Leflunomida Jenson Pharmaceutical Services Uses

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What is Leflunomida Jenson Pharmaceutical Services?

Leflunomida Jenson Pharmaceutical Services affects the immune system and reduces swelling and inflammation in the body.

Leflunomida Jenson Pharmaceutical Services is used to treat the symptoms of rheumatoid arthritis. Leflunomida Jenson Pharmaceutical Services also helps reduce joint damage and improves physical functioning.

Leflunomida Jenson Pharmaceutical Services may also be used for other purposes not listed in this medication guide.

Leflunomida Jenson Pharmaceutical Services indications

An indication is a term used for the list of condition or symptom or illness for which the medicine is prescribed or used by the patient. For example, acetaminophen or paracetamol is used for fever by the patient, or the doctor prescribes it for a headache or body pains. Now fever, headache and body pains are the indications of paracetamol. A patient should be aware of the indications of medications used for common conditions because they can be taken over the counter in the pharmacy meaning without prescription by the Physician.
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Treatment of active rheumatoid arthritis (RA) in adults to reduce signs and symptoms, inhibit structural damage as evidence by X-ray erosions and joint space narrowing, and improve physical function.

Aspirin, nonsteroidal anti-inflammatory agents and/or low dose corticosteroids may be continued during treatment with Leflunomida Jenson Pharmaceutical Services. The combined use of Leflunomida Jenson Pharmaceutical Services with antimalarials, IM or oral gold, D-penicillamine, azathioprine or methotrexate has not been adequately studied.

How should I use Leflunomida Jenson Pharmaceutical Services?

Use Leflunomida Jenson Pharmaceutical Services as directed by your doctor. Check the label on the medicine for exact dosing instructions.

Ask your health care provider any questions you may have about how to use Leflunomida Jenson Pharmaceutical Services.

Uses of Leflunomida Jenson Pharmaceutical Services in details

There are specific as well as general uses of a drug or medicine. A medicine can be used to prevent a disease, treat a disease over a period or cure a disease. It can also be used to treat the particular symptom of the disease. The drug use depends on the form the patient takes it. It may be more useful in injection form or sometimes in tablet form. The drug can be used for a single troubling symptom or a life-threatening condition. While some medications can be stopped after few days, some drugs need to be continued for prolonged period to get the benefit from it.
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Use: Labeled Indications

Rheumatoid arthritis: Treatment of adults with active rheumatoid arthritis (RA).

Off Label Uses

BK virus (viremia or nephropathy; in kidney transplant recipients)

Data from a small retrospective study suggest Leflunomida Jenson Pharmaceutical Services may be of benefit as a replacement for mycophenolate in kidney transplant recipients with BK virus (viremia or nephropathy).

Leflunomida Jenson Pharmaceutical Services description

Leflunomida Jenson Pharmaceutical Services is a pyrimidine synthesis inhibitor belonging to the DMARD (disease-modifying antirheumatic drug) class of drugs, which are chemically and pharmacologically very heterogeneous. Leflunomida Jenson Pharmaceutical Services was approved by FDA and in many other countries (e.g., Canada, Europe) in 1999.

Leflunomida Jenson Pharmaceutical Services dosage

Leflunomida Jenson Pharmaceutical Services Dosage

Generic name: Leflunomida Jenson Pharmaceutical Services 10mg

Dosage form: tablet, film coated

The information at Drugs.com is not a substitute for medical advice. Always consult your doctor or pharmacist.

Recommended Dosage

The recommended dosage of Leflunomida Jenson Pharmaceutical Services is 20 mg once daily. Treatment may be initiated with or without a loading dose, depending upon the patient's risk of Leflunomida Jenson Pharmaceutical Services-associated hepatotoxicity and Leflunomida Jenson Pharmaceutical Services-associated myelosuppression. The loading dosage provides steady-state concentrations more rapidly.

The maximum recommended daily dosage is 20 mg once per day. Consider dosage reduction to 10 mg once daily for patients who are not able to tolerate 20 mg daily (i.e., for patients who experience any adverse events listed in Table 1).

Monitor patients carefully after dosage reduction and after stopping therapy with Leflunomida Jenson Pharmaceutical Services, since the active metabolite of Leflunomida Jenson Pharmaceutical Services, teriflunomide, is slowly eliminated from the plasma. After stopping Leflunomida Jenson Pharmaceutical Services treatment, an accelerated drug elimination procedure is recommended to reduce the plasma concentrations of the active metabolite, teriflunomide. Without use of an accelerated drug elimination procedure, it may take up to 2 years to reach undetectable plasma teriflunomide concentrations after stopping Leflunomida Jenson Pharmaceutical Services.

Evaluation and Testing Prior to Starting Leflunomida Jenson Pharmaceutical Services

Prior to starting Leflunomida Jenson Pharmaceutical Services treatment the following evaluations and tests are recommended:

More about Leflunomida Jenson Pharmaceutical Services (Leflunomida Jenson Pharmaceutical Services)

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Leflunomida Jenson Pharmaceutical Services interactions

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What other drugs will affect Leflunomida Jenson Pharmaceutical Services?

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Following oral administration, Leflunomida Jenson Pharmaceutical Services is metabolized to an active metabolite, teriflunomide, which is responsible for essentially all of Leflunomida Jenson Pharmaceutical Services's in vivo activity. Drug interaction studies have been conducted with both Leflunomida Jenson Pharmaceutical Services (Leflunomida Jenson Pharmaceutical Services) and with its active metabolite, teriflunomide, where the metabolite was directly administered to the test subjects.

Effect of Potent CYP and Transporter Inducers

Leflunomida Jenson Pharmaceutical Services is metabolized by CYP450 metabolizing enzymes. Concomitant use of Leflunomida Jenson Pharmaceutical Services and rifampin, a potent inducer of CYP and transporters, increased the plasma concentration of teriflunomide by 40%. However, when co-administered with the metabolite, teriflunomide, rifampin did not affect its pharmacokinetics. No dosage adjustment is recommended for Leflunomida Jenson Pharmaceutical Services when coadministered with rifampin. Because of the potential for Leflunomida Jenson Pharmaceutical Services concentrations to continue to increase with multiple dosing, caution should be used if patients are to be receiving both Leflunomida Jenson Pharmaceutical Services and rifampin.

Effect on CYP2C8 Substrates

Teriflunomide is an inhibitor of CYP2C8 in vivo. In patients taking Leflunomida Jenson Pharmaceutical Services, exposure of drugs metabolized by CYP2C8 (e.g., paclitaxel, pioglitazone, repaglinide, rosiglitazone) may be increased. Monitor these patients and adjust the dose of the concomitant drug(s) metabolized by CYP2C8 as required.

Effect on Warfarin

Coadministration of Leflunomida Jenson Pharmaceutical Services with warfarin requires close monitoring of the international normalized ratio (INR) because teriflunomide, the active metabolite of Leflunomida Jenson Pharmaceutical Services, may decrease peak INR by approximately 25%.

Effect on oral Contraceptives

Teriflunomide may increase the systemic exposures of ethinylestradiol and levonorgestrel. Consideration should be given to the type or dose of contraceptives used in combination with Leflunomida Jenson Pharmaceutical Services.

Effect on CYP1A2 Substrates

Teriflunomide, the active metabolite of Leflunomida Jenson Pharmaceutical Services, may be a weak inducer of CYP1A2 in vivo. In patients taking Leflunomida Jenson Pharmaceutical Services, exposure of drugs metabolized by CYP1A2 (e.g., alosetron, duloxetine, theophylline, tizanidine) may be reduced. Monitor these patients and adjust the dose of the concomitant drug(s) metabolized by CYP1A2 as required.

Effect on Organic Anion Transporter 3 (OAT3) Substrates

Teriflunomide inhibits the activity of OAT3 in vivo. In patients taking Leflunomida Jenson Pharmaceutical Services, exposure of drugs which are OAT3 substrates (e.g., cefaclor, cimetidine, ciprofloxacin, penicillin G, ketoprofen, furosemide, methotrexate, zidovudine) may be increased. Monitor these patients and adjust the dose of the concomitant drug(s) which are OAT3 substrates as required.

Effect on BCRP and Organic Anion Transporting Polypeptide B1 and B3 (OATP1B1/1B3) Substrates

Teriflunomide inhibits the activity of BCRP and OATP1B1/1B3 in vivo. For a patient taking Leflunomida Jenson Pharmaceutical Services, the dose of rosuvastatin should not exceed 10 mg once daily. For other substrates of BCRP (e.g., mitoxantrone) and drugs in the OATP family (e.g., methotrexate, rifampin), especially HMG-Co reductase inhibitors (e.g., atorvastatin, nateglinide, pravastatin, repaglinide, and simvastatin), consider reducing the dose of these drugs and monitor patients closely for signs and symptoms of increased exposures to the drugs while patients are taking Leflunomida Jenson Pharmaceutical Services.

Leflunomida Jenson Pharmaceutical Services side effects

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What are the possible side effects of Leflunomida Jenson Pharmaceutical Services?

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The following serious adverse reactions are described elsewhere in the labeling:

Clinical Trials Experience

Because clinical studies are conducted under widely varying conditions, adverse reaction rates observed in the clinical studies of a drug cannot be directly compared to rates in the clinical studies of another drug and may not reflect the rates observed in practice.

In clinical studies (Trials 1, 2, and 3), 1,865 patients were treated with Leflunomida Jenson Pharmaceutical Services administered as either monotherapy or in combination with methotrexate or sulfasalazine. Patients ranged in age from 19 to 85 years, with an overall median age of 58 years. The mean duration of RA was 6 years ranging from 0 to 45 years.

Elevation of Liver Enzymes

Treatment with Leflunomida Jenson Pharmaceutical Services was associated with elevations of liver enzymes, primarily ALT and AST, in a significant number of patients; these effects were generally reversible. Most transaminase elevations were mild ( ≤ 2-fold ULN) and usually resolved while continuing treatment. Marked elevations ( > 3-fold ULN) occurred infrequently and reversed with dose reduction or discontinuation of treatment. Table 1 shows liver enzyme elevations seen with monthly monitoring in clinical trials Trial 1 and Trial 2. It was notable that the absence of folate use in Trial 3 was associated with a considerably greater incidence of liver enzyme elevation on methotrexate.

Table 1: Liver Enzyme Elevations > 3-fold Upper Limits of Normal (ULN) in Patients with RA in Trials 1, 2, and 3**

Trial 1 Trial 2 Trial 3*
Leflunomida Jenson Pharmaceutical Services 20 mg/day

(n= 182)

PL

(n=118)

MTX 7.5 - 15 mg/wk

(n=182)

Leflunomida Jenson Pharmaceutical Services 20mg/day

(n=133)

PL

(n=92)

SSZ 2.0 g/day

(n=133)

Leflunomida Jenson Pharmaceutical Services 20 mg/day

(n=501)

MTX 7.5 - 15 mg/wk

(n=498)

ALT (SGPT) > 3-fold ULN (n %) 8 (4.4) 3 (2.5) 5 (2.7) 2 (1.5) 1 (1.1) 2 (1.5) 13 (2.6) 83 (16.7)
Reversed to ≤ 2-fold ULN: 8 3 5 2 1 2 12 82
Timing of Elevation
0-3 Months 6 1 1 2 1 2 7 27
4-6 Months 1 1 3 - - - 1 34
7-9 Months 1 1 1 - - - - 16
10-12 Months - - - - - - 5 6
MTX = methotrexate, PL = placebo, SSZ = sulfasalazine, ULN = Upper limit of normal

*Only 10% of patients in Trial 3 received folate. All patients in Trial 1 received folate.

In a 6 month study of 263 patients with persistent active rheumatoid arthritis despite methotrexate therapy, and with normal LFTs, Leflunomida Jenson Pharmaceutical Services was administered to a group of 130 patients starting at 10 mg per day and increased to 20 mg as needed. An increase in ALT greater than or equal to three times the ULN was observed in 3.8% of patients compared to 0.8% in 133 patients continued on methotrexate with placebo.

Most Common Adverse Reactions

The most common adverse reactions in Leflunomida Jenson Pharmaceutical Services-treated patients with RA include diarrhea, elevated liver enzymes (ALT and AST), alopecia and rash. Table 2 displays the most common adverse reactions in the controlled studies in patients with RA at one year ( ≥ 5% in any Leflunomida Jenson Pharmaceutical Services treatment group).

Table 2: Percentage Of Patients With Adverse Events ≥ 5% In Any Leflunomida Jenson Pharmaceutical Services Treated Group in all RA Studies in Patients with RA

Placebo-Controlled Trials Active-Controlled Trials All RA Studies
Trial 1 and 2 Trial 3 Hypertension as a preexisting condition was overrepresented in all Leflunomida Jenson Pharmaceutical Services treatment groups in phase III trials

Adverse events during a second year of treatment with Leflunomida Jenson Pharmaceutical Services in clinical trials were consistent with those observed during the first year of treatment and occurred at a similar or lower incidence.

Less Common Adverse Reactions

In addition, in controlled clinical trials, the following adverse events in the Leflunomida Jenson Pharmaceutical Services treatment group occurred at a higher incidence than in the placebo group. These adverse events were deemed possibly related to the study drug.

Blood and Lymphatic System: leukocytosis, thrombocytopenia;

Cardiovascular: chest pain, palpitation, thrombophlebitis of the leg, varicose vein;

Eye: blurred vision, eye disorder, papilledema, retinal disorder, retinal hemorrhage;

Gastrointestinal: alkaline phosphatase increased, anorexia, bilirubinemia, flatulence, gamma-GT increased, salivary gland enlarged, sore throat, vomiting, dry mouth;

General Disorders: malaise;

Immune System: anaphylactic reaction;

Infection: abscess, flu syndrome, vaginal moniliasis;

Nervous System: dizziness, headache, somnolence;

Respiratory System: dyspnea;

Post Marketing Experience

The following additional adverse reactions have been identified during postapproval use of Leflunomida Jenson Pharmaceutical Services. Because these reactions are reported voluntarily from a population of uncertain size, it is not always possible to reliably estimate their frequency or establish a causal relationship to drug exposure.

Blood and Lymphatic System: agranulocytosis, leukopenia, neutropenia, pancytopenia;

Infection: opportunistic infections, severe infections including sepsis;

Gastrointestinal: acute hepatic necrosis, hepatitis, jaundice/cholestasis, pancreatitis; severe liver injury such as hepatic failure

Immune System: angioedema;

Nervous system: peripheral neuropathy;

Respiratory: interstitial lung disease, including interstitial pneumonitis and pulmonary fibrosis, which may be fatal;

Skin and Appendages: erythema multiforme, Stevens-Johnson syndrome, toxic epidermal necrolysis, vasculitis including cutaneous necrotizing vasculitis, cutaneous lupus erythematosus, pustular psoriasis or worsening psoriasis.

Leflunomida Jenson Pharmaceutical Services contraindications

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Known hypersensitivity to Leflunomida Jenson Pharmaceutical Services or to any of the components of Leflunomida Jenson Pharmaceutical Services.

Use in pregnancy: Leflunomida Jenson Pharmaceutical Services can cause fetal harm when administered to pregnant women.

Women of Childbearing Potential: There are no adequate and well-controlled studies evaluating Leflunomida Jenson Pharmaceutical Services in pregnant women. However, based on animal studies, Leflunomida Jenson Pharmaceutical Services may increase the risk of fetal death or teratogenic effects when administered to a pregnant woman. Women of childbearing potential must not be started on Leflunomida Jenson Pharmaceutical Services until pregnancy is excluded and counseled on the potential for serious risk to the fetus. The patient must be advised that if there is any delay in onset of menses or any other reason to suspect pregnancy, notify the physician immediately for pregnancy testing, and if positive, the physician and the patient must discuss the risk to the pregnancy. It is possible that rapidly lowering the blood level of the active metabolite by instituting the drug elimination procedure as follows at the first delay of menses may decrease the risk to the fetus from Leflunomida Jenson Pharmaceutical Services. Upon discontinuing Leflunomida Jenson Pharmaceutical Services, it is recommended that all women of childbearing potential undergo the drug elimination procedure as described as follows. Women receiving Leflunomida Jenson Pharmaceutical Services treatment who wish to become pregnant must discontinue Leflunomida Jenson Pharmaceutical Services and undergo the drug elimination procedure which includes verification of M1 metabolite plasma levels <0.02 mg/mL (0.02 mcg/mL). Human plasma levels of the active metabolite (M1) <0.02 mg/L (0.02 mcg/mL) are expected to have minimal risk based on available animal data.

Drug Elimination Procedure: The following drug elimination procedure is recommended to achieve nondetectable plasma levels (<0.02 mg/L or 0.02 mcg/mL) after stoping treatment with Leflunomida Jenson Pharmaceutical Services: Administer cholestyramine 8 g 3 times daily for 11 days. The 11 days do not need to be consecutive unless there is a need to lower the plasma level rapidly.

Verify plasma levels <0.02 mg/L (0.02 mcg/mL) by 2 separate tests at least 14 days apart. If plasma levels are higher than 0.02 mg/L, additional cholestyramine treatment should be considered. Without the drug elimination procedure, it may take up to 2 years to reach plasma M1 metabolite levels <0.02 mg/L due to individual variation in drug clearance.



Active ingredient matches for Leflunomida Jenson Pharmaceutical Services:

Leflunomide in Portugal.


List of Leflunomida Jenson Pharmaceutical Services substitutes (brand and generic names)

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Unit description / dosage (Manufacturer)Price, USD
Tablet; Oral; Leflunomide 10 mg
Tablet; Oral; Leflunomide 20 mg
Arava 10 mg tablet$ 24.76
Arava 20 mg tablet$ 24.76
Leflunomide 10 mg tablet$ 16.75
Leflunomide 20 mg tablet$ 16.75
Tablets; Oral; Leflunomide 10 mg
Tablets; Oral; Leflunomide 20 mg
Leflunomide tablet, film coated 20 mg/1 (Prasco LLC (US))
Leflunomide tablet 20 mg (Sanis Health Inc (Canada))
Leflunomide tablet, film coated 10 mg/1 (Prasco LLC (US))
Leflunomide tablet 10 mg (Sanis Health Inc (Canada))
Leflunomide tablet 10 mg/1 (Trigen Laboratories, LLC (US))
Leflunomide tablet 20 mg/1 (Avera Mc Kennan Hospital (US))
Tablet; Oral; Leflunomide 10 mg
Tablet; Oral; Leflunomide 20 mg
Arava 10 mg tablet$ 24.76
Arava 20 mg tablet$ 24.76
Leflunomide 10 mg tablet$ 16.75
Leflunomide 20 mg tablet$ 16.75
Tablets; Oral; Leflunomide 10 mg
Tablets; Oral; Leflunomide 20 mg
Leflunomide tablet, film coated 20 mg/1 (Prasco LLC (US))
Leflunomide tablet 20 mg (Sanis Health Inc (Canada))
Leflunomide tablet, film coated 10 mg/1 (Prasco LLC (US))
Leflunomide tablet 10 mg (Sanis Health Inc (Canada))
Leflunomide tablet 10 mg/1 (Trigen Laboratories, LLC (US))
Leflunomide tablet 20 mg/1 (Avera Mc Kennan Hospital (US))
Tablet; Oral; Leflunomide 10 mg
Tablet; Oral; Leflunomide 20 mg
Arava 10 mg tablet$ 24.76
Arava 20 mg tablet$ 24.76
Leflunomide 10 mg tablet$ 16.75
Leflunomide 20 mg tablet$ 16.75
Tablets; Oral; Leflunomide 10 mg
Tablets; Oral; Leflunomide 20 mg
Leflunomide tablet, film coated 20 mg/1 (Prasco LLC (US))
Leflunomide tablet 20 mg (Sanis Health Inc (Canada))
Leflunomide tablet, film coated 10 mg/1 (Prasco LLC (US))
Leflunomide tablet 10 mg (Sanis Health Inc (Canada))
Leflunomide tablet 10 mg/1 (Trigen Laboratories, LLC (US))
Leflunomide tablet 20 mg/1 (Avera Mc Kennan Hospital (US))

References

  1. DailyMed. "LEFLUNOMIDE: DailyMed provides trustworthy information about marketed drugs in the United States. DailyMed is the official provider of FDA label information (package inserts).". https://dailymed.nlm.nih.gov/dailyme... (accessed September 17, 2018).
  2. PubChem. "leflunomide". https://pubchem.ncbi.nlm.nih.gov/com... (accessed September 17, 2018).
  3. DrugBank. "leflunomide". http://www.drugbank.ca/drugs/DB01097 (accessed September 17, 2018).

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