Medication info

Seviterra Tablet 5/40 mg

Prescription medicationTablet경구Expired
Ingredient · strength
Amlodipine Besylate›6.944mg / 1 tabletOlmesartan Medoxomil›40mg / 1 tablet
Manufacturer / importer
(주)테라젠이텍스
Appearance
Light yellow round film-coated tablets
Packaging
30 tablets/PTP [10 tablets/PTP x3]
Approval status
Expired

MFDS item code 202002847 · Approved 2020.04.22

This product's status changed to Expired on 2025.04.22. It may no longer be sold, so consult a doctor or pharmacist before taking it.

Summary

Main use
Improvement of blood pressure control in essential hypertension
Who takes it
Adults · Children
Adult dose
This medication is administered once daily, 1 tablet, with or without food, preferably at the same time each day (e.g., morning). The maximum dose is 10/40 mg. The recommended doses are as follows: - 5/20 mg: Administered to patients whose blood pressure is not adequately controlled by monotherapy with either amlodipine 5 mg or olmesartan medoxomil 20 mg. - 10/20 mg
Child dose
The safety and efficacy of this medication in pediatric patients under 18 years of age have not been established.

Ingredients

Manufacturer
(주)테라젠이텍스

Efficacy & effects

Improvement of blood pressure control in essential hypertension

  • Essential hypertension
View approved original text

This medication is used to effectively improve blood pressure in patients with essential hypertension whose blood pressure is not adequately controlled by monotherapy with amlodipine or olmesartan medoxomil. Uncontrolled hypertension can increase the risk of cardiovascular diseases, so this medication helps stabilize blood pressure for better health management. Consistent use and regular blood pressure monitoring can maximize therapeutic effects. This medication plays a significant role in blood pressure control and contributes to the prevention of cardiovascular complications. Therefore, this medication can be used to maintain stable blood pressure levels in the treatment of essential hypertension.

How to take

Adult dose

This medication is administered once daily, 1 tablet, with or without food, preferably at the same time each day (e.g., morning). The maximum dose is 10/40 mg. The recommended doses are as follows: - 5/20 mg: Administered to patients whose blood pressure is not adequately controlled by monotherapy with either amlodipine 5 mg or olmesartan medoxomil 20 mg. - 10/20 mg

Child dose

The safety and efficacy of this medication in pediatric patients under 18 years of age have not been established.

Precautions

This medication can cause serious harm to the fetus and newborn if taken during the second and third trimesters of pregnancy, and should be discontinued immediately upon confirmation of pregnancy. Patients with allergies to any components of this medication, those who are pregnant or breastfeeding, patients with severely impaired liver or kidney function, specific heart valve diseases, those undergoing biliary obstruction or dialysis, patients in shock, diabetic patients taking certain medications, or those with severely decreased kidney function should not use this medication. Patients with hypotension due to deficiency of fluid or salt should be closely monitored when starting this medication, as their blood pressure may fall sharply; appropriate measures should be taken if hypotension occurs. Patients with severe aortic stenosis should be particularly cautious when taking this medication, as it can cause sudden vasodilation leading to hypotension. In patients with severe coronary artery disease, there is an increased risk of angina or myocardial infarction when taking this medication, and caution is advised. Patients with heart failure should be closely monitored for worsening cardiac function when using this medication. This medication may worsen kidney function in patients with reduced kidney function, and should be used with caution. In patients with impaired liver function, the metabolism of this medication may be slowed, necessitating caution. While taking this medication, side effects such as dizziness, headache, hypotension, gastrointestinal disorders, skin rashes, etc. may occur; if any unusual symptoms arise, immediate consultation with a healthcare professional is advised. During pregnancy, this medication may pose risks to the fetus; therefore, patients who plan to become pregnant or are pregnant should switch to safer alternatives. In breastfeeding patients, this medication may be transferred to breast milk and affect the baby, so it is advisable to stop breastfeeding or discontinue the medication. The safety and efficacy of this medication in children under 18 have not been established, and it is not recommended for use in this population. Elderly patients may experience reduced kidney and liver function, so starting at a low dose and close observation is advisable. In case of overdose, severe hypotension and vascular dilation may lead to heart function issues; immediate emergency treatment is required if symptoms occur. This medication should be stored in a tightly closed container, away from direct sunlight and moisture, out of reach of children. When taking this medication with other drugs, potential interactions may occur, so it is essential to inform healthcare professionals of any current medications.

Side effects and when to seek care immediately

Serious side effects

Hives, severe swelling (edema), difficulty breathing, respiratory distress, symptoms of shortness of breath, angioedema, liver abnormalities (jaundice) related symptoms, severe skin adverse reactions (severe rash, blisters, skin peeling, mucosal pain in mouth/eyes), severe neurological symptoms (severe headache, seizures, confusion, visual disturbances, paralysis), severe edema or urinary abnormalities (significant reduction in urine output, generalized severe edema, high blood pressure)

Mild side effects

  • Dizziness
  • headache
  • drowsiness
  • paresthesia
  • reduced sensation
  • palpitations
  • rapid pulse
  • hypotension
  • orthostatic hypotension
  • cough
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  • nausea
  • vomiting
  • dyspepsia
  • diarrhea
  • constipation
  • dry mouth
  • upper abdominal pain
  • rash
  • muscle tension
  • limb pain
  • low back pain
  • increased urination
  • erectile dysfunction
  • peripheral edema
  • swelling
  • pitting edema
  • fatigue
  • weakness
  • facial swelling
  • decreased blood potassium
  • increased blood creatinine
  • increased blood uric acid
  • increased gamma-glutamyl transferase.

Not everyone experiences these, and they can vary from person to person.

Storage

This medication should be stored in a tightly closed container to protect it from air and moisture. It is important to maintain a storage temperature between 1 and 30 degrees Celsius.

Appearance and packaging

Appearance

Light yellow round film-coated tablets

Package unit

30 tablets/PTP [10 tablets/PTP x3]

Same-ingredient medicines

Even with the same ingredient, strength, dosage form and how it is taken can differ.

Even with the same ingredient, the dose and directions can differ by strength and dosage form. Talk to a doctor or pharmacist before switching from a medication you are already taking.

Questions about this medicine

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For anything that needs medical judgment, consult a doctor or pharmacist.

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This drug information is based on data provided by the Korea Ministry of Food and Drug Safety.
Consult a doctor or pharmacist for accurate dosage, administration, and usage instructions.