Medication info
Pistastat 2 mg (Pitavastatin Calcium Hydrate)

Pistastat 2 mg (Pitavastatin Calcium Hydrate)

Prescription medicationTablet경구
Ingredient · strength
Pitavastatin Calcium Hydrate›2mg / 1 tablet
Manufacturer / importer
일양약품(주)
Appearance
Very light yellowish-red round film-coated tablet
Packaging
30 tablets/bottle
Approval status
Active

MFDS item code 201103473 · Approved 2011.05.26 · Insurance code 641704160

Summary

Main use
Improvement of hypercholesterolemia and dyslipidemia
Who takes it
Adults
Adult dose
For adults, the usual initial dose is 1-2 mg of pitavastatin calcium once daily. If the LDL cholesterol-lowering effect is insufficient, the dose can be increased up to a maximum of 4 mg per day. Dosage adjustments should be made appropriately at intervals of 4 weeks or more based on LDL cholesterol levels, treatment goals, and the patient's response.

Ingredients

Manufacturer
일양약품(주)

Efficacy & effects

Improvement of hypercholesterolemia and dyslipidemia

  • Primary hypercholesterolemia
  • compound heterozygous familial hypercholesterolemia
  • non-familial hypercholesterolemia
  • mixed dyslipidemia
  • elevated total cholesterol
  • elevated LDL cholesterol
  • elevated apo-B protein
  • elevated triglyceride levels.
View approved original text

This medication is used to assist with dietary therapy in patients with primary hypercholesterolemia and mixed dyslipidemia. It lowers total cholesterol, LDL cholesterol, apo-B protein, and triglyceride levels, thereby reducing the risk of cardiovascular disease. Additionally, it increases HDL cholesterol levels, promoting the function of good cholesterol. Therefore, this medication is effective in improving blood lipid levels and assisting in the maintenance of patient health.

How to take

Adult dose

For adults, the usual initial dose is 1-2 mg of pitavastatin calcium once daily. If the LDL cholesterol-lowering effect is insufficient, the dose can be increased up to a maximum of 4 mg per day. Dosage adjustments should be made appropriately at intervals of 4 weeks or more based on LDL cholesterol levels, treatment goals, and the patient's response.

Precautions

This medication should not be administered to specific patients. For example, individuals allergic to this drug or those with liver function problems, as well as pregnant or breastfeeding women, should not use it. Additionally, children and patients with muscle diseases should also abstain from this medication. Caution is required when using this medication in the presence of renal or liver abnormalities, or when taking certain concomitant medications. Symptoms like muscle pain or weakness may occur, so monitoring is essential. While taking this medication, regular liver function tests and blood tests should be performed, and immediate consultation with a doctor should occur if any abnormal symptoms arise. Muscle-related side effects such as muscle pain, muscle weakness, and rhabdomyolysis may occur, and administration should be halted if any muscle issues are felt. Rarely, side effects like skin rash, itching, indigestion, headache, and dizziness may also occur. This medication may interact with other drugs, so it is essential to inform the healthcare provider about any other medications being taken, especially with cyclosporine or fibrate medications. Elderly patients may experience more frequent side effects due to reduced bodily function, necessitating dosage adjustments and careful monitoring. Women who could become pregnant should confirm their pregnancy status before taking this medication, and should not take it during pregnancy. If pregnancy is confirmed, use must be discontinued immediately. The safety and efficacy in children have not been established, so it is not used in this population. This medication should be stored out of reach of children, preferably in its original packaging.

Side effects and when to seek care immediately

Serious side effects

  • Hives
  • severe swelling (edema)
  • chest tightness
  • difficulty breathing
  • rhabdomyolysis
  • myopathy
  • liver dysfunction
  • jaundice
  • thrombocytopenia
  • severe allergic reactions
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  • liver abnormalities (jaundice)
  • significant edema or urinary issues
  • hypertension
  • chest discomfort
  • renal deterioration
  • severe neurological symptoms
  • paralysis
  • severe respiratory problems.

Mild side effects

  • Abdominal pain
  • rash
  • fatigue
  • itching
  • stiffness
  • drowsiness
  • insomnia
  • headache
  • feeling of heaviness
  • numbness
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  • dizziness
  • thirst
  • indigestion
  • abdominal bloating
  • constipation
  • stomatitis
  • vomiting
  • loss of appetite
  • glossitis
  • nausea
  • gastrointestinal discomfort
  • diarrhea
  • granulocytopenia
  • leukopenia
  • eosinophilia
  • leukocytosis
  • elevated globulin
  • positive Coombs test
  • anemia
  • polyuria
  • decreased aldosterone
  • increased aldosterone
  • increased adrenocorticotropic hormone
  • cortisol.

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

Storage

This medication should be stored in a container that does not allow light and air, and at a temperature between 1 and 30 degrees Celsius. Proper storage will help maintain the medication's effectiveness.

Appearance and packaging

Appearance

Very light yellowish-red round film-coated tablet

Package unit

30 tablets/bottle

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.