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Vitekta Side Effects

Generic name: elvitegravir

Medically reviewed by Drugs.com. Last updated on Nov 11, 2023.

Note: This document contains side effect information about elvitegravir. Some dosage forms listed on this page may not apply to the brand name Vitekta.

Applies to elvitegravir: oral tablet.

Serious side effects of Vitekta

WARNING/CAUTION: Even though it may be rare, some people may have very bad and sometimes deadly side effects when taking a drug. Tell your doctor or get medical help right away if you have any of the following signs or symptoms that may be related to a very bad side effect:

Other side effects of Vitekta

All drugs may cause side effects. However, many people have no side effects or only have minor side effects. Call your doctor or get medical help if any of these side effects or any other side effects bother you or do not go away:

These are not all of the side effects that may occur. If you have questions about side effects, call your doctor. Call your doctor for medical advice about side effects.

You may report side effects to the FDA at 1-800-332-1088. You may also report side effects at https://www.fda.gov/medwatch.

For Healthcare Professionals

Applies to elvitegravir: oral tablet.

Gastrointestinal

Very common (10% or more): Increased lipase (14%), diarrhea (up to 13%)

Common (1% to 10%): Abdominal pain, vomiting, nausea, increased serum amylase

Uncommon (0.1% to 1%): Dyspepsia, abdominal distension, flatulence[Ref]

Increased serum amylase (greater than 2 times the upper limit of normal [2 x ULN]) has been reported in 6% of patients.

If serum amylase was greater than 1.5 x ULN, lipase was also measured. Increased lipase (grades 3 to 4) has been reported in 14% of patients.[Ref]

Hepatic

Increased total bilirubin (greater than 2.5 x ULN), GGT (greater than 5 x ULN), ALT (greater than 5 x ULN), and AST (greater than 5 x ULN) have been reported in 6%, 3%, 2%, and 2% of patients, respectively.[Ref]

Common (1% to 10%): Increased total bilirubin, increased ALT, increased AST[Ref]

Musculoskeletal

Common (1% to 10%): Increased creatine kinase, back pain, arthralgia, pain in extremity

Frequency not reported: Osteonecrosis[Ref]

Increased creatine kinase (at least 10 x ULN) has been reported in 6% of patients.[Ref]

Genitourinary

Hematuria (greater than 75 RBC/high power field) and urine glucose (4+) have been reported in 6% and 4% of patients, respectively.[Ref]

Common (1% to 10%): Hematuria, urine glucose[Ref]

Metabolic

Increased total cholesterol (greater than 300 mg/dL), increased total triglycerides (greater than 750 mg/dL), and hyperglycemia (greater than 250 mg/dL) have each been reported in 5% of patients.[Ref]

Common (1% to 10%): Increased total cholesterol, increased total triglycerides, hyperglycemia[Ref]

Nervous system

Common (1% to 10%): Headache

Uncommon (0.1% to 1%): Dizziness, paresthesia, somnolence, dysgeusia[Ref]

Hematologic

Decreased neutrophils (less than 750/mm3) has been reported in 3% of patients.[Ref]

Common (1% to 10%): Decreased neutrophils[Ref]

Psychiatric

Common (1% to 10%): Depression

Uncommon (0.1% to 1%): Suicidal ideation, suicide attempt, insomnia[Ref]

Suicidal ideation and suicide attempt were reported in patients with history of depression or psychiatric illness.[Ref]

Dermatologic

Common (1% to 10%): Rash[Ref]

Other

Common (1% to 10%): Fatigue[Ref]

Immunologic

Frequency not reported: Autoimmune disorders (e.g., Graves' disease)[Ref]

Frequently asked questions

References

1. Cerner Multum, Inc. UK Summary of Product Characteristics.

2. EMEA. European Medicines Agency. EPARs. European Union Public Assessment Reports. http://www.ema.europa.eu/ema/index.jsp?curl=pages/includes/medicines/medicines_landingpage.jsp&mid 2007.

3. Cerner Multum, Inc. Australian Product Information.

4. Product Information. Vitekta (elvitegravir). Gilead Sciences. 2014.

Further information

Always consult your healthcare provider to ensure the information displayed on this page applies to your personal circumstances.

Some side effects may not be reported. You may report them to the FDA.