NEVIRAPINE - nevirapine suspension 
Aurobindo Pharma Limited

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MEDICATION GUIDE

Nevirapine Oral Suspension, USP

(ne vir' a peen)


What is the most important information I should know about nevirapine oral suspension?

Nevirapine oral suspension can cause severe liver and skin problems that may lead to death. These problems can happen at any time during treatment, but your risk is higher during the first 18 weeks of treatment.

Nevirapine oral suspension can cause serious side effects, including:


•   Severe liver problems. Some people taking nevirapine oral suspension may develop severe liver problems that can lead to liver failure and the need for a liver transplant, or death. If you have liver problems, you may get a rash. 

        • Women have a higher risk of developing liver problems during treatment with nevirapine oral suspension than men.
        • People who have abnormal liver test results before starting nevirapine oral suspension and people with hepatitis B or C also have a greater risk of getting liver problems. 

      People who have higher CD4+ cell counts when they begin nevirapine oral suspension have a higher risk of liver problems, especially: 

        • Women with CD4+ counts higher than 250 cells/mm3. This group has the highest risk.
        •  Men with CD4+ counts higher than 400 cells/mm3.  

     Stop taking nevirapine oral suspension and call your doctor right away if you have any of the following symptoms of liver problems with or without a skin rash:  

        • dark (tea colored) urine
        • yellowing of your skin or whites of your eyes
        • light-colored bowel movements (stools)
        • fever
        • feeling sick to your stomach (nausea)
        • feel unwell or like you have the flu
        • pain or tenderness on your right side below your ribs
        • tiredness
        • loss of appetite 

• Severe skin reactions and rash. Some skin reactions and rashes may be severe, life-threatening, and in some people, may lead to death. Most severe skin reactions and rashes happen in the first 6 weeks of treatment with nevirapine oral suspension.

    • Women have a higher risk of developing a rash during treatment with nevirapine oral suspension than men. 

       Stop taking nevirapine oral suspension and call your doctor right away if you get a rash with any of the following symptoms:

            • blisters
            • red or inflamed eyes, like “pink eye” (conjunctivitis)
            • swelling of your face
            • feel unwell or like you have the flu
            • muscle or joint aches
            • mouth sores
            • fever
            • tiredness 

See “What are the possible side effects of nevirapine oral suspension?”  for more information about side effects.


What is nevirapine oral suspension?  

Nevirapine oral suspension is prescription HIV-1 medicines used with other HIV-1 medicines to treat HIV-1 (Human Immunodeficiency Virus 1) in adults and in children 15 days of age or older. HIV-1 is the virus that causes AIDS (Acquired Immune Deficiency Syndrome).  

Do not take nevirapine oral suspension:  

Before taking nevirapine oral suspension, tell your doctor about all your or your child’s medical conditions, including if you or your child: 

Pregnancy Registry: There is a pregnancy registry for women who take nevirapine oral suspension during pregnancy. The purpose of the 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.

Tell your doctor about all the medicines you take, including prescription and over-the-counter medicines, vitamins and herbal supplements. Especially tell your doctor if you take St. John’s wort. 

How should I take nevirapine oral suspension?   

Your doctor should start you with 1 dose each day to lower your chance of getting a serious rash. It is important that you only take 1 dose of nevirapine oral suspension each day for the first 14 days.

Switching from nevirapine oral suspension to nevirapine extended-release tablets: 

If you take nevirapine oral suspension:

What are the possible side effects of nevirapine oral suspension?


Nevirapine oral suspension may cause serious side effects, including:


See “What is the most important information I should know about nevirapine oral suspension?”

The most common side effect of nevirapine oral suspension is rash. 

Nevirapine oral suspension may cause decreased fertility in females. Talk to your doctor if you have concerns about fertility. 

These are not all the possible side effects of nevirapine oral suspension. 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 1-800-FDA-1088.


How should I store nevirapine oral suspension?  

Keep nevirapine oral suspension and all medicines out of the reach of children.


General information about the safe and effective use of nevirapine oral suspension.


Medicines are sometimes prescribed for purposes other than those listed in a Medication Guide. Do not use nevirapine oral suspension for a condition for which it was not prescribed. Do not give nevirapine oral suspension to other people, even if they have the same condition you have. It may harm them. You can ask your pharmacist or doctor for information about nevirapine oral suspension that is written for health professionals. 


What are the ingredients in nevirapine oral suspension?  

Active ingredient: nevirapine


Inactive ingredients: carbopol 974PNF, methylparaben, propylparaben, non crystallizing sorbitol solution, sucrose, propylene glycol, polysorbate 80, sodium hydroxide, and purified water.


For more information, call Aurobindo Pharma USA, Inc. at 1-866-850-2876.


This Medication Guide has been approved by the U.S. Food and Drug Administration.

Dispense with Medication Guide available at: www.aurobindousa.com/medication-guides  


Distributed by:
Aurobindo Pharma USA, Inc.
279 Princeton-Hightstown Road
East Windsor, NJ 08520

Manufactured by:
Aurobindo Pharma Limited
Hyderabad-500 032, India

Revised: 07/2022

Revised: 4/2024
Aurobindo Pharma Limited