Lipirate 160 Uses

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What is Lipirate 160?

Lipirate 160 (Lipirate 160) helps reduce cholesterol and triglycerides (fatty acids) in the blood. High levels of these types of fat in the blood are associated with an increased risk of atherosclerosis (clogged arteries).

Lipirate 160 is used to treat high cholesterol and high triglyceride levels.

Lipirate 160 may also be used for purposes not listed in this medication guide.

Lipirate 160 indications

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Primary Hypercholesterolemia or Mixed Dyslipidemia

Lipirate 160 Capsules are indicated as adjunctive therapy to diet to reduce elevated low-density lipoprotein cholesterol (LDL-C), total cholesterol (total-c), Triglycerides (TG) and apolopoprotein B (Apo B), and to increase high-density lipoprotein cholesterol (HDL-C) in adult patients with primary hypercholesterolemia or mixed dyslipidemia.

Severe Hypertriglyceridemia

Lipirate 160 Capsules are also indicated as adjunctive therapy to diet for treatment of adult patients with severe hypertriglyceridemia. Improving glycemic control in diabetic patients showing fasting chylomicronemia will usually obviate the need for pharmacologic intervention.

Markedly elevated levels of serum triglycerides (e.g. > 2,000 mg/dL) may increase the risk of developing pancreatitis. The effect of Lipirate 160 therapy on reducing this risk has not been adequately studied.

Important Limitations of Use

Lipirate 160 at a dose equivalent to 150 mg was not shown to reduce coronary heart disease morbidity and mortality in 2 large, randomized controlled trials of patients with type 2 diabetes mellitus.

How should I use Lipirate 160?

Use Lipirate 160 capsules 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 Lipirate 160 capsules.

Uses of Lipirate 160 in details

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Use: Labeled Indications

Hypercholesterolemia or mixed dyslipidemia: Adjunctive therapy to diet for the reduction of low-density lipoprotein cholesterol (LDL-C), total cholesterol (total-C), triglycerides, and apolipoprotein B (apo B), and to increase high-density lipoprotein cholesterol (HDL-C) in adults with primary hypercholesterolemia or mixed dyslipidemia (Fredrickson types IIa and IIb). Use lipid-altering agents in addition to a diet restricted in saturated fat and cholesterol when response to diet and nonpharmacological interventions alone has been inadequate.

Note: While FDA-approved for hypercholesterolemia, Lipirate 160 is not a first- or second-line choice; other agents may be more suitable (ACC/AHA [Stone 2013]). In addition, use is not recommended to lower LDL-C or raise HDL-C in the absence of hypertriglyceridemia.

Hypertriglyceridemia: Adjunctive therapy to diet for treatment of adult patients with severe hypertriglyceridemia (Fredrickson types IV and V hyperlipidemia).

Off Label Uses

Primary biliary cholangitis

Data from a single-center, retrospective cohort study support the use of Lipirate 160 (in combination with ursodiol) in patients with primary biliary cholangitis (PBC) who have had an incomplete biochemical response to ursodiol monotherapy and showed significant improvement in alkaline phosphatase, a reduction in hepatic decompensation, and transplant-free survival improvement.

Lipirate 160 description

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Each film-coated tablet contains Fenofibrate BP 160 mg. It also contains the following excipients: Pregelatinized starch maize, povidone, sodium lauryl sulphate, microcrystalline cellulose, crospovidone, anhydrous colloidal silica, sodium stearyl fumarate, purified water and opadry AMB OY-B-28920.

Lipirate 160 is a lipid-regulating agent. The empirical formula is C20H21O4Cl and the molecular weight is 360.83. Lipirate 160 is 2-[4-(4-chlorobenzoyl) phenoxy]-2-methyl-propanoic acid, 1-methylethyl ester.

Lipirate 160 dosage

Lipirate 160 Dosage

Generic name: Lipirate 160 160mg

Dosage form: tablet

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

​The dose of Lipirate 160 is 160 mg once daily.

​Patients should be placed on an appropriate lipid-lowering diet before receiving Lipirate 160 and should continue this diet during treatment with Lipirate 160.

​Lipid levels should be monitored periodically. Therapy should be withdrawn in patients who do not have an adequate response after two months of treatment.

​Lipirate 160 tablets can be given without regard to meals. Patients should be advised to swallow Lipirate 160 tablets whole. Do not crush, break, dissolve, or chew tablets.

More about Lipirate 160 (Lipirate 160)

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Lipirate 160 interactions

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What other drugs will affect Lipirate 160?

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Coumarin Anticoagulants

Potentiation of coumarin-type anticoagulant effect has been observed with prolongation of the PT/INR.

Caution should be exercised when Lipirate 160 is given in conjunction with coumarin anticoagulants. Lipirate 160 may potentiate the anticoagulant effect of these agents resulting in prolongation of the PT/INR. To prevent bleeding complications, frequent monitoring of PT/INR and dose adjustment of the oral anticoagulant as recommended until the PT/INR has stabilized.

Immunosuppressants

Immunosuppressant agents such as cyclosporine and tacrolimus can impair renal function and because renal excretion is the primary elimination route of fibrate drugs including Lipirate 160 capsules, there is a risk that an interaction will lead to deterioration of renal function. When immunosuppressants and other potentially nephrotoxic agents are co-administered with Lipirate 160 capsules, the lowest effective dose of Lipirate 160 capsules should be employed and renal function should be monitored.

Bile-Acid Binding Resins

Since bile-acid binding resins may bind other drugs given concurrently, patients should take Lipirate 160 at least 1 hour before or 4 to 6 hours after a bile acid binding resin to avoid impeding its absorption.

Colchicine

Cases of myopathy, including rhabdomyolysis, have been reported with fenofibrates co-administered with colchicine, and caution should be exercised when prescribing Lipirate 160 with colchicine.

Lipirate 160 side effects

See also:
What are the possible side effects of Lipirate 160?

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.

Fenofibric acid is the active metabolite of Lipirate 160. Adverse events reported by 2% or more of patients treated with Lipirate 160 and greater than placebo during double-blind, placebocontrolled trials are listed in Table 1. Adverse events led to discontinuation of treatment in 5.0% of patients treated with Lipirate 160 and in 3.0% treated with placebo. Increases in liver tests were the most frequent events, causing discontinuation of Lipirate 160 treatment in 1.6% of patients in double-blind trials.

Table 1: Adverse Events Reported by 2% or More of Patients Treated with Lipirate 160 and Greater than Placebo During the Double-Blind, Placebo-Controlled Trials

BODY SYSTEM Adverse Event Lipirate 160*

(N = 439)

Placebo

(N = 365)

BODY AS A WHOLE
Abdominal Pain 4.6% 4.4%
Back Pain 3.4% 2.5%
Headache 3.2% 2.7%
DIGESTIVE
Nausea 2.3% 1.9%
Constipation 2.1% 1.4%
INVESTIGATIONS
Abnormal Liver Tests 7.5% 1.4%
Increased AST 3.4% 0.5%
Increased ALT 3.0% 1.6%
Increased Creatine Phosphokinase 3.0% 1.4%
RESPIRATORY
Respiratory Disorder 6.2% 5.5%
Rhinitis 2.3% 1.1%
* Dosage equivalent to 135 mg Lipirate 160

Clinical trials with Lipirate 160 did not include a placebo-control arm. However, the adverse event profile of Lipirate 160 was generally consistent with that of Lipirate 160. The following adverse events not listed above were reported in ≥ 3% of patients taking Lipirate 160 alone:

Gastrointestinal Disorders: Diarrhea, dyspepsia

General Disorders and Administration Site Conditions: Pain

Infections and Infestations: Nasopharyngitis, sinusitis, upper respiratory tract infection

Musculoskeletal and Connective Tissue Disorders: Arthralgia, myalgia, pain in extremity

Nervous System Disorders: Dizzinesss

Postmarketing Experience

The following adverse events have been identified during postapproval use of Lipirate 160: rhabdomyolysis, pancreatitis, renal failure, muscle spasms, acute renal failure, hepatitis, cirrhosis, anemia, asthenia, and severely depressed HDL-cholesterol levels.

Because these events 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.

Lipirate 160 contraindications

See also:
What is the most important information I should know about Lipirate 160?

Hypersensitivity to Lipirate 160 or fenofibric acid or to any of the excipients of Lipirate 160.

Severe renal impairment/insufficiency, including those receiving dialysis.

Active liver disease/dysfunction/insufficiency, including those with primary biliary cirrhosis and unexplained persistent liver function abnormalities eg, persistent elevations in serum transaminases. Pre-existing gallbladder disease.

Photoallergy or phototoxic reaction during treatment with fibrates or ketoprofen.

Chronic or acute pancreatitis with the exception of acute pancreatitis due to severe hypertriglyceridemia.

Lipirate 160 contains lecithin soya as an excipient and therefore, Lipirate 160 should not be taken with allergic to peanut or arachis oil or soya lecithin, or related products due to the risk of hypersensitivity reactions.

Use in lactation: Lipirate 160 should not be used in nursing mothers. Because of the potential for tumorigenicity seen in animal studies, a decision should be made whether to discontinue nursing or to discontinue Lipirate 160, taking into account the importance of Lipirate 160 to the mother. There are no data on the excretion of Lipirate 160 and/or its metabolites into breast milk.

Use in children: Safety and effectiveness in pediatric patients aged <18 years have not been established.



Active ingredient matches for Lipirate 160:

Fenofibrate in Vietnam.


Unit description / dosage (Manufacturer)Price, USD
Lipirate 160 160 mg x 5 Blister x 10 Tablet

List of Lipirate 160 substitutes (brand and generic names):

Lipirate 100 mg x 5 Blister x 10 Tablet
LIPIREG 160 MG TABLET 1 strip / 10 tablets each (Alembic Pharmaceuticals Ltd)$ 0.82
Lipireg 160mg Tablet (Alembic Pharmaceuticals Ltd)$ 0.08
Capsule; Oral; Fenofibrate 200 mg (Sanofi-aventis)
Capsule; Oral; Fenofibrate 67 mg (Sanofi-aventis)
Capsule; Oral; Fenofibrate 100 mg (Nobel)
Capsule; Oral; Fenofibrate 150 mg (Nobel)
Capsule; Oral; Fenofibrate 50 mg (Nobel)
30 capsule in 1 bottle, plastic (Nobel)
90 capsule in 1 bottle, plastic (Nobel)
Lipofen capsule 150 mg/1 (Nobel)
Lipofen capsule 50 mg/1 (Nobel)
Lipoprothyl 160 mg
Lipothin 200 200 mg x 3 x 10's
Capsule; Oral; Fenofibrate 100 mg (Aventis)
Capsule; Oral; Fenofibrate 250 mg
Lipway SR 250 mg x 30's (Cathay)$ 22.00
Lipway SR MR cap 250 mg 30's (Cathay Drug)$ 23.15
100 capsule in 1 bottle (Pharos)

References

  1. DailyMed. "FENOFIBRATE: 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. "fenofibrate". https://pubchem.ncbi.nlm.nih.gov/com... (accessed September 17, 2018).
  3. DrugBank. "fenofibrate". http://www.drugbank.ca/drugs/DB01039 (accessed September 17, 2018).

Reviews

The results of a survey conducted on ndrugs.com for Lipirate 160 are given in detail below. The results of the survey conducted are based on the impressions and views of the website users and consumers taking Lipirate 160. We implore you to kindly base your medical condition or therapeutic choices on the result or test conducted by a physician or licensed medical practitioners.

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Information checked by Dr. Sachin Kumar, MD Pharmacology

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