300mg)

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Drug Image file DrugItem_8365.JPG
Atripla 600mg-200mg-300mg Tab
Bristol Myers Squibb and Gilead Sciences
Pill Identification: 123 

What is this Medicine?

EFAVIRENZ; EMTRICITABINE; TENOFOVIR (e fa VEER ens; em tri SIT uh bean; te NOE fo veer) is three antiretroviral medicines in one tablet. It is used with other medicines to treat HIV. This medicine is not a cure for HIV. It will not stop the spread of HIV to others.

CVS Pharmacy Patient Statistics for Atripla: Oral tablet(600-200-300mg)
Generic vs. Brand Name Usage*
*Brand contains same active ingredient but may not represent FDA-approved generic equivalent
Usage By Strength
In-Depth Information

Atripla 600mg-200mg-300mg Tablet

NDC: 155840101
  • Prescription Required
  • Not a Controlled Drug
    (CSA Schedule)
  • FDA Approved




FDA approved for the following conditions:
Human Immunodeficiency Virus (HIV) Infection

Storage Information
Dispense in original container or USP equivalent tight container
Store at 77 degrees F; excursions permitted to 59-86 degrees F
Atripla 600mg-200mg-300mg Tablet
Drug Image file DrugItem_8365.JPG
Bristol Myers Squibb and Gilead Sciences
Pill Identification: 123 
Shape: oblong
Color: pink

Reported Side Effects for Atripla 600mg-200mg-300mg Tablet

Low Blood Sugar Incidence:
<3.0%*
Severity: MODERATE
Onset: EARLY
Stevens-Johnson Syndrome Incidence:
0.1-2.2%*
Severity: SEVERE
Onset: DELAYED
Skin Necrosis Incidence:
0.1-2.2%*
Severity: SEVERE
Onset: EARLY
Exfoliative Dermatitis Incidence:
0.1-2.2%*
Severity: SEVERE
Onset: DELAYED
Erythema Multiforme Incidence:
0.1-2.2%*
Severity: SEVERE
Onset: DELAYED
Lyell'S Syndrome Incidence:
0.1-2.2%*
Severity: SEVERE
Onset: DELAYED
Mania Incidence:
0.2%*
Severity: MODERATE
Onset: EARLY
Paranoia Incidence:
0.4%*
Severity: MILD
Onset: EARLY
Psychosis Incidence:
0.4%*
Severity: MODERATE
Onset: EARLY
Thoughts Of Suicide Incidence:
0.7%*
Severity: SEVERE
Onset: DELAYED
Skin Ulcer Incidence:
0.8-1.1%*
Severity: MODERATE
Onset: DELAYED
Vesicular Rash Incidence:
0.8-1.1%*
Severity: MILD
Onset: DELAYED
Glycosuria Incidence:
>1.0%*
Severity: MODERATE
Onset: EARLY
Increased Blood Sugar Incidence:
1.0-3.0%*
Severity: MODERATE
Onset: DELAYED
Hallucinations Incidence:
1.2%*
Severity: MODERATE
Onset: EARLY
Broken Bones Incidence:
1.3%*
Severity: SEVERE
Onset: DELAYED
Elevated Hepatic Enzymes Incidence:
2.0-3.0%*
Severity: MODERATE
Onset: DELAYED
Vomiting Incidence:
2.0%*
Severity: MILD
Onset: EARLY
Decreased Appetite Incidence:
>2.0%*
Severity: MILD
Onset: DELAYED
Depression Incidence:
2.4-9.0%*
Severity: MODERATE
Onset: DELAYED
Birth Defect Incidence:
2.8-3.6%*
Severity: SEVERE
Onset: DELAYED
High Bilirubin Level Incidence:
>3.0%*
Severity: MODERATE
Onset: DELAYED
Low White Blood Cells Incidence:
3.0%*
Severity: MODERATE
Onset: DELAYED
Blood In The Urine Incidence:
3.0%*
Severity: MODERATE
Onset: DELAYED
High Triglycerides Incidence:
4.0%*
Severity: MODERATE
Onset: DELAYED
Rhinitis Incidence:
>5.0%*
Severity: MILD
Onset: EARLY
Joint Pain Incidence:
>5.0%*
Severity: MILD
Onset: DELAYED
Cough Incidence:
>5.0%*
Severity: MILD
Onset: DELAYED
Paresthesias Incidence:
>5.0%*
Severity: MILD
Onset: DELAYED
Nervousness Incidence:
5.0%*
Severity: MILD
Onset: DELAYED
Rash With Pustules Incidence:
>5.0%*
Severity: MILD
Onset: EARLY
Stomach Pain Incidence:
>5.0%*
Severity: MILD
Onset: EARLY
Upset Stomach Incidence:
>5.0%*
Severity: MILD
Onset: EARLY
Infection Incidence:
5.0-8.0%*
Severity: MILD
Onset: DELAYED
Sore Throat Incidence:
5.0%*
Severity: MILD
Onset: DELAYED
Nerve Pain Incidence:
>5.0%*
Severity: MODERATE
Onset: DELAYED
Inflamed Nerve Incidence:
>5.0%*
Severity: MODERATE
Onset: DELAYED
Fever Incidence:
>5.0%*
Severity: MILD
Onset: EARLY
Muscle Pain Incidence:
>5.0%*
Severity: MILD
Onset: EARLY
Back Pain Incidence:
>5.0%*
Severity: MILD
Onset: DELAYED
Inability To Sleep Incidence:
5.0-16.3%*
Severity: MILD
Onset: EARLY
Blistery Rash Incidence:
>5.0%*
Severity: MODERATE
Onset: EARLY
Headache Incidence:
6.0%*
Severity: MILD
Onset: EARLY
Nightmares Incidence:
6.2%*
Severity: MILD
Onset: EARLY
Drowsiness Incidence:
7.0%*
Severity: MILD
Onset: EARLY
Lightheadedness Incidence:
8.0-28.1%*
Severity: MILD
Onset: EARLY
High Amylase Levels Incidence:
8.0%*
Severity: MODERATE
Onset: DELAYED
Sinus Infection Incidence:
8.0%*
Severity: MILD
Onset: DELAYED
Decreased Thinking Incidence:
8.3%*
Severity: MODERATE
Onset: EARLY
Itching Incidence:
8.8-10.7%*
Severity: MILD
Onset: RAPID
Tired Incidence:
9.0%*
Severity: MILD
Onset: EARLY
Loose Stools Incidence:
9.0%*
Severity: MILD
Onset: EARLY
Upset Stomach Incidence:
9.0%*
Severity: MILD
Onset: EARLY
High Cholesterol Incidence:
22.0%*
Severity: MODERATE
Onset: DELAYED
Skin Rash Incidence:
26.0-32.0%*
Severity: MILD
Onset: EARLY
*This is an approximate aggregated range of reported side effects from clinical studies performed on this drug. Your experience with this drug may be different.
Daily Life Interactions for Atripla 600mg-200mg-300mg Tablet

Elements of your daily lifestyle may have an effect on the medications you are taking. Drug interactions can result in unwanted side effects, reduce the effectiveness of your medicine or possibly increase the action of a particular medicine.

Major Lifestyle Interaction
Alcohol and Atripla 600mg-200mg-300mg Tablet(Tenofovir Disoproxil Fumarate)
Alcohol and Tenofovir(Tenofovir Disoproxil Fumarate)
Do not take these drugs together without approval from your prescriber. Taking these drugs together may decrease the effectiveness of your HIV medicines. Notify your health care provider if you notice your medicines not working as well of you.
Moderate Lifestyle Interaction
Alcohol and Atripla 600mg-200mg-300mg Tablet(Efavirenz)
Alcohol and Efavirenz(Efavirenz)
Taking Efavirenz with alcohol-containing drinks can lead to increased side effects. You may experience more severe dizziness, drowsiness, difficulty sleeping or concentrating, and nightmares. Do not drive or operate machinery if you are drinking alcohol-containing beverages.
Moderate Lifestyle Interaction
Marijuana and Atripla 600mg-200mg-300mg Tablet(Efavirenz)
Marijuana and Non-nucleoside reverse transcriptase inhibitors(Efavirenz)
Although an interaction is possible, these drugs may be used together. In therory, side effects from Marijuana, Medical may get worse if you take Anti-retroviral non-nucleoside reverse transcriptase inhibitors (NNRTIs). However, the importance of this interaction is not known. Notify your health care provider if you notice increased fatigue, nausea, vomiting, or any other unusual effects.
Moderate Lifestyle Interaction
Marijuana and Atripla 600mg-200mg-300mg Tablet(Emtricitabine)
Marijuana and Nucleoside reverse transcriptase inhibitors(Emtricitabine)
Although an interaction is possible, these drugs may be used together. In therory, side effects from Marijuana, Medical may get worse if you take Anti-retroviral nucleoside reverse transcriptase inhibitors (NRTIs). However, the importance of this interaction is not known. Notify your health care provider if you notice increased fatigue, nausea, vomiting, or any other unusual effects.
Moderate Lifestyle Interaction
Grapefruit juice and Atripla 600mg-200mg-300mg Tablet(Tenofovir Disoproxil Fumarate)
Grapefruit juice and Tenofovir(Tenofovir Disoproxil Fumarate)
Although an interaction is possible, these drugs are sometimes used together. Side effects may increase if these drugs are taken together. If you notice any new or worsening side effects, contact your prescriber immediately.
Moderate Lifestyle Interaction
Marijuana and Atripla 600mg-200mg-300mg Tablet(Tenofovir Disoproxil Fumarate)
Marijuana and Nucleotide reverse transcriptase inhibitors(Tenofovir Disoproxil Fumarate)
Although an interaction is possible, these drugs may be used together. In therory, side effects from Marijuana, Medical may get worse if you take Anti-retroviral nucleotide reverse transcriptase inhibitors. However, the importance of this interaction is not known. Notify your health care provider if you notice increased fatigue, nausea, vomiting, or any other unusual effects.
Pregnancy & Lactation Information
FIRST Trimester

Class D - Adequate well-controlled or observational studies in pregnant women have demonstrated a risk to the fetus. However, the benefits of therapy may outweigh the potential risk. For example, the drug may be acceptable if needed in a life-threatening situation or serious disease for which safer drugs cannot be used or are ineffective.

SECOND Trimester

Class D - Adequate well-controlled or observational studies in pregnant women have demonstrated a risk to the fetus. However, the benefits of therapy may outweigh the potential risk. For example, the drug may be acceptable if needed in a life-threatening situation or serious disease for which safer drugs cannot be used or are ineffective.

THIRD Trimester

Class D - Adequate well-controlled or observational studies in pregnant women have demonstrated a risk to the fetus. However, the benefits of therapy may outweigh the potential risk. For example, the drug may be acceptable if needed in a life-threatening situation or serious disease for which safer drugs cannot be used or are ineffective.

Lactation

Avoid - This drug is known to cause harm to infants when taken by nursing mothers.


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