Medication info
Atomet Extended Release Tablet 20/750 mg

Atomet Extended Release Tablet 20/750 mg

Prescription medicationTablet경구
Ingredient · strength
Metformin Hydrochloride›750mg / 1 tabletAtorvastatin Calcium Hydrate›21.7mg / 1 tablet
Manufacturer / importer
에이치케이이노엔(주)
Appearance
White, double convex, egg-shaped film-coated tablet
Packaging
7 tablets/bottle, 30 tablets/bottle
Approval status
Active

MFDS item code 201801996 · Approved 2018.05.10

Summary

Main use
Efficacy of combination therapy substitution
Who takes it
Adults
Adult dose
This medication is administered once a day in adults, in conjunction with the evening meal. To facilitate the ease of administration for patients taking metformin hydrochloride and atorvastatin calcium hydrate as separate agents, this combination formulation may be used (with the same active ingredient content).

Ingredients

Manufacturer
에이치케이이노엔(주)

Efficacy & effects

Efficacy of combination therapy substitution

View approved original text

This medication is used as a combination therapy for patients who need to take metformin hydrochloride and atorvastatin calcium hydrate together.

How to take

Adult dose

This medication is administered once a day in adults, in conjunction with the evening meal. To facilitate the ease of administration for patients taking metformin hydrochloride and atorvastatin calcium hydrate as separate agents, this combination formulation may be used (with the same active ingredient content).

Precautions

This medication may rarely cause a serious metabolic disorder known as lactic acidosis; if symptoms occur, consult a physician immediately. Additionally, caution is required when used with insulin or sulfonylureas due to the risk of hypoglycemia. If symptoms of muscle pain or myopathy occur, discontinue use immediately and inform healthcare professionals. Patients with severely impaired renal function or certain conditions such as acute myocardial infarction or heart failure should not use this medication. The use of this medication should be temporarily suspended before and after examinations using iodine contrast agents, and should be resumed only after renal function has been confirmed to be normal. This medication is contraindicated for patients allergic to any components in the drug, patients with specific metabolic acidosis, pregnant or breastfeeding women, and children under 10 years old. Irregular meals, excessive exercise, and excessive alcohol consumption may increase the risk of side effects from this medication, so caution is necessary. During treatment, it is important to regularly check kidney and liver function and verify vitamin B12 levels. This medication should be avoided with alcohol consumption, and interactions may occur when used with other medications, so consult with a physician or pharmacist. If symptoms such as muscle pain, weakness, or fever occur, inform healthcare professionals immediately and undergo examination. Women who are pregnant or planning to become pregnant should not take this medication and should use appropriate contraceptive methods. Elderly patients may have decreased kidney function, so dosage adjustments and regular monitoring are necessary. In case of overdose, seek appropriate treatment at a medical institution immediately, and keep out of reach of children.

Side effects and when to seek care immediately

Serious side effects

Hives, severe swelling (edema), tightness in the chest, difficulty breathing, cold sweat, pallor, severe rash with high fever, blisters, skin peeling, pain in the mouth/eye mucosa, yellowing of skin or eyes (jaundice), profound lethargy, sudden and severe headache, thunderclap headache, seizures, confusion, vision abnormalities, paralysis, markedly reduced urine output, generalized severe swelling with hypertension, severe allergic reactions.

Mild side effects

  • Nausea
  • diarrhea
  • dyspepsia
  • abdominal pain
  • constipation
  • gastritis
  • gastrointestinal disorders
  • vomiting
  • irritable bowel syndrome
  • hypoglycemia
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  • liver function abnormalities
  • muscle pain
  • back pain
  • lower abdominal pain
  • erosive gastritis
  • hemorrhoids
  • sensitive teeth
  • nasopharyngitis
  • upper respiratory tract infections
  • herpes simplex
  • liver abscess
  • chronic otitis media
  • fluid imbalance
  • hypomagnesemia
  • muscle pain
  • tendon rupture
  • benign prostatic hyperplasia
  • conjunctival injection
  • blurred vision
  • dizziness
  • facial spasms
  • hypertension

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

Storage

This medication should be stored in a tightly closed container to avoid exposure to air or moisture. It is best to maintain storage temperatures between 1 and 30 degrees Celsius.

Appearance and packaging

Appearance

White, double convex, egg-shaped film-coated tablet

Package unit

7 tablets/bottle, 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.