Savi Valsartan 80 medicine for hypertension, myocardial infarction (3 blisters x 10 tablets)
Dosage form Box of 3 blisters x 10 tablets
Specifications Valsartan
Ingredient
| Composition information | Content |
| Valsartan | 80mg |
Uses
Indications
Savi Valsartan 80 drugs are indicated in the following cases:
Pharmacy
High blood pressure
Hormones are active of the renin-ankiotensin-aldosteron system (RAA) is angiotensin II; Formed from angiotensin I. Angiotensin II associated with some specific receptors on the cell membrane in the tissues. Angiotensin II has many physiological effects including direct and indirect participation in regulating blood pressure. As a substance capable of causing vasoconstriction, Angiotensin II causes a direct vascular pressure response. In addition, it has the effect of increasing salt retention and stimulating aldosteron secretion. Valsartan uses oral activity with specific antagonism with Angiotensin II receptor (ang.ii).
Select drugs on AT1 receptor -type (angiotensin II Receptor Type 1); This receptor controls the activity of ang.II. Ang.II concentration in serum when the AT1 receptor is inhibited with Valsartan, resulting in AT2 receptor activation; This receptor has a balanced effect with AT1 receptor.
Valsartan does not have any operating activity for AT1 receptors but has AT1 receptors much stronger (20,000 times) than the AT2 receptor.
Valsartan does not inhibit ACE, also known as Kinase H, which has the effect of converting Ang.i to ang.II and degenerating Bradykinin. Because it does not work on ACE and does not activate Bradykinin or P, Ang.II antagonists are unable to cause cough.
In the Valsartan clinical trials compared to a ACE inhibitor showing a significantly less dry cough ratio (2.6% compared to 7.9% corresponding to P
The use of valsartan for hypertension patients leads to hypotension without affecting the heart rate.
On most patients, after taking a single dose, anti -hypertension effect is achieved within 2 hours and maximum hypotension is achieved within 4-6 hours. Anti -hypertension effect is maintained for more than 24 hours after taking the drug. In the process of repeating drugs, the maximum level of reducing blood pressure at any dose is achieved within 2-4 weeks and is maintained during the long -term treatment. If coordinated with hydrochlorothiazid, it is possible to achieve significant lower blood pressure.
The sudden stop use of Valsartan is not related to the sudden hypertension or clinical side effects. In multi -dose research in hypertension patients, Valsartan has no effects on total cholesterol, triglycerides when hungry, blood sugar when hungry or uric acid.
heart failure
Hemodynamics and neurotrotic hormones in plasma are assessed in patients with heart failure II - IV (according to NYHA classification) with pulmonary capillary pressure ≥ 15 mmHg in 2 short -term studies, prolonged treatment.
In a study, including a long -term treatment patient with ACE inhibitor, single -dose Valsartan and multi -dose treatments combined with valsartan with a transferring inhibitor, improved hemodynamics including pulmonary capillary pressure, internal pulmonary pressure, pulmonary artery pressure in the systolic center. Plasma and plasma aldosteron concentrations decreased after 28 days of treatment.
In the second study, patients only treated with ACE inhibitors at least 6 months before treatment with Valsartan; Valsartan significantly improves the pulmonary capillary pressure, endurance, heart capacity and pulmonary artery pressure in the heart after 28 days of treatment.
In long-term Val-heft research, plasma norepinephrin and sodium peptid brain peptid significantly decreased from the initial concentration of the Valsartan treatment group compared to the placebo group.
Incidence and mortality rates
In multinational research, controlled and random in patients with heart failure treated with valsartan compared to placebo, about the situation of the disease and the mortality rate in patients with heart failure II (62%); III (36%) and IV (2%) according to NYHA's classification with LVEF 2.9 cm/m2. Random study on 5010 patients in 16 countries, valsartan or placebo treatment along with other appropriate medications include ACE inhibitors (93%), diuretic (86%), digoxin (67%) and beta blockers (36%).
Average research time is nearly 2 years.
Valsartan's daily dose is 254 mg for patients with heart failure.Research has come to the first 2 conclusions
All causes of death (time leading to death) and heart failure situation (the start of heart failure) are determined as death, sudden death and regaining consciousness, hospital stay for patients with heart failure, or intravenous medication to enhance heart contractions or vasodilators for 4 hours or not hospitalized.
All causes of death are the same in Valsartan or placebo. The first benefit is to reduce the risk of 27.5% leading to the first hospital for treatment for heart failure. The biggest benefit for patients is no need to be treated with ACE inhibitors or beta blockers. However, the ratio of the place of place of placebo is higher than the group of patients treated in combination with beta blockers, a ACE and Valsartan inhibitors. However, it is very difficult to see the real difference or the changing effects of the two groups of patients have been evaluated.
pharmacokinetic
absorption
After taking Valsartan is quickly absorbed, although the drug's salary is absorbed very different. Valsartan's average bioavailability is 23%. Plasma concentrations in women as well as men.
When using Valsartan with food, the coefficient of variation under the concentration curve over time (AUC) of Valsartan decreases 48%, although after 8 hours of taking medicine, Valsartan concentrations in plasma are similar to those who have eaten or fast.
Despite the decrease in AUC, it does not significantly reduce the effectiveness of the in -treatment, treatment, so Valsartan can be used or not with food.
The pharmacokinetics of Valsartan is linearly corresponding to the test dose. There is no dynamic change of Valsartan when repeated, and accumulates very rarely a dose of a day. Plasma concentrations in women as well as men.Distribution
Valsartan has high plasma protein binding capacity (94 - 97%), mainly serum albumin. The sustainable volume of low circulation (about 17 liters). Valsartan is not much distributed in tissue.
Metabolism
Only 20% of the metabolized valsartan dose. Hydroxy metabolites are found in plasma with low concentrations (
Elimination
Valsartan has a dynamic decomposition according to the exponent coefficient (t ½/2α
Average time to reach the peak concentration and the half -life of Valsartan in patients with heart failure as well as in healthy volunteers are corresponding to each other. The value of AUC and CMAX increases with linear lines and corresponds to the rate of treatment increase (40 to 160 mg twice a day). The average accumulation rate is about 1.7. The clearance coefficient of Valsartan is approximately 4.5 liters/hour. Age also does not change the clearance coefficient of patients with heart failure.
Special group
The elderly: Valsartan's body poisoning is observed in some older people in young people. However, this has no clinical significance.
Periodic impairment: It is thought that the drug excreted through the kidney only accounts for 30% of the total plasma clearance coefficient, and there is no association between the kidney function and the body poisoning of Valsartan. Therefore, the adjustment of the dose in patients with renal failure is unnecessary. No studies have shown that Valsartan can be eliminated by separation because Valsartan is strongly connected to plasma proteins.
Liver functional decline: About 70% of the absorption drug is excreted in biliary tract mainly in a constant form. Valsartan does not undergo biological changes, as predicted, the body poisoning due to Valsartan is not related to the level of liver functional impairment. It is not necessary to adjust the dose of valsartan for patients with liver disability due to the cause of the liver and not bile.
Before taking Savi Valsartan 80 medicine for hypertension, myocardial infarction (3 blisters x 10 tablets)
How to use
Savi Valsartan 80 drugs are used orally, during or outside meals. Drink whole tablets with water. Do not chew, crush or break. Should take medicine at the same time of the day.
Dosage
High blood pressure
The recommended dose of Valsartan is 80 mg/day/once, regardless of racism, age or gender.
In patients with unsatisfactory blood pressure, daily dose may increase to 160 mg or 320 mg depending on the response of the patient.
Children: Adjust the dose by weight. Maximum dose of 320 mg.
after myocardial infarction
In the patient, clinically stabilized, therapy can start as soon as 12 hours after myocardial infarction. The starting dose is 20 mg x 2 times/day, the dose will be increased gradually to a maximum dose of 160 mg x 2 times/day. The last dose depends on the response and tolerance of each patient.
heart failure
The initial dose recommended by Valsartan is 40 mg × 2 times/day.
Increase the dose every 2 weeks from 80 - 160 mg × 2 times daily to the highest dose depending on the patient's tolerance.
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 overdose? If you are new to medication, you should cause vomiting. On the other hand, the common treatment is to conduct intravenous veins of physiological saline solution. Dialysis cannot exclude Valsartan.
What to do when forgetting 1 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 Savi Valsartan 80, you may experience unwanted effects (ADR).
Common, ADR> 1/100
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
Savi Valsartan 80 contraindications in the following cases:
Precautions when using
Hemorrhage:
It is not recommended to share Valsartan with potassium supplements, potassium -saving diuretic or drugs that increase blood potassium (such as heparin). Blood potassium should be checked in Valsartan users.
Renal failure:
No dose adjustment for patients with renal impairment. However, in severe cases (creatinine clearance ratio
Hepatic failure:
Be cautious when using Valsartan in mild and medium liver failure.
Salt loss and/or fluid loss:
In patients with salt loss and/or severe loss of epidemic, if high doses of diuretics, hypotension may occur symptomatic blood pressure in some rare cases after initially treated with valsartan. Salt loss and/or fluid loss should be treated before treatment with Valsartan, for example by reducing diuretics. If the blood pressure occurs, the patient should be left in the back, and if necessary, the veins of the physiological saline solution may be transmitted. The treatment can be continued when the blood pressure is stable.
Kidney artery stenosis:
Using Valsartan for 12 secondary hypertension patients due to one -sided renal artery stenosis does not cause any changes in dynamic acupuncture points, serum creatinine or acupuncture urea (bun - blood urea nitrogen). However, because other drugs affect the renin-analiotensin-aldosteron system may increase serum blood urea and creatinine in patients with kidney stenosis on both sides or one side, it is necessary to monitor as a safety measure.
kidney transplantation:
No experience using Valsartan in this object.
primary Aldosteron:
Do not use valsartan.
Mitral valve stenosis and aortic valve, hypertrophic myocardial disease:
Be cautious when using Valsartan.
after myocardial infarction:
Be cautious when using and should evaluate kidney function regularly.
heart failure:
Be cautious when using and should evaluate kidney function regularly.
The ability to drive and operate machinery
Because the drug has side effects such as headache and dizziness, it must be very careful when using Valsartan for drivers and operating machinery.
Pregnancy
must not be used for pregnant women for more than 3 months. Notify the doctor if you have a plan to get pregnant or suspect pregnancy.
Breastfeeding period Drug interaction
Need to notify your doctor if you are in use or have recently used the following drugs because of the risk of interaction:
Storage
In a dry place, avoid light, temperature below 30 ° C.
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