(ter-i-floo-noe-mide) ,


(trade name)


Therapeutic: anti multiple sclerosis agents
Pharmacologic: immune response modifiers
Pregnancy Category: X


Management of relapsing forms of multiple sclerosis (MS).


Inhibits an enzyme required for pyrimidine synthesis; has antiproliferative and anti-inflammatory effects.

Therapeutic effects

↓ incidence and severity of relapses in MS, with a decrease in disability progression.


Absorption: Well absorbed following oral administration.
Distribution: Unknown.
Protein Binding: >99%.
Metabolism and Excretion: Eliminated via biliary excretion of unchanged drug with renal excretion of metabolites (37.5 in feces and 22.6% in urine), some metabolism occurs.
Half-life: 18–19 days.

Time/action profile (decrease in disability progression)

PO3–6 mounknownunknown


Contraindicated in: Severe hepatic impairment;Concurrent leflunomide treatment;Live virus vaccinations;Active acute or chronic infection;Severe immunodeficiency, bone marrow disease or severe uncontrolled infection; Lactation: Discontinue teriflunomide or discontinue breast feeding; Obstetric: Pregnancy or woman with childbearing potential using unreliable contraception (may cause fetal harm).
Use Cautiously in: Pre-existing liver disease;Severe immunodeficiency, bone marrow disease or severe uncontrolled infection;Hypertension (treat appropriately prior); Geriatric: Age >60 yr, concurrent neurotoxic medications or diabetes mellitus (↑ risk of peripheral neuropathy); Obstetric: Women with child-bearing potential; Pediatric: Safe and effective use in children has not been established.

Adverse Reactions/Side Effects


  • hypertension


  • interstitial lung disease (rare) (life-threatening)


  • hepatotoxicity (life-threatening)
  • diarrhea (most frequent)
  • ↑ transaminases (most frequent)
  • nausea (most frequent)


  • acute renal failure (urate nephropathy)


  • severe skin reactions including stevens-johnson syndrome and toxic epidermal necrolysis
  • alopecia (most frequent)

Fluid and Electrolyte

  • hyperkalemia
  • hypophosphatemia


  • leukopenia
  • neutropenia
  • thrombocytopenia


  • paresthesia (most frequent)
  • peripheral neuropathy


  • atypical infections, including Latent tuberculosis (life-threatening)
  • influenza (most frequent)


Drug-Drug interaction

May ↑ levels and effects of drugs metabolized by the CYP2C8 enzyme system including paclitaxel, pioglitazone, repaglinide, and rosiglitazone.May ↓ levels and effectiveness of drugs metabolized by the CYP1A2 enzyme system including alosetron, duloxetine, thoephylline, and tizanidine.May ↓ response to and ↑ risk of adverse reactions from live vaccines (avoid live vaccinations and consider long half-life of teriflunomide before administering).May ↑ levels and effects of ethinylestradiol and levonorgestrel.May ↑ risk of bleeding with warfarin.↑ risk of additive immunosuppression with other immunosuppressants or antineoplastics (consider long half-life of teriflunomide).Levels and effects may be ↑ by breast cancer resistant protein (BCRP) inhibitors including cyclosporine, eltrombopag, and gefitinib.May alter response to warfarin.May ↑ risk of adverse reactions and ↓ antibody response tolive virus vaccines.


Oral (Adults) 7 or 14 mg once daily.


Film-coated tablets: 7 mg, 14 mg

Nursing implications

Nursing assessment

  • Assess BP before starting and periodically during therapy. Treat hypertension as needed.
  • Lab Test Considerations: Monitor liver function tests (transaminases, bilirubin) within 6 months of starting therapy and monthly after teriflunomide therapy begins. Do not administer if ALT >2 × upper limit of normal. Consider discontinuing therapy if serum transaminase ↑ >3 × upper limit of normal is confirmed. Monitor serum transaminase and bilirubin in patients with symptoms of liver dysfunction. If liver injury is suspected, discontinue teriflunomide, begin accelerated elimination procedure, and monitor liver function tests weekly until normal.
    • Obtain a pregnancy test from female patients prior to beginning therapy.
    • Monitor CBC with platelet count within 6 months prior to starting and periodically during therapy based on signs and symptoms of infection. Mean decrease in WBC occurs during first 6 wks and remains low during therapy.
    • Monitor INR closely in patients taking warfarin, a decrease in warfarin peak may occur.

Potential Nursing Diagnoses

Impaired physical mobility (Indications)


  • Administer a tuberculin skin test prior to administration of teriflunomide. Patients with active latent TB should be treated for TB prior to therapy.
  • Oral: Administer once daily without regard to food.
  • Drug Elimination Procedure: Either of the following procedures is recommended to achieve nondetectable plasma levels <0.02 mg/L after stopping treatment with teriflunomide. 1) Administer cholestyramine 8 g 3 times daily (every 8 hrs) for 11 days. If cholestyramine 8 g is not well tolerated, cholestyramine 4 g 3 times/day can be used. or 2) Administration of 50 g oral activated charcoal powder every 12 hr for 11 days. (Days do not need to be consecutive unless rapid lowering of levels is desired.) Verify plasma levels <0.02 mg/L by 2 separate tests at least 14 days apart. Plasma levels may take up to 2 yr to reach nondetectable levels without drug elimination procedure.

Patient/Family Teaching

  • Instruct patient to take teriflunomide as directed. Advise patient to read Medication Guide before starting therapy and with each Rx refill in case of changes.
  • Advise patient to notify health care professional promptly if symptoms of liver problems (nausea, vomiting, stomach pain, loss of appetite, tiredness, skin or whites of eyes yellowing, dark urine), serious skin problems (redness or peeling), infection (fever, tiredness, body aches, chills, nausea, vomiting), or interstitial lung disease (cough, dyspnea, with or without fever) occur.
  • Instruct patient to notify health care professional if symptoms of peripheral neuropathy (numbness and tingling in hands and feet different from symptoms of MS), kidney problems (flank pain), high potassium level (nausea or racing heartbeat), or high BP occur.
  • Instruct patient to notify health care professional of all Rx or OTC medications, vitamins, or herbal products being taken and consult health care professional before taking any new medications.
  • Instruct patient to avoid vaccinations with live vaccines during and following therapy without consulting health care professional.
  • Discuss the possibility of hair loss with patient. Explore methods of coping.
  • Advise patient that teriflunomide is teratogenic. Effective birth control should be used during therapy and until blood levels of teriflunomide are low enough. If pregnancy is planned or suspected, or if breast feeding notify health care professional immediately, accelerated eliminated procedure may be used to decrease blood levels more rapidly. Male patients with female partner who plans to become pregnant may also use this method. If female partner does not plan to become pregnant, use effective birth control until blood levels are low enough; may require 2 years. Females of childbearing potential are recommended to undergo accelerated elimination procedure upon discontinuation of teriflunomide. Patients who become pregnant should be encouraged to enroll in the Aubagio Pregnancy Registry at 1-800-745-4447 to collect information about mother and baby's health.

Evaluation/Desired Outcomes

  • Decrease in the number of MS flares (relapses) and slowing of physical problems caused by MS.
Drug Guide, © 2015 Farlex and Partners
References in periodicals archive ?
Switzerland-based Novartis' human anti-CD20 monoclonal antibody, ofatumumab (OMB157), indicated superiority over Aubagio (teriflunomide) in two phase three trials in patients with relapsing forms of multiple sclerosis, it is reported today.
In both head-to-head studies, ofatumumab demonstrated superiority over Aubagio (teriflunomide) in patients with relapsing forms of multiple sclerosis (RMS)[1].
The companies said the ASCLEPIOS studies -- which evaluated the safety and efficacy of monthly subcutaneous atumumab 20mg versus Sanofi SA (NASDAQ: SNY)'s teriflunomide 14mg once-daily oral in adults with relapsing forms of multiple sclerosis -- met the primary and secondary endpoints.
From 2006 to 2016, there was a substantial drop in platform therapies in favor of newer therapies; decreases were seen in the market shares of brand-name glatiramers (from 36.7 to 32.2 percent), interferon beta-1a (30 [micro]g: 32.3 to 14.2 percent), interferon beta-1b (18.7 to 4.5 percent), and interferon beta-1a (8.8/22/44 [micro]g: 12.2 to 8.3 percent); increases were seen in fingolimod (to 7.9 percent), teriflunomide (to 9.0 percent), and dimethyl fumarate (to 19.2 percent).
Glenmark Pharmaceuticals Inc., USA has been granted final approval by the Food and Drug Administration for teriflunomide tablets, 7 mg and 14 mg, a generic version of Aubagio Tablets, 7 mg and 14 mg, from Sanofi-Aventis U.S.
The primary objective of the current analysis was to assess the efficacy and safety of two teriflunomide doses (7 mg and 14 mg) in the subgroup of Chinese patients with relapsing MS included in the TOWER study.
For the autoimmune diseases, the drugs and trade names are abatacept (Orencia), adalimumab (Humira), certolizumab pegol (Cimzia), etanercept (Enbrel), infliximab (Remicade), leflunomide (Arava), otezla (Apremilast), teriflunomide (Aubagio), tocilizumab (Actemra), tofacitinib (Xeljanz), and ustekinumab (Stelara).
IFN was used in 16 patients (53.40%) and other drugs (Glatiramer acetate, Fingolimod, Natalizumab, Teriflunomide) were used in 14 patients (46.60%) (Table 1).
ULTIMATE I and II are two independent Phase 3 clinical trials evaluating the safety and efficacy of ublituximab, the company's glycoengineered anti-CD20 monoclonal antibody, as compared to teriflunomide, in patients with relapsing forms of Multiple Sclerosis, or RMS.
Other drugs, such as fingolimod, teriflunomide, and dimethyl fumarate, have immunomodulatory functions and have been shown to inhibit C.