EDNYT 5mg Gedeon medicine for hypertension, heart failure (3 blisters x 10 tablets)

Dosage form Box of 3 blisters x 10 tablets
Specifications Enalapril

Ingredient

Composition informationContent
Enalapril5mg

Uses

indications

EDNYT 5mg drug is indicated in the following cases:

  • Hypertension.
  • heart failure.

    Preventive patients with symptoms of coronary anemia and heart failure in patients with left ventricular failure.

    Pharmacokological

    enalapril Maleat is an angiotensin moving inhibitor. Angiotensin (ACE) conversion enamel is a peptidyl dipeptidase peptidyl catalyst reaction to convert angiotensin I into angiotensin II vasoconstriction. After absorption, Enalapril is hydrolyzed into enalaprilate, inhibiting ACE. The inhibition of ACE reduces angiotensin II in plasma should increase lyin activity in plasma (because of the negative response of the release of renin), and reducing Aldosteron secretion.

    ACE is similar to Kininase II. Therefore, Enalapril Maleat can also inhibit Bradykinin decomposition, a strong vasoconstriction peptide. However, its role in Enalapril's treatment effect is still unknown.

    While Enalapril's blood pressure lowering mechanism is said to mainly inhibit the Renin Angiotensin-Aldosteron system, the system plays the main role in regulating blood pressure, in fact Enalapril has anti-hypertension effect even in low-blood pressure patients with low renin.

    Using Enalapril for patients with hypertension reduces blood pressure and stands without increasing the heart rate significantly.

    Symptoms of posture hypotension are less likely. In some patients, it takes a few weeks to treat to achieve optimal blood pressure decrease. Stop Enalapril Maleat suddenly does not cause soaring blood pressure.

    ACE activity inhibitors occur from 2-4 hours after taking the single-dose of Enalapril. Anti-hypertension effects appear after 1 hour, blood pressure reaches a maximum reduction after drinking 4-6 hours. The time period is related to the dose. However, in the recommended dose, anti -hypertension and hemodynamic effects are maintained for at least 24 hours.

    In hemodynamic studies with enalapril in patients with idiopathic hypertension, reducing blood pressure is often accompanied by a decrease in peripheral artery resistance and an increase in cardiac intake without changing heart rate or small change. After taking Enalapril, blood circulation through the kidneys increases; The speed of glomerular filtration is constant. There is no evidence of sodium and water retention. However, in patients with glomerular filtration rate before low treatment, this speed will usually increase.

    In short -term clinical research in patients with diabetes and no diabetes with kidney disease, after using Enalapril, the amount of albuminuria and IgG excretion and the total amount of proteinuria decreased.

    When used with the thiazid diuretic, the hypotension effect of Ednyt is the bronze. Ednyt can reduce or prevent hypokalemia caused by drugs. In patients with heart failure treated with digitalis and diuretics, oral or injection enalapril often reduces peripheral and blood pressure resistance. Supply of heart increases, while heart rate decreases (normal heart rate increases in patients with heart failure). Pulmonary capillary pressure also decreases. The drug has the effect of improving the severity of heart failure when measured by NYHA standard (New York Heart Association) and exertion test; These effects are maintained during long -term treatment.

    In patients with mild to medium -sized heart failure, Enalapril slowed down the progression of dilatation and/or heart hypertrophy and heart failure (shown by the decrease in the end of the diastolic and left ventricular systolic, and improves blood pressure fraction).

    still limiting experience in children over 6 years old with hypertension. In a clinical study, 110 patients with hypertension were children from 6 to 16 years old with a weight> 20kg and the speed of glomerular filtration> 30 ml/min/1.73 m2, patients 50 kg dose 1.25; 5 or 40 mg daily.

    Use enalapril once a day reduces blood pressure in a dose dependence. The anti -hypertension effect depends on the dose of Enalapril is considered in subgroups (age, according to the classification of tanner, gender, race). However, with the lowest dose of the study, the dose of 0.625mg and the dose of 1.25 mg corresponds to the average dose of 0.02 mg/kg once a day, ineffective anti -hypertension. The maximum dose of research is 0.58 mg/kg (to 40 mg) once a day.

    Data on unwanted effects for children's patients is not different from adult patients.

    pharmacokinetic

    absorption

    Enalapril Maleat is quickly absorbed, the peak concentration in the serum is reached within 1 hour after drinking. Based on the urinary analysis, Enalapril's absorption level after taking Enalapril Maleat is about 60%. The absorption of Ednyt is not affected by food in the digestive tract.

    After absorption, Enalapril is hydrolyzed quickly and strongly into Enalaprilate, a strong enzyme inhibitor. Enalaprilat's peak in plasma concentration reached 4 hours after taking Enalapril in the form of tablets.

    Effective selling time for enalaprilat accumulation after many times drinking enalapril is I1 hours. In people with normal kidney function, the stable concentration of enalaprilat in serum is achieved after 4 days of treatment.

    Distribution

    Within the treatment concentration, Enalaprilate is attached to serum protein not exceeding 60%. Enalapril passed the placenta fence.

    Metabolism

    Except for transformation into Enalaprilat, there is no evidence that there is any other significant metabolism of Enalapril.

    Elimination

    Enalaprilat is excreted mainly through the kidneys. The main component in urine is Enalaprilate, accounting for about 40% of the dose, and Enalapril has not metabolized (about 20%). Effective sales time of Enalaprilat after many times taking Enalapril Maleat is 11 hours. After reaching a plasma concentration for at least 24 hours, the sale time in plasma varies from 5.6-14.8 hours.

    Characteristics of some patient groups

    kidney failure

    Enalapril and Enalaprilate exposure increases above patients with renal function. When used by 5 mg once a day, patients with mild to medium to medium (creatinine clearance is 40-60 ml/min) with AUC value in the stable state of enalaprilat approximately 2 times higher than normal kidney function patients.

    In patients with severe renal impairment (Creatinine clearance

    Children and teenagers

    Multi -dose pharmacokinetics research is conducted on 40 children with hypertension including men and women from 2 months old to

    Data shows AUC value (when the data is measured according to the dose ratio/weight of the body) increases with age, but no AUC increases when the data is measured in the ratio of body tank area. In a stable state, the effective sale time for the accumulation of Enalaprilate is 14 hours.

    breastfeeding women

    After taking a single dose of 20 mg in 5 women after birth, the average peak concentration in Enalapril's milk is 1.7 μg/l (ranging from 0.54 to 5.9 μg/l) at 4 to 6 hours after drinking. The average peak concentration of Enalaprilate is 1.7 μg/l (ranging from 1.2 to 2.2 μg/l); The peak concentration is achieved at different times in the 24 -hour period. Based on the concentration of the peak in milk, the maximum absorption amount is estimated in the baby only eating breast milk is about 0.16% of the mother's dosage adjusted according to weight.

    A woman taking the oral dose of Enalapril 10mg/day for 11 months has an Enalapril peak concentration in milk is 2 mcg/l after 4 hours of drug use and the peak concentration of Enalaprilate is 0.75 mcg/l after 9 hours of medication. The total content of Enalapril and Enalaprilat measured in milk for 24 hours, 141.44 mcg/l and 0.63 mcg/l respectively. Enalaprilate cannot be detected in milk (

    No enalaprilate concentration in milk (

    Before taking EDNYT 5mg Gedeon medicine for hypertension, heart failure (3 blisters x 10 tablets)

    How to use

    because the food does not affect the absorption of Ednyt, can take the drug before, during or after meals.

    Dosage

    Maximum daily dose is 40 mg.

    Time to drink Enalapril Maleat does not depend on meals, but should drink with a sufficient amount of water. The daily dose is usually taken once in the morning but can also be divided into two mornings and evening.

    Note:

    After taking the first dose, there may be hypotension in high -risk patients (patients with salt loss and/or water, for example after fertilizer, vomiting, diarrhea , diuretic treatment, patients with heart failure, hypertension with severe kidney or hypertension).

    In patients with severe hypertension or severe heart failure, the dose must be started and adjust the dose in the hospital.

    Dosage is recommended as follows:

    Dosage should be determined depending on the patient form and the response of blood pressure.

    Hypertension

    The starting dose is from 5mg to a maximum of 20mg, depending on the level of high blood pressure and the patient's condition. Use Ednyt 1 time a day.

    In the case of mild hypertension, the recommended starting dose is 5-10mg/day. Patients with renin-ankiotensin-aldosteron systems (for example: kidney hypertension, salt and/or water, heart loss, serious hypertension) may have strong hypotension after the first dose. The starting dose should start 5 mg or lower for these patients and need a doctor's supervision when the patient starts taking the drug.

    Pre -doses of dosage dosage can lead to a decline in circulatory volume and the risk of hypotension when starting to treat Enalapril. The starting dose should start 5 mg or lower in these patients. If possible, diuretics should be stopped for 2-3 days before starting treatment with Ednyt. Should monitor kidney function and serum potassium.

    Normal maintenance dose is 20mg once a day. Willow maintain up to 40 mg once a day.

    heart failure

    In the treatment of symptomatic heart failure, Enalapril is used as a supportive therapy for diuretics and when appropriate, with digitalis or beta blockers. The starting dose in patients with symptoms or asymptomatic left ventricular dysfunction is 2.5 mg and should be closely monitored to determine the initial impact on the blood pressure.

    In case the hypotension has no symptoms or has been effectively controlled after the starting dose of Enalapril in patients with heart failure, if the patient is well tolerated, the dose should be increased to the usual maintenance dose (20mg), the only dose or divided into 2 doses. The adjustment of the dose should be done for a period of 2 to 4 weeks. The maximum dose is 40 mg/day is divided into 2 times.

    Adjustment of the recommended dose in patients with heart failure/disorder of left ventricular dysfunction.

    week

    Dose (mg/day)

    week 1

    Day 1 to 3: 2.5 mg/day *, use only 1 time.

    4 to 7: 5 mg/day, divided into 2 times.

    Week 2

    10 mg/day, use 1 time or divided into 2 times.

    Week 3 and Week 4

    20 mg/day, use 1 time or divided into 2 times.

    For patients taking diuretics, the dose should be reduced if possible before starting treatment with Ednyt. Patients with hypotension after the first dose use Ednyt does not mean hypotension will continue to recur when long -term treatment with Ednyt and not necessarily stop the drug. Should monitor serum and kidney function.

    Dosage in patients with renal function

    Overall, the distance should be extended between enalapril and/or dose reductions.

    Creatinine clearance (CrCl)

    (ml/min)

    Initial dose (mg/day)

    5 - 10 mg

    2.5 mg

    2.5 mg/day of hemorrhage *

    Dosage in the days of non -hematurosis patients should be adjusted based on blood pressure response.

    Elderly: Dosage should be suitable for the kidney function of elderly patients.

    Children

    There is still limited clinical trials on the use of Ednyt in children with hypertension. For patients who can swallow the pills, the dose should be adjusted according to the individual based on the patient and responding on blood pressure. The starting dose is 2.5 mg for patients from 20 to less than 50kg and 5 mg for patients> = 50 kg. Take medication once a day. The dosage should be adjusted according to the needs of the patient with a maximum dose of 20 mg daily for patients from 20 to less than 50kg and 40 mg for patients> = 50 kg.

    It is not recommended to use Ednyt for babies and in children with the ratio of glomerular filtration

    Note: The above dose is for reference only. Specific dosage depends on the condition and level of progression of the disease. For a suitable dose, you need to consult a doctor or medical specialist.

    What to do when using overdose? The outstanding feature of the overdose report is severe hypotension, and with the Renin-Anotensin system that is blocked and dizzy, begins to occur about 6 hours after the drug.

    Symptoms that come with an overdose of enzyme inhibitors may include circulatory shock, electrolyte disorders, kidney failure, lung ventilation, tachycardia , chest drumming, slow heart rate , dizziness, anxiety and cough. After the dose of 300 mg and 440 mg Enalapril, the serum enalaprilate concentration is 100 and 200 times higher than the usual treatment.

    Treatment recommends overdose is intravenously physiological saline solution. If hypotension, patients should be placed in the site of shock treatment. If possible, treated with Angiotensin II or intravenous catecholamine.

    If the patient has just taken medicine, may be used to remove Enalapril Maleat (for example, causing vomiting, washing the intestine, using adsorbent, and sodium sulphat). Enalaprilate can be removed from circulation with hemolysis. Rhythmic therapy is indicated for anti -therapeutic heart rate. Need to continuously monitor the signs of life, serum electrolytes and creatinine levels.

    In an emergency, call the 115 emergency center immediately or go to the nearest local health station.

    What to do when forgetting a dose? However, if the time to relax with the next dose is too short, skip the dose and continue the calendar of the drug. Do not use double dose to compensate for missed dose.

    Side Effects

    When using the drug, you may experience unwanted effects (ADR).

    The following unwanted effects, usually mild and transient, have been recorded related to Enalapril Maleat or other enzyme inhibitors:

    The desired effect is listed in the following table according to the organ system and the frequency of meetings.

    Agency system

    !

    Uncommon (can be encountered at 1/100)

    Rare (can be encountered at 1/1000)

    Very rare (can be encountered at a rate of up to 1/10000) and unknown (not estimated from existing data)

    Anemia (including hemolytic anemia and aquatic anemia)

    Neutral leukopenia, hemoglobin reduction, hematocrit reduction, thrombocytopenia, grain leukemia, marrow failure, hypoglycemia, lymphatic disease, autoimmune disease

    Endocrine disorders

    Anti -compliant anti -hormone excretion syndrome (SIADH)

    Lower blood glucose

    Mental disorders

    depression

    Headache

    confused, sleeping, insomnia, agitation, abnormalities, dizziness

    abnormal dreams, sleep disorders

    ...

    tinnitus

    heart disorders

    Angina, chest pain, arrhythmia, tachycardia

    Brushing the chest, myocardial infarction (the ability to lower secondary blood pressure (3 high -risk patients)

    dizziness

    Fainting, hypotension (including hypotension)

    Blushing, hypotension with vertical posture, stroke * (The ability to lower secondary hypotension in high risk patients)

    Raynaud syndrome

    ho

    Difficulty breathing

    runny nose, sore throat, hoarseness, bronchospasm/asthma

    Infection with lungs, rhinitis, allergic alveoli/leukemia pneumonia

    nausea

    diarrhea, abdominal pain, taste change

    Bowel obstruction, inflammation, vomiting, indigestion, constipation, anorexia, stomach irritation, dry mouth, stomach ulcers

    Gastritis/ulcer, tongue

    gastrointestinal angioedema

    Hepatitis, VCNI liver (bile or liver cell form), hepatitis including necrosis, cholestasis (including jaundice)

    Red, hypersensitivity/angiography (there are reports on the angioed angio, limb, lips, tongue, bar, and/or larynx)

    Sweating, itching, urticaria, hair loss

    diverse roses, Stevens-Johnson syndrome, flaky dermatitis, poisoned epidermal necrosis, pemphigul, red skin **

    Cramping

    Renal dysfunction, kidney failure, proteinuria

    Big breasts in men

    weakness

    tired

    annoying, fever

    Examination

    Hypotension, increased serum creatinine

    Hypermath of blood, hypoglycemia

    liver enzyme, serum bilirubin increased

    ** Symptomic complexes may include a few or all of the following symptoms: fever, baritis, vasculitis, myocarditis/myocarditis, joint pain/arthritis, positive antibodies, increased rate of red blood cell settings, eosinophilia, eosinophilia, leukopenia. Can encounter redness, hypersensitivity to light or other skin manifestations.

    Notify the doctor with unwanted effects when using the drug.

    Warnings

    Before using the drug you need to read the instructions carefully and refer to the information below.

    Contraindicated

    Contraindications in the following cases:

  • Hypersensitivity to the active ingredient or any Angiotensin transferring inhibitor or any ingredients of the drug.
  • There is a history of vascular nerve edema due to the previous angiotensin enzyme inhibitors, spontaneous or genetic nerve edema.

    pregnancy.

  • Breastfeeding period.
  • Precautions when using

    Hypotension with symptoms

    Rarely hypotension symptoms in patients with hypertension without complications. In patients with enalapril hypertension, hypotension tends to occur if the patient has a decrease in the volume of circulatory, for example, due to diuretics, a diet that limits salt, feces, diarrhea or vomiting. In patients with heart failure, whether or not with renal failure, hypotension with symptoms has also been recorded.

    This is more likely to occur in patients with severe heart failure, reflecting the high doses of dosage, reducing blood sodium or kidney damage.

    In these patients, it is recommended to start treatment under medical monitoring and closely monitor patients when adjusting the dose of Enalapril and/or diuretics.

    Similar measures are also applied in patients with ischemic heart disease or cerebrovascular disease, which in these patients with excessive hypotension can lead to myocardial infarction or stroke.

    If the pressure occurs, the patient should be placed in a lying position and intravenously physiological saline solution if necessary. If the patient has a transient hemorrhagic response, there is no need to stop the drug and may continue to take the drug regularly after the blood pressure has increased by infusion.

    Some patients with heart failure with normal or low blood pressure may have an additional body blood pressure when using Ednyt. This impact is predicted and often is not the reason for stopping treatment. If symptomic hypotension occurs, it may be necessary to reduce the dose and/ or stop diuretics and/ or ednyt.

    Aortic stenosis or mitral stenosis /disease myocardial hypertrophy

    as well as vasodilators, angiotensin enzyme inhibitors must be used carefully in patients with left ventricular valve disease or left ventricular obstruction, and not in case of cardiac shock and significant hemodynamic obstruction.

    Renal function impairment

    In case of impaired renal function (Creatinine clearance

    Renal failure has been reported in Enalapril therapy and is mainly seen in patients with severe heart failure or suffering from kidney disease, including renal artery stenosis. If being recognized early and appropriate treatment, kidney failure in treatment with Enalapril is usually recovered.

    Some patients with hypertension with kidney disease without obvious manifestation may have hyperurin and blood creatinine when using enalapril simultaneously and diuretics. Enalapril and/or diuretics may be reduced. This case may have to consider the possibility of patients with renal artery stenosis.

    Renal hypertension

    The risk of hypotension and renal failure increases when the patient has renal artery stenosis on both sides of the kidneys or the kidney stenosis in humans has only one kidney when treated by angiotensin enzyme inhibitors. Loss of kidney function can occur with only small changes in serum creatinine, need to monitor medical closely when starting therapy with low dose, careful dose and monitor kidney function.

    kidney transplant

    There is no experience related to using Ednyt in patients who have just had kidney transplant. Therefore, it is not recommended to use Ednyt in this case.

    Hepatic failure

    Rarely reports related to angiotensin transferring enzymes with jaundice starting with bile jaundice or hepatitis and progressing into violent necrosis that sometimes leads to death. The mechanism of this syndrome is not well understood. Patients taking angiotensin transferring enzymes inhibitors with jaundice or increasing liver enzyme must be clearly stopped and monitored by appropriate measures.

    Neutral leukemia/grain leukemia

    Neutral leukemia/grain leukemia, reduced platelet and anemia has been recorded in patients with ACE inhibitors. Rarely occurs neutrophils in patients with normal renal function and no complications.

    Should use enalapril very carefully in patients with blood vessel disease, which is treating immunosuppressive, is using allopurinol or processaamid or has a combination of these complications, especially in patients with previous renal function.

    Some patients have serious infections without responding to positive antibiotic therapy. If using enalapril in these patients should periodically monitor the number of white blood cells and require the patient to report immediately if there is any sign of infection.

    sensitivity/angioedema

    Facility on the face, limbs, lips, tongue, subjects and/or throat have been encountered in patients treated with angiotensin transferring enamel inhibitors, including Ednyt. These side effects can be encountered at any time during treatment.

    In these cases, Ednyt must be stopped immediately and monitor patients with appropriate measures to ensure that the patient has recovered from all the symptoms before discharged from the hospital. Even in cases when tongue swelling has been overcome without shortness of breath, still have to continue monitoring patients because treatment with antihistamine and corticosteroids may not be effective.

    There have been reports on veins related to laryngeal edema or tongue edema but very rare. Patients with tongue edema, bar or larynx can be obstructed, especially those with a history of airway surgery. When there is a reaction on the tongue, the bar or larynx causes airway obstruction, it is necessary to quickly apply the appropriate treatment therapy that may include epinephrin solution (1: 1000) (0.3 ml to 0.5 ml) and/or use measures to ensure ventilation.

    Black racial patients use Angiotensin transferred inhibitors with higher angio rates than patients of other skin -colored races.

    Patients with a history of angioemia are not related to angiotensin transferred enzyme inhibitors may increase the risk of angioed with enamel inhibitors.

    Anaphylactic reaction in sensitive removal therapy with winged insects:

    Very rare anaphylactic reaction threatens life in patients using angiotensin transferring enzyme inhibitors during sensitivity with serum winged insect venom. These reactions can be prevented by temporarily stopping the enzyme inhibitors before each sensitivity.

    Anaphylactic reaction in LDL dialysis therapy

    Rare anaphylactic reactions that threaten life in patients using angiotensin enzyme inhibitors in lipoprotein dialysis therapy with low molecular weight (LDL) with dextran sulfate. These reactions can be prevented by temporarily stopping the enzyme inhibitors before each dialysis.

    Patients with hemolysis

    There has been anaphylactic reaction report in patients with high pine membranes (for example, an69) and is treated simultaneously with enzyme inhibitors. For these patients, it is necessary to consider using different types of fertilizer membranes or taking another group of hypertension.

    Lower blood glucose

    On patients with diabetes treated with oral diabetes or insulin, when starting treatment with angiotensin transferring enzyme inhibitors must be advised to closely monitor blood glucose, especially in the first month of medication.

    ho

    There have been a cough show when using angiotensin transferring enzyme inhibitors. This cough is described as a dry and persistent cough but after stopping the drug. Coughing due to transferred enzyme inhibitors should be considered as part of the diagnosis of cough.

    surgery/anesthesia

    Enalapril prevents the establishment of the secondary Angiotensin II from the release of re -release in patients with surgery or anesthetics with anti -blood pressure. If the patient has hypotension, this mechanism should be considered and should adjust this hypotension by compensation.

    Hemorrhage hyperka

    Hemorrhage hyperpathy may occur during treatment of angiotensin transferring enzyme inhibitors including enalapril. Yếu tố nguy cơ bị tăng kali máu là: Bệnh nhân suy thận, suy giảm chức năng thận, tuổi tác (>70 tuổi), đái tháo đường, các triệu chứng tái phát, bệnh nhân mất nước, mất bù tim cấp, nhiễm toan chuyển hóa và dùng đồng thời các thuốc lợi tiểu giữ kali (ví dụ: Spironolacton, eplerenon, triamteren hoặc amilorid), thuốc bù kali hoặc các chất thay thế muối chứa kali hoặc trên các bệnh nhân dùng thuốc có thể làm tăng Blood potassium (for example: heparin).

    The use of potassium, diuretic drugs that keep potassium, salt -containing potassium -containing salt in patients with impaired renal function can lead to significant increase in potassium potassium. Hyperboly hyperkalemia can cause serious arrhythmia, sometimes leading to death. If using Enalapril simultaneously and one of the above factors, it is necessary to be cautious and regularly monitor blood potassium.

    lithium

    generally do not recommend combining lithium and enalapril.

    lactose

    Each EDNYT 10mg tablet contains 100 mg of lactose. Therefore, patients do not tolerate congenital galactose, deficiency of lapp lactase or absorbent glucose-galactose should not use this drug.

    Children

    still limit the experience of safety and effectiveness in children over 6 years old with hypertension, no experience with other indications. The pharmacokinetic material for children over 2 months of age is limited. In addition to ordering hypertension, it is not recommended to use EDNYT for children for other indications.

    It is not recommended to use Ednyt for babies and children with glomerular filtration speed below 30 ml/min/1.73 m2 because there is no data.

    Race difference

    Like the enzyme inhibitors Angiotensin, Enalapril is clearly less effective to lower blood pressure on black people rather than other skin races. This may be because the proportion of black people with hypertension has a higher renin condition than other skin races.

    The ability to drive and operate machinery

    There are no studies on the effect of this drug on the ability to drive. When driving or operating the machine, remember that sometimes the drug causes drowsiness and fatigue.

    Pregnancy

    The use of Ednyt is contraindicated during pregnancy and lactation.

    The evidence of epidemiology has not been identified after the risk of teratogenicity after the mother uses Angiotensin transferring enzyme inhibitors in the first quarter of pregnancy, but the small rate increases the risk of not being excluded. Except for the continued use of angiotensin transferring enzyme inhibitors, patients planning to get pregnant, so they should switch to other hypertension drugs that have been shown to be safe during pregnancy. When diagnosed with pregnancy, it is advisable to stop treating with angiotensin transferring enzyme inhibitors immediately and if appropriate, then start another alternative therapy.

    Using angiotensin transferring enzyme inhibitors in the second quarter and the third quarter of pregnancy causes fetal toxicity (reducing kidney function, less amniotic fluid, slow chemistry of the skull) and infant poisoning (kidney failure, hypotension, hyperkalemia). If you use Angiotensin transferring enzyme inhibitors from the second quarter of pregnancy onwards, need for kidney and skull ultrasound.

    When the mother uses the Angiotensin transferring inhibitor, it is necessary to closely monitor the condition of hypotension on the child.

    Breastfeeding period

    limited dynamic pharmacokinetics data shows that low concentration of drugs in breast milk. Although these concentrations may not be clinically correlated, contraindicated to use Ednyt for breastfeeding women in case of premature birth or in the first few weeks after birth because there may be risk on the kidneys and cardiovascular disease and because there is no clinical experience. The decision to stop breastfeeding or stopping EDNYT should consider the benefits of breastfeeding and the benefits of the mother's treatment.

    Drug interaction

    Diuretics keep potassium or potassium compensation drug

    Angiotensin transferring enzyme inhibitors reduce potassium loss due to diuretics. Potassium diuretics such as spironolacton , triamteren or amilorid, potassium compensation drugs or salt -containing salt substitutes can significantly increase blood potassium. If indicated in combination with Spironolacton, the medication should be used carefully and regularly monitor the blood potassium.

    diuretics (thiazid or diuretics):

    High -dose dosage treatment can cause fluid loss and the risk of hypotension at the beginning of Bing Enalapril treatment. Hypotension effects can be reduced when diuretics stop, increase fluid, use salt or use enalapril therapy at low doses.

    Other anti -hypertension drugs

    Concentrated use of these drugs can increase the hypotension effect of Enalapril Maleat, especially with diuretics. Simultaneous use with nitroglycerin and other nitrates, or vasodilators can reduce blood pressure.

    Non -steroid anti -inflammatory drugs (NSAIDs): Non -steroid anti -inflammatory drugs can reduce the hypotension of the enzyme inhibitors in Angiotensin transfer. Concomitance nonsteroidal anti-inflammatory drugs (including COX-2 inhibitors) and angiotensin inhibitors that increase blood potassium and may cause kidney function. These effects are usually recovered.

    Acute renal failure may occur but rarely special for patients with kidney damage (for example, elderly people, patients with fluid loss including people who are being treated with diuretics). Patients need to be fully rehydrated and monitored the kidney function after starting combined treatment and periodic monitoring.

    lithium

    Hypermathy and recovery lithium lithium has been reported when used simultaneously lithium and enzyme inhibitors Angiotensin. Simultaneous use of thiazid diuretics may increase lithium concentration and increase the risk of lithium poisoning with angiotensin transfer enzyme inhibitors. It is not recommended to use the combination of enalapril and lithium but if the combination is necessary, closely monitor blood lithium

    alcohol

    Alcohol can increase the hypotension effect of angiotensin transferring enzyme inhibitors.

    Three -round antidepressants/anti -psychotic/anesthetic/addictive drugs.

    Blood pressure drops sharply (so it is necessary to notify the anesthetic doctor for treatment with Enalapril Maleat). Hypotension can be encountered when used simultaneously with addictive drugs/antidepressants.

    Parentive drugs

    Paralges can reduce the anti -hypertension effect of angiotensin transferring enzyme inhibitors.

    Ocean anti -diabetic drugs (e.g. Sulphonyl URE/ BiguanID), insulin.

    Epidemiological research shows that the use of angiotensin transferring enzymes and anti -diabetic drugs (insulin, oral blood glucose orally) may increase blood glucose reducing the risk of hypoglycemia. This phenomenon can occur in the first weeks combining treatment and in patients with renal function.

    Gold

    Nitritoid reactions (symptoms including facial furniture, nausea, vomiting and hypotension) have been reported but rarely in patients with injection yellow treatment (sodium urothomalate) and angiotensin transferring enzyme inhibitors including enalapril.

    Acetvlsalicylic acid , Blood soluble drugs and beta blockers

    Enalapril is safe when used simultaneously with acetysalicylic acid (at the dose of heart treatment), medications that soluble thrombosis and beta blockers.

    antacids

    can reduce the bioavailability of the enzyme inhibitors.

    Storage

    Leave a cool place, avoid light, temperature below 30⁰C.

    To be out of reach of children.

    Other drugs

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