Huperio, 200 mg 28 pcs.

The action of the drug Juperio is mediated by a new mechanism, namely, the simultaneous inhibition of neprilysin activity (neutral endopeptidase, NEP) by the substance LBQ657 (active metabolite of sacubitril) and blockade of angiotensin II type 1 receptors (AT1) by valsartan, which is an antagonist of angiotensin II receptors (APA II).

Indications

Active ingredient

Composition

1 film-coated tablet, 200 mg (102.8 mg + 97.2 mg) contains:

Active ingredient:

Sacubitril and valsartan sodium salt hydrate complex -226.206 mg (in terms of 200 mg acid form anhydrous, which is equivalent to 97.2 sucubitril and 102.8 mg valsartan ;

Auxiliary substances:

Microcrystalline cellulose, 69.794 mg,

Hyprolose – 50,000 mg,

crospovidone – 36,000 mg,

magnesium stearate – 12,000 mg,

talc – 4,000 mg,

/p>

colloidal silicon dioxide – 2,000 mg;

coating:

white shell premix – 11.796 mg (hypromellose – 8.422 mg, titanium dioxide – 1.687 mg, macrogol 4000 – 0.843 mg, talc – 0.843 mg), red shell premix – 0.168 mg (hypromellose – 0.120 mg, Red iron oxide dye – 0.024 mg, macrogol 4000 -0.012 mg, talc 0.012 mg), black premix – 0.036 mg (hypromellose – 0.026 mg, iron oxide dye black 0.005 mg, macrogol 4000 – 0.003 mg, talc – 0.003 mg).

How to take, the dosage

The timing of taking Juperio is independent of the time of eating.

The target (maximum daily) dose of Huperio is 200 mg (102.8 mg + 97.2 mg) twice daily.

The drug can be used not earlier than 36 hours after ACE inhibitor withdrawal because angioedema may occur if used concomitantly.
As Valsartan ARA II is included in Huperio, it should not be used simultaneously with another drug that contains ARA II.

If patients have problems with tolerability of the drug (clinically pronounced BP decrease, hyperkalemia, impaired renal function), a temporary dose reduction or dose adjustment of concomitant medications should be considered.
Special categories of patients

Patients with renal dysfunction

In patients with renal dysfunction of mild (rCF 60-90 ml/min/1.73 m2) or moderate severity (rCF 30-60 ml/min/1.73 m2) the drug dose adjustment is not required. In patients with severe renal impairment (rSKF

Patients with hepatic impairment

In patients with mild hepatic impairment (class A according to the Child-Pugh classification) no dose adjustment of Huperio is required. In patients with moderate hepatic impairment (Child-Pugh class B), the recommended starting dose is 50 mg twice daily. Huperio is not recommended for use in patients with severe hepatic impairment (Child-Pugh class C).

The use in children and adolescents under 18 years of age

There are no data on the safety and effectiveness of Huperio in children and adolescents.

Usage in patients over 65 years of age

Dose adjustment is not required in patients over 65 years of age.

Interaction

Contraindicated drug interactions ACE inhibitors Imperio is contraindicated for use concomitantly with ACE inhibitors because suppression of nepralysin concomitantly with ACE inhibitor use may increase the risk of angioedema.

Uperio may be used no sooner than 36 hours after ACE inhibitor withdrawal. Use of an ACE inhibitor is possible no sooner than 36 hours after the last dose of Huperio.

Aliskiren

In patients with diabetes mellitus and in patients with impaired renal function (rCF)

Not recommended drug interactions

Angiotensin receptor antagonists

Because one of the active substances of the drug is an angiotensin II receptor antagonist, concomitant use with another drug containing ARA II is not recommended.

Drug interactions to be considered

HMG-CoA reductase inhibitors (statins)

The data from studies show that sacubitril inhibits the activity of OATP1B1 and OATP1BZ transporters. Huperio may increase systemic exposure to OATP1B1 and OATP1BZ substrates such as statins. In patients who received Juperio concomitantly with atorvastatin, maximum plasma concentrations (Cmax) of atorvastatin and its metabolites were increased up to 2 times, and AUC – up to 1.3 times. For this reason, Juperio should be used with caution concomitantly with statins.

Sildenafil

In patients with significant BP elevation receiving Huperio (before reaching equilibrium concentration), single use of sildenafil enhanced the antihypertensive effect compared to use of Huperio in monotherapy. For this reason, sildenafil or another type 5 phosphodiesterase inhibitor should be used with caution in patients receiving Huperio.

Presumed drug interactions to be considered

Potassium

Concomitant use of potassium-saving diuretics (e.g., triamterene and amiloride), mineralocorticoid antagonists (e.g., spironolactone and eplerenone), potassium products or potassium-containing table salt substitutes may cause increased potassium and serum creatinine concentrations. In patients receiving Juperio concomitantly with these drugs, it is recommended to monitor serum potassium levels regularly.

Non-steroidal anti-inflammatory drugs (NSAIDs), including selective cyclooxygenase-2 inhibitors (COX-2 inhibitors). The use of Huperio concomitantly with NSAIDs in patients over 65 years of age, in patients with hypovolemia (including patients receiving diuretics) and in patients with impaired renal function may increase the risk of impaired renal function. In patients receiving Juperio concomitantly with NSAIDs, it is recommended to monitor renal function when prescribing a similar treatment regimen and in case of its change.

Lithium preparations

The possibility of drug interaction between Huperio and lithium preparations has not been studied. Concomitant use of lithium with ACE inhibitors and ARA II has resulted in a reversible increase in serum lithium concentration and, therefore, in an increase in toxic effects. In patients receiving Juperio together with lithium preparations, it is recommended to carefully monitor the lithium content in blood serum. The risk of lithium toxicity may increase if additional diuretic medication is used.

The transporter proteins

The active metabolite of sacubitril (LBQ657) and valsartan are substrates of the transporter proteins 0ATP1B1, 0ATP1BZ and OATZ; valsartan is also a substrate of the transporter protein MRP2. Patients receiving Huperio concomitantly with OATP1B1, OATP1BZ, OATZ inhibitors (e.g., rifampicin and cyclosporine) or MRP2 (e.g., ritonavir) may have increased systemic exposure to LBQ657 or valsartan, respectively. Caution is required at the start and end of coadministration of Huperio and this group of drugs.

There are no significant drug interactions. No clinically significant interactions have been identified when Huperio is used in combination with furosemide, digoxin, warfarin, hydrochlorothiazide, amlodipine, metformin, omeprazole, carvedilol, IV nitroglycerin (IV) or a combination of levonorgestrel and ethinylestradiol.

Interactions with atenolol, indomethacin, glibenclamide (gliburide) or cimetidine are not expected when combined with Huperio.

Interactions with cytochrome P450 isoenzymes

The available studies demonstrate that the likelihood of drug interactions mediated by CYP450 cytochrome isoenzymes is low, because the active substance complex is only slightly metabolized with the participation of CYP450 isoenzymes. The active substance complex of Huperio is not an inhibitor or inducer of CYP450 isoenzymes.

Special Instructions

Significant decrease in BP

In patients treated with Huperio, there have been cases of clinically significant arterial hypotension. If a marked decrease in BP occurs, consideration should be given to adjusting the dose of diuretics, concomitant hypotensive agents, and the cause of the marked decrease in BP (e.g., hypovolemia). If, despite these measures, the pronounced BP decrease persists, the dose of Huperio should be reduced or the drug should be temporarily withdrawn. Definitive withdrawal of the drug is usually not required. The likelihood of significant BP decrease is generally higher in patients with hypovolemia, which may be caused by diuretic therapy, low-salt diet, diarrhea, or vomiting.

Before starting Hyperio, sodium should be corrected and/or the BOD should be replenished.

Kidney function impairment

Like any other drug acting on the RAAS, Huperio may cause impairment of renal function. In a comparative safety and efficacy study of 14/17 (compared with enalapril), clinically significant impairment of renal function was rare, and Huperio was withdrawn less frequently (0.65%) than enalapril (1.28%) for such impairment. In cases of clinically significant impairment of renal function, a reduction in the dose of Huperio should be considered. Caution should be exercised when using Huperio in patients with severe renal dysfunction.

Hyperkalemia

Like any other drug acting on the RAAS, Huperio may increase the risk of hyperkalemia. In a comparative safety and efficacy study (compared with enalapril), clinically significant hyperkalemia was rare; hyperkalemia was withdrawn due to hyperkalemia in 0.26% of patients and enalapril in 0.35% of patients. Drugs that may increase serum potassium levels (e.g., potassium-saving diuretics, potassium preparations) should be used with caution concomitantly with Huperio. In case of clinically significant hyperkalemia, measures such as reducing potassium intake with food or adjusting the dose of concomitant drugs should be considered. Regular monitoring of serum potassium is recommended, especially in patients with risk factors such as severe renal dysfunction, diabetes mellitus, hypoaldosteronism, or a diet high in potassium.

Anhyoneurotic edema

In cases of angioedema have been reported with the use of Huperio. If angioedema occurs, Imperio should be stopped immediately and the patient should be appropriately treated and monitored until all symptoms have resolved completely and permanently. Reapplication of Huperio should not be repeated. In cases of confirmed angioedema, where the swelling was limited to the face and lips, the condition usually resolved without intervention, although use of antihistamines did ameliorate the symptoms.

Contraindications

Side effects

Overdose

There are insufficient data on overdose with Huperio in humans. A single dose of 1200 mg and multiple doses of 900 mg in healthy volunteers were well tolerated.

The most likely symptom of overdose is a marked decrease in BP due to the antihypertensive effect of the active substances. Symptomatic treatment is recommended in this case.

In case of accidental overdose, vomiting should be induced (if the drug was taken recently) or gastric lavage should be performed. In case of pronounced BP decrease intravenous injection of 0.9% sodium chloride solution is necessary as therapy, the patient should be laid with his legs elevated for the time required for therapy, active measures on cardiovascular system support, including regular monitoring of heart and respiratory system activity, circulating blood volume (CBV) and amount of urine excreted should be taken.

The removal of active ingredients during hemodialysis is unlikely because much of it is bound to plasma proteins.

Pregnancy use