Medication info
Maxdis Tablet

Maxdis Tablet

OTC medicationTablet경구
Ingredient · strength
Calcium Carbonate›750mg / 1 tabletCholecalciferol Concentrate Powder›10mg / 1 tablet
Manufacturer / importer
한국코러스(주)
Appearance
Green oval film-coated tablet
Packaging
30 tablets/bottle, 90 tablets/bottle, 500 tablets/bottle
Approval status
Active

MFDS item code 201605694 · Notified 2016.09.28 · Insurance code 647204250

Summary

Main use
Prevention of bone disorders (hypoplasia, rickets) and improvement of calcium deficiency
Who takes it
Adults · Children
Adult dose
Adults should take 1 tablet once a day.
Child dose
Children aged 8 years and older should take 1 tablet once a day.

Ingredients

Manufacturer
한국코러스(주)

Efficacy & effects

Prevention of bone disorders (hypoplasia, rickets) and improvement of calcium deficiency

  • Bone
  • dental hypoplasia
  • rickets
  • calcium deficiency
View approved original text

Vitamin D is especially needed during pregnancy and lactation, in growing children, and in older adults. The vitamin D included in this medication helps maintain bone and dental health and promotes development. It is also effective in preventing rickets. This medication can be used to maintain and strengthen bone health in cases of calcium deficiency or when additional calcium is required. Therefore, this medication is used to improve bone health and growth through the supplementation of vitamin D and calcium.

How to take

Adult dose

Adults should take 1 tablet once a day.

Child dose

Children aged 8 years and older should take 1 tablet once a day.

Precautions

This medication should not be taken by patients with hypercalcemia (high calcium levels in the blood), patients with sarcoidosis (a condition characterized by inflammation of various organs of the body), or patients with renal disease. Additionally, individuals who are allergic to this medication or its components, infants under 12 months of age, patients with kidney stones, or those with severe renal dysfunction should not take this medication. Because this medication contains lactose, individuals with lactose intolerance or genetic lactose enzyme deficiency should avoid it. While taking this medication, it is advisable not to take it concurrently with drugs such as phosphates, calcium salts, oral tetracycline antibiotics, or antacids. Infants under 1 year old, patients currently undergoing hospital treatment, children receiving adequate sunlight and normal diets, pregnant women or those who might become pregnant, nursing mothers, premature infants, and patients with heart or circulatory issues must consult a physician, dentist, or pharmacist before taking this medication. Patients with renal impairment, hypoproteinemia, those taking cardiac glycosides, and patients with a history of kidney stones should also consult a healthcare professional before using this medication. This medication contains Tartrazine (Yellow No. 4), and individuals allergic to this component should use caution when taking it. If symptoms such as nausea, vomiting, diarrhea, constipation, hypotension, flushing, irregular heartbeats, or skin rashes occur during treatment, discontinue use immediately and consult a professional. Overdosage may lead to gastrointestinal disturbances, hypernatremia, heart failure, and edema, necessitating caution. Long-term use can result in hypercalcemia or stone disease, so regular testing is necessary. Particularly, taking it with aldosterone antagonists or triamterene may elevate potassium levels in the blood, so caution is required. Adhere strictly to the dosage and administer this medication under the supervision of a guardian when used for children. It is advisable to avoid tea containing tannins, such as green tea or black tea, before and after taking this medication. This medication should be stored out of reach of children, and kept in a cool, dry place away from direct sunlight, sealed tightly. To maintain quality, do not transfer to other containers, and prevent misuse.

Side effects and when to seek care immediately

Mild side effects

  • Nausea
  • vomiting
  • diarrhea
  • constipation
  • hypotension
  • flushing
  • irregular heartbeats
  • skin rashes
  • hypernatremia
  • congestive heart failure
Show 1 more
  • edema (swelling)

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

Interactions

Drug interactions

This medication should not be taken concurrently with phosphates, calcium salts, oral tetracycline preparations, or antacids. If taken with cardiac glycosides, aldosterone antagonists, or triamterene, consult a doctor or pharmacist.

Food interactions

This medication should be avoided during and before/after ingestion with tannin-containing teas such as green tea and black tea.

Storage

This medication should be stored in a tightly sealed container to prevent air ingress and kept at room temperature between 1 to 30 degrees Celsius for safety. Storing it this way helps maintain the medication's effectiveness for a longer period.

Appearance and packaging

Appearance

Green oval film-coated tablet

Package unit

30 tablets/bottle, 90 tablets/bottle, 500 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.