Medically reviewed by Drugs.com. Last updated on Mar 1, 2020.
(ve doe LIZ ue mab)
Excipient information presented when available (limited, particularly for generics); consult specific product labeling.
Solution Reconstituted, Intravenous [preservative free]:
Entyvio: 300 mg (1 ea) [contains polysorbate 80]
Brand Names: U.S.
- Gastrointestinal Agent, Miscellaneous
- Monoclonal Antibody
- Monoclonal Antibody, Selective Adhesion-Molecule Inhibitor
Vedolizumab is a humanized monoclonal antibody that binds to the alpha4beta7 integrin and blocks the interaction of alpha4beta7 integrin with mucosal addressin cell adhesion molecule-1 (MAdCAM-1) and inhibits the migration of memory T-lymphocytes across the endothelium into inflamed gastrointestinal parenchymal tissue. The interaction of the alpha4beta7 integrin with MAdCAM-1 has been implicated as an important contributor to the chronic inflammation that is a hallmark of ulcerative colitis and Crohn disease.
Vd: 5 L
25 days (serum, at 300 mg dosage)
Use: Labeled Indications
Crohn disease: Treatment of Crohn disease in adults.
Ulcerative colitis: Treatment of ulcerative colitis in adults.
Serious or severe hypersensitivity to vedolizumab or any component of the formulation
Canadian labeling: Additional contraindications (not in US labeling): Patients with active severe infections or opportunistic infections.
Note: Prior to initiating treatment, all patients should be brought up to date with all immunizations according to current immunization guidelines.
Crohn disease or ulcerative colitis: IV: 300 mg at 0, 2, and 6 weeks and then every 8 weeks thereafter. Discontinue therapy in patients who show no evidence of therapeutic benefit by week 14.
Refer to adult dosing.
Reconstitute with 4.8 mL of room temperature SWFI (final concentration of 60 mg/mL) using a syringe with a 21- to 25-gauge needle; direct stream of SWFI to glass wall of vial to avoid excessive foaming. Gently swirl vial for at least 15 seconds; do not vigorously shake or invert. Allow the solution to sit for up to 20 minutes at room temperature to allow for reconstitution and for any foam to settle; the vial can be swirled and inspected for dissolution during this time. If not fully dissolved after 20 minutes, allow another 10 minutes for dissolution. Do not use the vial if the drug product is not dissolved within 30 minutes. Solution should be clear or opalescent, colorless to light brownish yellow and free of visible particulates. Do not administer reconstituted solution showing uncharacteristic color or containing particulates.
Prior to withdrawing the reconstituted vedolizumab solution from the vial for dilution, gently invert vial 3 times. Add the 5 mL (300 mg) of reconstituted vedolizumab solution to 250 mL of sterile sodium chloride 0.9% or LR and gently mix the infusion bag. Once reconstituted and diluted, use the infusion solution as soon as possible.
IV: Infuse over 30 minutes. Do not administer by IV push or bolus. Following infusion, flush with 30 mL of sterile 0.9% sodium chloride injection or LR. Observe patients during infusion (until complete) and monitor for hypersensitivity reactions; discontinue if a reaction occurs.
Refrigerate unopened vials at 2°C to 8°C (36ºF to 46ºF). Retain in original package to protect from light.
Vials reconstituted with SWFI and solutions diluted for infusion in NS or LR may be stored as follows:
(2°C to 8°C [36ºF to 46ºF])
(20°C to 25°C [68ºF to 77ºF])
aThis time assumes the reconstituted solution is immediately diluted in NS or LR and held in the infusion bag only. Any time that the reconstituted solution was held in vial should be subtracted from the time the solution may be held in the infusion bag.
bThis period may include up to 12 hours at room temperature (20°C to 25°C [68ºF to 77ºF]).
cThe combined storage time of reconstituted solution in the vial and the diluted solution in the infusion bag with NS is a total of 12 hours at room temperature (20°C to 25°C [68ºF to 77ºF]) or 24 hours refrigerated (2°C to 8°C [36ºF to 46ºF]). This combined storage time may include up to 8 hours of the reconstituted solution in the vial at 2°C to 8°C (36ºF to 46ºF). Avoid freezing.
dThe combined storage time of reconstituted solution in the vial and the diluted solution in the infusion bag with LR is a total of 6 hours refrigerated (2°C to 8°C [36ºF to 46ºF]). Avoid freezing.
Vials reconstituted with SWFI
Use immediately after reconstitution
Diluted solution in NS
24 hoursa, b, c
12 hoursa, c
Diluted solution in LR
6 hoursa, d
Use immediately after dilution
Anti-TNF Agents: May enhance the adverse/toxic effect of Vedolizumab. Avoid combination
Baricitinib: Immunosuppressants may enhance the immunosuppressive effect of Baricitinib. Management: Use of baricitinib in combination with potent immunosuppressants such as azathioprine or cyclosporine is not recommended. Concurrent use with antirheumatic doses of methotrexate or nonbiologic disease modifying antirheumatic drugs (DMARDs) is permitted. Consider therapy modification
BCG (Intravesical): Immunosuppressants may diminish the therapeutic effect of BCG (Intravesical). Avoid combination
Cladribine: May enhance the immunosuppressive effect of Immunosuppressants. Avoid combination
Coccidioides immitis Skin Test: Immunosuppressants may diminish the diagnostic effect of Coccidioides immitis Skin Test. Monitor therapy
Denosumab: May enhance the adverse/toxic effect of Immunosuppressants. Specifically, the risk for serious infections may be increased. Monitor therapy
Echinacea: May diminish the therapeutic effect of Immunosuppressants. Management: Consider avoiding Echinacea in patients receiving therapeutic immunosuppressants. If coadministered, monitor for reduced efficacy of the immunosuppressant during concomitant use. Consider therapy modification
Fingolimod: Immunosuppressants may enhance the immunosuppressive effect of Fingolimod. Management: Avoid the concomitant use of fingolimod and other immunosuppressants when possible. If combined, monitor patients closely for additive immunosuppressant effects (eg, infections). Consider therapy modification
Inebilizumab: May enhance the immunosuppressive effect of Immunosuppressants. Monitor therapy
Leflunomide: Immunosuppressants may enhance the adverse/toxic effect of Leflunomide. Specifically, the risk for hematologic toxicity such as pancytopenia, agranulocytosis, and/or thrombocytopenia may be increased. Management: Consider not using a leflunomide loading dose in patients receiving other immunosuppressants. Patients receiving both leflunomide and another immunosuppressant should be monitored for bone marrow suppression at least monthly. Consider therapy modification
Natalizumab: Vedolizumab may enhance the adverse/toxic effect of Natalizumab. Avoid combination
Nivolumab: Immunosuppressants may diminish the therapeutic effect of Nivolumab. Management: Avoid use of immunosuppressants (including systemic corticosteroids) prior to initiation of nivolumab. Use of immunosuppressants after administration of nivolumab (eg, for immune-related toxicity) is unlikely to affect nivolumab efficacy. Consider therapy modification
Ocrelizumab: May enhance the immunosuppressive effect of Immunosuppressants. Monitor therapy
Ozanimod: Immunosuppressants may enhance the immunosuppressive effect of Ozanimod. Monitor therapy
Pidotimod: Immunosuppressants may diminish the therapeutic effect of Pidotimod. Monitor therapy
Pimecrolimus: May enhance the adverse/toxic effect of Immunosuppressants. Avoid combination
Roflumilast: May enhance the immunosuppressive effect of Immunosuppressants. Management: Consider avoiding concomitant use of roflumilast and immunosuppressants as recommended by the Canadian product monograph. Inhaled or short-term corticosteroids are unlikely to be problematic. Consider therapy modification
Siponimod: Immunosuppressants may enhance the immunosuppressive effect of Siponimod. Monitor therapy
Sipuleucel-T: Immunosuppressants may diminish the therapeutic effect of Sipuleucel-T. Management: Evaluate patients to see if it is medically appropriate to reduce or discontinue therapy with immunosuppressants prior to initiating sipuleucel-T therapy. Consider therapy modification
Smallpox and Monkeypox Vaccine (Live): Immunosuppressants may diminish the therapeutic effect of Smallpox and Monkeypox Vaccine (Live). Monitor therapy
Tacrolimus (Topical): May enhance the adverse/toxic effect of Immunosuppressants. Avoid combination
Talimogene Laherparepvec: Immunosuppressants may enhance the adverse/toxic effect of Talimogene Laherparepvec. Specifically, the risk for disseminated herpetic infection may be increased. Avoid combination
Tertomotide: Immunosuppressants may diminish the therapeutic effect of Tertomotide. Monitor therapy
Tofacitinib: Immunosuppressants may enhance the immunosuppressive effect of Tofacitinib. Management: Concurrent use with antirheumatic doses of methotrexate or nonbiologic disease modifying antirheumatic drugs (DMARDs) is permitted, and this warning seems particularly focused on more potent immunosuppressants. Consider therapy modification
Travelers' Diarrhea and Cholera Vaccine: Vedolizumab may diminish the therapeutic effect of Travelers' Diarrhea and Cholera Vaccine. Management: Administer travelers' diarrhea and cholera vaccine prior to initiation of therapy with vedolizumab. Consider therapy modification
Upadacitinib: Immunosuppressants may enhance the immunosuppressive effect of Upadacitinib. Management: Concomitant use of upadacitinib with potent immunosuppressants is not recommended. Avoid combination
Vaccines (Inactivated): Immunosuppressants may diminish the therapeutic effect of Vaccines (Inactivated). Management: Complete all age-appropriate vaccinations at least 2 weeks prior to starting an immunosuppressant. If vaccinated less than 2 weeks before starting or during immunosuppressant therapy, revaccinate at least 3 months after immunosuppressant discontinuation. Consider therapy modification
Vaccines (Live): Immunosuppressants may enhance the adverse/toxic effect of Vaccines (Live). Immunosuppressants may diminish the therapeutic effect of Vaccines (Live). Management: Avoid use of live organism vaccines with immunosuppressants; live-attenuated vaccines should not be given for at least 3 months after immunosuppressants. Avoid combination
The following adverse drug reactions and incidences are derived from product labeling unless otherwise specified.
Immunologic: Antibody development (4% to 13%; neutralizing: 2%)
Nervous system: Headache (12%)
Neuromuscular & skeletal: Arthralgia (12%)
Respiratory: Nasopharyngitis (13%)
1% to 10%:
Dermatologic: Pruritus (3%), skin rash (3%)
Gastrointestinal: Nausea (9%)
Hepatic: Increased serum alanine aminotransferase (≥3 x ULN: <2%), increased serum aspartate aminotransferase (≥3 x ULN: <2%)
Infection: Influenza (4%)
Nervous system: Fatigue (6%)
Neuromuscular & skeletal: Back pain (4%), limb pain (3%)
Respiratory: Bronchitis (4%), cough (5%), oropharyngeal pain (3%), sinusitis (3%), upper respiratory tract infection (7%)
Miscellaneous: Fever (9%), infusion related reaction (4%)
Frequency not defined: Hematologic & oncologic: Malignant neoplasm (excluding dysplasia and basal cell carcinoma)
Hepatic: Hepatitis, increased serum bilirubin, increased serum transaminases
Hypersensitivity: Anaphylaxis, bronchospasm, hypersensitivity reaction
Infection: Infection (including anal abscess, sepsis, tuberculosis, salmonella sepsis, meningitis due to Listeria monocytogenes, giardiasis, cytomegalovirus disease [colitis])
Nervous system: Progressive multifocal leukoencephalopathy
Concerns related to adverse effects:
• Hypersensitivity/infusion-related reactions: Hypersensitivity and infusion-related reactions have been reported including anaphylaxis, dyspnea, bronchospasm, urticaria, flushing, rash, and increased BP and heart rate. Reactions may occur with the first or subsequent infusions; onset may vary from during the infusion or up to several hours post-infusion. If anaphylaxis or other serious infusion-related or hypersensitivity reactions occur, discontinue administration immediately and initiate appropriate treatment.
• Infections: Use may be associated with an increased risk for developing infections; most commonly reported infections included upper respiratory and nasal mucosa. Serious infections have also been reported in patients treated, including anal abscess, sepsis (some fatal), tuberculosis, salmonella sepsis, Listeria meningitis, giardiasis, and cytomegaloviral colitis. Therapy is not recommended in patients with uncontrolled, active, severe infections. If a patient develops a serious infection, consider discontinuing therapy. Use with caution in patients with a history of recurring severe infections. Screening for tuberculosis should be considered.
• Liver injury: Elevations of transaminase and/or bilirubin have been reported in patients receiving vedolizumab. Discontinue therapy in patients with jaundice or other evidence of significant liver injury such as fatigue, anorexia, right upper abdominal discomfort, or dark urine.
• Progressive multifocal leukoencephalopathy: Progressive multifocal leukoencephalopathy (PML), a rare and often fatal opportunistic infection of the CNS caused by the John Cunningham virus, has been reported with integrin receptor antagonists, including vedolizumab. Monitor patients for any new onset or worsening of neurological signs and symptoms including progressive weakness on one side of the body or clumsiness of limbs, disturbance of vision, and changes in thinking, memory, and orientation leading to confusion and personality changes. Symptoms may progress over days to weeks and can lead to death or severe disability in weeks to months. If PML is suspected, withhold therapy and refer to a neurologist; if confirmed, discontinue therapy permanently.
• Immunizations: Patients should be brought up to date with all immunizations according to immunization guidelines before initiating therapy. Live vaccines should not be given concurrently unless the benefits outweigh the risks; there are no data on the secondary transmission of infection by live vaccines with vedolizumab. Non-live vaccines may be given concurrently.
Observe patients during infusion (until complete) and monitor for hypersensitivity reactions; LFTs; tuberculosis screening according to local practice; signs/symptoms of infection; any new onset or worsening of neurological signs and symptoms
Treatment algorithms are available for use of biologics in female patients with Crohn disease who are planning a pregnancy (Weizman 2019). When treatment for inflammatory bowel disease is needed, serum levels of biologic therapy should be optimized prior to conception (Mahadevan 2019).
Vedolizumab crosses the placenta (Mahadevan 2016).
Vedolizumab is a humanized monoclonal antibody (IgG1). Placental transfer of human IgG is dependent upon the IgG subclass, maternal serum concentrations, birth weight, and gestational age, generally increasing as pregnancy progresses. The lowest exposure would be expected during the period of organogenesis (Palmeira 2012; Pentsuk 2009).
Information related to the use of vedolizumab in pregnancy is available (Bar-Gil Shitrit 2019; Julsgaard 2017; Mahadevan 2017; Moens 2019; Sheridan 2017). Based on available data, an increased risk of adverse maternal or fetal effects has not been observed following vedolizumab exposure in pregnancy.
The safety of administering live vaccines to infants exposed to vedolizumab in utero is not known. Vaccination with live vaccines (eg, rotavirus vaccine) should be avoided for the first 6 months of life if exposure to a biologic agent occurs during the third trimester of pregnancy (eg, >27 weeks' gestation) (Mahadevan 2019).
Inflammatory bowel disease is associated with adverse pregnancy outcomes including an increased risk of miscarriage, premature delivery, delivery of a low birth weight infant, and poor maternal weight gain. Management of maternal disease should be optimized prior to pregnancy. Treatment decreases disease flares, disease activity, and the incidence of adverse pregnancy outcomes (Mahadevan 2019).
When treatment for inflammatory bowel disease is needed in pregnant women, appropriate biologic therapy can be continued without interruption. Serum levels should be evaluated prior to conception and optimized to avoid subtherapeutic concentrations or high levels which may increase placental transfer. Dosing can be adjusted so delivery occurs at the lowest serum concentration. For vedolizumab, the final injection can be given 6 to 10 weeks prior to the estimated date of delivery (4 to 5 weeks before delivery if every-4-week dosing), then continued 48 hours' postpartum (Mahadevan 2019).
Data collection to monitor pregnancy and infant outcomes following exposure to vedolizumab is ongoing. Health care providers are encouraged to enroll women exposed to vedolizumab during pregnancy in a pregnancy exposure registry. Information about the registry can be obtained by calling 1-877-825-3327.
What is this drug used for?
• It is used to treat Crohn disease.
• It is used to treat ulcerative colitis.
• It may be given to you for other reasons. Talk with the doctor.
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:
• Back pain
• Common cold symptoms
• Joint pain
• Stuffy nose
• Sore throat
• Painful extremities
• Loss of strength and energy
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:
• Infusion reaction
• Liver problems like dark urine, feeling tired, lack of appetite, nausea, abdominal pain, light-colored stools, vomiting, or yellow skin or eyes.
• Shortness of breath
• Passing out
• Vision changes
• Fast heartbeat
• Abnormal heartbeat
• Severe headache
• Progressive multifocal leukoencephalopathy like confusion, depression, trouble with memory, behavioral changes, change in strength on one side, trouble speaking, change in balance, or vision changes.
• Signs of an allergic reaction, like rash; hives; itching; red, swollen, blistered, or peeling skin with or without fever; wheezing; tightness in the chest or throat; trouble breathing, swallowing, or talking; unusual hoarseness; or swelling of the mouth, face, lips, tongue, or throat.
Note: This is not a comprehensive list of all side effects. Talk to your doctor if you have questions.
Consumer Information Use and Disclaimer: This information should not be used to decide whether or not to take this medicine or any other medicine. Only the healthcare provider has the knowledge and training to decide which medicines are right for a specific patient. This information does not endorse any medicine as safe, effective, or approved for treating any patient or health condition. This is only a limited summary of general information about the medicine’s uses from the patient education leaflet and is not intended to be comprehensive. This limited summary does NOT include all information available about the possible uses, directions, warnings, precautions, interactions, adverse effects, or risks that may apply to this medicine. This information is not intended to provide medical advice, diagnosis or treatment and does not replace information you receive from the healthcare provider. For a more detailed summary of information about the risks and benefits of using this medicine, please speak with your healthcare provider and review the entire patient education leaflet.
Frequently asked questions
- Is Entyvio an immunosuppressant or a biologic?
- How much does Entyvio cost per month?
- Can I take antibiotics while on Entyvio?
- How long has Entyvio been on the market?
- Does Medicaid cover Entyvio?
More about vedolizumab
- Side Effects
- During Pregnancy or Breastfeeding
- Dosage Information
- Drug Interactions
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- Drug class: selective immunosuppressants
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