Medication info
Cantonnel Tablet 35 mg (Risedronate Sodium)

Cantonnel Tablet 35 mg (Risedronate Sodium)

Prescription medicationTabletOral
Ingredient · strength
Risedronate Sodium›35mg / 1 tablet
Manufacturer / importer
AhnGuk Pharmaceutical Co., Ltd.
Appearance
Pale orange oval film-coated tablet
Packaging
4 tablets/PTP
Approval status
Active

MFDS item code 200801812 · Notified 2008.02.14

Summary

Main use
Treatment of osteoporosis in postmenopausal women and men; prevention of osteoporosis in postmenopausal women
Who takes it
Adults · Children
Adult dose
1. Adults : Administer 35 mg of risedronate sodium orally once weekly. 2. Older adults : No dosage adjustment is necessary in older adults (over 60 years of age), because the bioavailability and pharmacodynamics of this medication are similar to those in younger people. 4. Patients with renal impairment : No dosage adjustment is necessary in patients with a creatinine clearance of 30 mL/min or greater. This medication is contraindicated in patients with severe renal impairment and a creatinine clearance of less than 30 mL/min. ○ Food interferes with the absorption of this medication. To ensure adequate absorption, take it at least 30 minutes before breakfast, or at least 2 hours before or after consuming food or beverages at any time of day. To help this medication reach the stomach easily and reduce the possibility of esophageal irritation, take it while upright with an adequate amount of plain water (170 ∼ 230 mL). Taking it with other beverages, including mineral water, may reduce its absorption. Do not chew or suck this medication because of the possibility of oropharyngeal ulceration. Patients should not lie down for at least 30 minutes after taking it. ○ If a patient forgets to take the medication on the scheduled day, take it the next morning when remembered. Resume the next dose on the originally scheduled day. Do not take 2 tablets on the same day.
Child dose
The safety and efficacy of this medication in children under 18 years of age have not been established.

Ingredients

Manufacturer
AhnGuk Pharmaceutical Co., Ltd.

Efficacy & effects

Treatment of osteoporosis in postmenopausal women and men; prevention of osteoporosis in postmenopausal women

  • Osteoporosis
View approved original text

This medication is used for the treatment and prevention of osteoporosis in postmenopausal women and men. Osteoporosis is a condition that weakens bones, making them more susceptible to fractures, so this medicine can help improve bone health.

How to take

Adult dose

1. Adults : Administer 35 mg of risedronate sodium orally once weekly. 2. Older adults : No dosage adjustment is necessary in older adults (over 60 years of age), because the bioavailability and pharmacodynamics of this medication are similar to those in younger people. 4. Patients with renal impairment : No dosage adjustment is necessary in patients with a creatinine clearance of 30 mL/min or greater. This medication is contraindicated in patients with severe renal impairment and a creatinine clearance of less than 30 mL/min. ○ Food interferes with the absorption of this medication. To ensure adequate absorption, take it at least 30 minutes before breakfast, or at least 2 hours before or after consuming food or beverages at any time of day. To help this medication reach the stomach easily and reduce the possibility of esophageal irritation, take it while upright with an adequate amount of plain water (170 ∼ 230 mL). Taking it with other beverages, including mineral water, may reduce its absorption. Do not chew or suck this medication because of the possibility of oropharyngeal ulceration. Patients should not lie down for at least 30 minutes after taking it. ○ If a patient forgets to take the medication on the scheduled day, take it the next morning when remembered. Resume the next dose on the originally scheduled day. Do not take 2 tablets on the same day.

Child dose

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

Precautions

This medication may irritate the gastrointestinal mucosa, so individuals with diseases of the esophagus, stomach, or duodenum should exercise particular caution. It is important to take this medicine with a sufficient amount of water, and not to lie down for a certain period after taking it. If there are problems with the esophagus or symptoms of swallowing difficulty occur, use should be discontinued immediately and a physician consulted. Individuals with specific diseases, pregnant women, or those with severely impaired kidney function should not take this medicine. Additionally, those with allergies to lactose or colorants contained in this medication should also be cautious. It’s important to ensure adequate intake of calcium and vitamin D while taking this medicine and to take supplements as directed by a physician if necessary. This medication has minimal drug interactions; however, it may interfere with the absorption of other drugs such as calcium or antacids, so a time gap should be maintained between doses. Rarely, serious side effects such as unusual bone fractures or jaw necrosis may occur with long-term use, so any unusual symptoms require immediate consultation with a physician. Pregnant or nursing women are advised to avoid taking this medication, and should consult a doctor if necessary. The safety in children has not been established, hence it should not be administered to anyone under 18 years of age. Caution is necessary for overdose as symptoms like hypocalcemia may occur, and appropriate measures should be taken under a physician's guidance. This medication should be stored out of reach of children and kept in its original container.

Side effects

  • esophagitis
  • esophageal ulcer
  • esophageal erosion
  • esophageal obstruction
  • esophageal perforation
  • hemorrhage
  • gastric ulcer
  • duodenal ulcer
  • dyspepsia
  • diarrhea
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  • nausea
  • abdominal pain
  • allergic reactions
  • hypertension
  • peripheral edema
  • arthralgia
  • arthritis
  • fractures
  • joint abnormalities
  • myalgia
  • bone pain
  • dizziness
  • depression
  • insomnia
  • bronchitis
  • sinusitis
  • rhinitis
  • pharyngitis
  • increased coughing
  • rash
  • cataract
  • urinary tract infection
  • Stevens-Johnson syndrome
  • toxic epidermal necrolysis
  • Liddle syndrome
  • angioedema
  • blisters
  • osteonecrosis of the jaw
  • uveitis
  • scleritis
  • iritis
  • liver dysfunction
  • jaundice
  • loss of appetite
  • asthenia
  • heartburn
  • epigastric pain
  • chest discomfort
  • palpitations
  • increased sweating
  • facial flushing
  • burning sensation
  • kidney stones
  • belching
  • hematuria
  • fever
  • ocular pain

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

Storage

This medication should be stored in an airtight container, preferably between 1℃ and 30℃. Proper storage will maintain the drug's effectiveness and prevent deterioration.

Appearance and packaging

Appearance

Pale orange oval film-coated tablet

Package unit

4 tablets/PTP

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.