Note: This document contains side effect information about tofacitinib. Some dosage forms listed on this page may not apply to the brand name Xeljanz.
Summary
Common side effects of Xeljanz include: infection. Other side effects include: diarrhea and headache. Continue reading for a comprehensive list of adverse effects.
Applies to tofacitinib: oral solution, oral tablets.
Warning
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Serious Infections
- Serious, sometimes fatal infections including tuberculosis (pulmonary or extrapulmonary disease), bacterial and viral infections, invasive fungal infections (may be disseminated), and other opportunistic infections reported.1 3 4 5
- Carefully consider risks and benefits prior to initiating tofacitinib therapy in patients with chronic or recurring infections.1
- Evaluate patients for latent tuberculosis infection prior to and periodically during tofacitinib therapy; if indicated, initiate appropriate antimycobacterial regimen prior to initiating tofacitinib therapy.1
- Closely monitor patients for infection, including active tuberculosis in those with a negative test for latent tuberculosis, during and after treatment.1 If serious infection develops, interrupt tofacitinib until infection is controlled.1
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Mortality
- Higher overall mortality rate, including sudden cardiovascular death, reported with tofacitinib 5 or 10 mg twice daily compared with a TNF blocking agent in a postmarketing safety study in rheumatoid arthritis patients ≥50 years of age with ≥1 cardiovascular risk factor.1 27 Tofacitinib dosage of 10 mg twice daily (as conventional tablets or oral solution) or 22 mg once daily (as extended-release tablets) is not recommended for the treatment of rheumatoid arthritis, psoriatic arthritis, or ankylosing spondylitis.1
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Malignancies
- Lymphoma and other malignancies (excluding nonmelanoma skin cancer) reported at a higher rate with tofacitinib 5 or 10 mg twice daily compared with TNF blocking agents in patients with rheumatoid arthritis.1 Risk of lymphomas and lung cancers were also increased with tofacitinib 5 or 10 mg twice daily compared with TNF blocking agents; patients who are current or past smokers are at additional risk.1
- Increased incidence of Epstein Barr virus-associated lymphoproliferative disorder observed in renal allograft recipients receiving tofacitinib and concomitant immunosuppressive agents.1
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Major Adverse Cardiovascular Events
- Higher rate of major adverse cardiovascular events reported with tofacitinib 5 or 10 mg twice daily compared with TNF blocking agents in a postmarketing safety study in patients with rheumatoid arthritis ≥50 years of age with ≥1 cardiovascular risk factor.1 Patients who are current or past smokers are at additional risk.1
- Discontinue tofacitinib in patients who experience MI or stroke.1
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Thrombosis
- Thromboembolic events, (i.e., PE, DVT, arterial thrombosis), sometimes serious or fatal, reported in patients receiving tofacitinib or other Janus kinase inhibitors for inflammatory conditions.1
- Higher incidence of thromboembolic events reported with tofacitinib 10 mg twice daily compared with either tofacitinib 5 mg twice daily or a TNF blocking agent in a postmarketing safety study in rheumatoid arthritis patients ≥50 years of age with ≥1 cardiovascular risk factor.1 27
- Discontinue tofacitinib and promptly evaluate patient if symptoms of thrombosis occur.1 27
- In patients with ulcerative colitis, use tofacitinib at lowest effective dosage and for shortest duration needed to achieve and maintain response.1 27
Side effects include:
Rheumatoid arthritis patients receiving tofacitinib (the active ingredient contained in Xeljanz) 5 or 10 mg twice daily monotherapy or in combination with DMARDs (≥2%): Diarrhea, headache, nasopharyngitis, upper respiratory tract infection.
Psoriatic arthritis and ankylosing spondylitis: Adverse effects similar to those observed in patients with rheumatoid arthritis.
Ulcerative colitis (≥5%): Nasopharyngitis, elevated cholesterol concentrations, headache, upper respiratory tract infection, increased blood creatine kinase (CK, creatine phosphokinase, CPK) concentrations, rash, diarrhea, herpes zoster.
Polyarticular-course JIA: Adverse effects generally consistent with those reported in adults with rheumatoid arthritis.
For Healthcare Professionals
Applies to tofacitinib: oral solution, oral tablet, oral tablet extended release.
General
In rheumatoid arthritis clinical trials, the most common serious adverse reactions were serious infections; the most common serious infections included pneumonia, cellulitis, herpes zoster, urinary tract infection, diverticulitis, and appendicitis. In ulcerative colitis induction and maintenance trials, the most common serious adverse reaction was worsening of ulcerative colitis.[Ref]
Cardiovascular
Common (1% to 10%): Hypertension
Uncommon (0.1% to 1%): Venous thromboembolism (includes pulmonary embolism, deep vein thrombosis), myocardial infarction
Frequency not reported: Deep vein thrombosis, nonfatal myocardial infarction, fatal myocardial infarction, arterial thromboembolism, major adverse cardiovascular events (includes nonfatal myocardial infarction, nonfatal stroke, cardiovascular death [excluding fatal pulmonary embolism]), thrombosis (including pulmonary embolism, deep venous thrombosis, arterial thrombosis), decreased heart rate, prolonged PR interval
Dermatologic
Common (1% to 10%): Rash, acne
Uncommon (0.1% to 1%): Erythema, pruritus, cellulitis, herpes simplex
Frequency not reported: Multidermatomal herpes zoster, pilonidal cyst
Postmarketing reports: Angioedema, urticaria
Gastrointestinal
Common (1% to 10%): Diarrhea, abdominal pain, dyspepsia, vomiting, gastritis, nausea, constipation, gastroenteritis, upper abdominal pain, ulcerative colitis
Uncommon (0.1% to 1%): Diverticulitis, viral gastroenteritis, appendicitis
Frequency not reported: Esophageal candidiasis, worsening of ulcerative colitis, gastrointestinal perforation, gastrointestinal obstruction
Genitourinary
Common (1% to 10%): Urinary tract infection
Uncommon (0.1% to 1%): Pyelonephritis
Rare (0.01% to 0.1%): Urosepsis
Hematologic
Common (1% to 10%): Anemia, decreased absolute lymphocyte count
Uncommon (0.1% to 1%): Leukopenia, neutropenia, lymphopenia
Rare (0.01% to 0.1%): Decreased absolute neutrophil count
Frequency not reported: Lymphocytosis
Hepatic
Common (1% to 10%): Increased AST, increased ALT, increased GGT
Uncommon (0.1% to 1%): Hepatic steatosis, increased hepatic enzymes, increased transaminases, abnormal liver function test
Frequency not reported: Drug-induced liver injury, increased bilirubin
Postmarketing reports: Hepatitis B reactivation
Hypersensitivity
Postmarketing reports: Hypersensitivity/allergic reactions, drug hypersensitivity (e.g., angioedema, urticaria)
Metabolic
Common (1% to 10%): Hypercholesterolemia
Uncommon (0.1% to 1%): Dehydration, dyslipidemia, hyperlipidemia
Musculoskeletal
Common (1% to 10%): Rheumatoid arthritis, back pain, arthralgia, increased blood creatine phosphokinase
Uncommon (0.1% to 1%): Musculoskeletal pain, tendonitis, joint swelling, ligament sprain, muscle strain
Rare (0.01% to 0.1%): Necrotizing fasciitis, bacterial arthritis
Frequency not reported: Limb abscess, fractures
Nervous system
Common (1% to 10%): Headache, dizziness
Uncommon (0.1% to 1%): Paresthesia
Rare (0.01% to 0.1%): Tuberculosis of central nervous system, encephalitis, cryptococcal meningitis
Frequency not reported: Aseptic meningitis, epidural empyema (with sinusitis and subperiosteal abscess)
Oncologic
Common (1% to 10%): Epstein Barr Virus-associated posttransplant lymphoproliferative disorder
Uncommon (0.1% to 1%): Lung cancer, nonmelanoma skin cancer (includes basal cell carcinoma, squamous cell carcinoma)
Rare (0.01% to 0.1%): Lymphoma
Frequency not reported: Solid cancers, malignancies (including solid cancers, lymphomas, nonmelanoma skin cancer, lung cancer, breast cancer, gastric cancer, colorectal cancer, renal cell cancer, prostate cancer, malignant melanoma), basal cell carcinoma, cutaneous squamous cell carcinoma, breast cancer, melanoma, prostate cancer, pancreatic cancer
Other
Very common (10% or more): Infections (up to 49.4%)
Common (1% to 10%): Pyrexia, fatigue, peripheral edema, herpes zoster, increased weight, fall, increased cholesterol levels (includes hypercholesterolemia, hyperlipidemia, increased blood cholesterol, dyslipidemia, increased blood triglycerides, increased low-density lipoprotein [LDL], abnormal LDL, increased lipids), increased blood cholesterol, serious infections
Uncommon (0.1% to 1%): Tuberculosis, viral infection, increased LDL
Rare (0.01% to 0.1%): Sepsis, disseminated tuberculosis, bacteremia, staphylococcal bacteremia, atypical mycobacterial infection, CMV infection, Mycobacterium avium complex infection
Frequency not reported: Opportunistic infections, other mycobacterial infections, cryptococcus, histoplasmosis, BK virus infection, listeriosis, increased lipid parameters (total cholesterol, LDL cholesterol, high-density lipoprotein [HDL] cholesterol, triglycerides), increased LDL cholesterol, increased HDL cholesterol, septic shock, opportunistic herpes zoster infections (including meningoencephalitis, ophthalmologic, disseminated cutaneous), viral reactivation (including herpes virus reactivation [e.g., herpes zoster]), all-cause mortality (including sudden cardiovascular death), deaths associated with infection, deaths associated with cardiovascular events, deaths associated with malignancies, deaths associated with other causes (excluding infections, cardiovascular events, malignancies), dissemination of the vaccine strain of varicella zoster virus
A patient had dissemination of the vaccine strain of varicella zoster virus, 16 days after vaccination with live attenuated virus vaccine and 2 days after starting therapy with 5 mg twice a day; the patient was varicella virus naive, as shown by no history of varicella infection and no anti-varicella antibodies at baseline. This drug was discontinued and the patient recovered after treatment with standard doses of antiviral therapy.
Psychiatric
Uncommon (0.1% to 1%): Insomnia
Renal
Uncommon (0.1% to 1%): Increased blood creatinine
Frequency not reported: Escherichia pyelonephritis
Respiratory
Very common (10% or more): Nasopharyngitis (up to 18.2%)
Common (1% to 10%): Pneumonia, influenza, sinusitis, pharyngitis, upper respiratory tract infections, bronchitis, cough, viral upper respiratory tract infection
Uncommon (0.1% to 1%): Dyspnea, sinus congestion
Rare (0.01% to 0.1%): Pneumocystis jirovecii pneumonia, pneumococcal pneumonia, bacterial pneumonia
Frequency not reported: Pulmonary embolism, interstitial lung disease