Medication info
Fosalong Plus D Tablet

Fosalong Plus D Tablet

Prescription medicationTablet경구
Ingredient · strength
Sodium Alendronate Hydrate›91.37mg / 1 tabletCholecalciferol Concentrate Powder›53.33mg / 1 tablet
Manufacturer / importer
신풍제약(주)
Appearance
White to light yellow oblong tablet
Packaging
4 tablets (4 tablets/PTP x 1)
Approval status
Active

MFDS item code 201401931 · Approved 2014.04.21 · Insurance code 648507170

Summary

Main use
Improvement of osteoporosis in postmenopausal women and men
Who takes it
Adults · Children
Adult dose
1 tablet (70 mg/2800 IU or 70 mg/5600 IU) of this medication should be taken once a week in the morning at least 30 minutes before intake of food, beverages, or other medications with a sufficient amount of water. Do not lie down for at least 30 minutes after taking and before the first intake of food. It should not be taken before bed or upon waking. If a dose is missed, take 1 tablet of this medication the next morning.
Child dose
Pediatric and adolescent (under 18 years old): Safety and efficacy have not been established.

Ingredients

Manufacturer
신풍제약(주)

Efficacy & effects

Improvement of osteoporosis in postmenopausal women and men

  • Osteoporosis
View approved original text

This medication is used for the treatment of osteoporosis in postmenopausal women and men.

How to take

Adult dose

1 tablet (70 mg/2800 IU or 70 mg/5600 IU) of this medication should be taken once a week in the morning at least 30 minutes before intake of food, beverages, or other medications with a sufficient amount of water. Do not lie down for at least 30 minutes after taking and before the first intake of food. It should not be taken before bed or upon waking. If a dose is missed, take 1 tablet of this medication the next morning.

Child dose

Pediatric and adolescent (under 18 years old): Safety and efficacy have not been established.

Precautions

This medication can irritate the gastrointestinal mucosa, causing upper gastrointestinal adverse reactions such as esophagitis, esophageal ulcers, and esophageal erosions, thus caution is needed during intake. In particular, do not lie down for at least 30 minutes after taking the medication, and it should be taken with a sufficient amount of water to reduce the risk of esophageal irritation. If symptoms such as dysphagia, odynophagia, pain behind the sternum, or heartburn occur, discontinue use immediately and consult a physician. This medication should not be administered to patients with esophageal motility disorders or those who cannot sit upright or stand for more than 30 minutes, to patients with hypersensitivity to the drug's components, to patients with hypocalcemia, or to patients with certain genetic metabolic disorders. While taking this medication, adverse reactions such as indigestion, abdominal pain, nausea, constipation, diarrhea, musculoskeletal pain, headache, dizziness, and taste disturbances may occur, so caution is required. This medication should be taken with a gap from calcium supplements and antacids, and the risk of gastrointestinal adverse reactions may increase when used in conjunction with aspirin. During pregnancy, there may be risks to the fetus, so it should be administered only after consulting a physician, and caution is also needed for nursing mothers. It is not recommended for use in children, and it is not advisable to administer to elderly patients or those with severely impaired renal function. In case of overdose, hypocalcemia, gastrointestinal adverse reactions, etc. may occur, so immediate contact with a medical institution is necessary, and inducing vomiting should be avoided while maintaining an upright position. This medication should be stored out of the reach of children, and transferring to another container should be avoided.

Side effects and when to seek care immediately

Serious side effects

Hives, severe swelling (angioedema), esophagitis, esophageal erosions, esophageal ulcers, and rarely esophageal strictures or perforations, severe allergic reactions, Stevens-Johnson syndrome, toxic epidermal necrolysis, symptoms of hypocalcemia, severe edema, severe skin adverse reactions, severe cutaneous reactions, severe neurological symptoms (seizures, confusion, etc.), reports have included dizziness.

Mild side effects

Abdominal pain, nausea, indigestion, constipation, diarrhea, flatulence, acid reflux, esophageal ulcers, vomiting, dysphagia, abdominal bloating, gastritis, musculoskeletal (bone, muscle, or joint) pain, muscle cramps, headache, dizziness, taste disturbance, rash, itching, hair loss, nasopharyngitis

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

Storage

This medication is sensitive to air and moisture, so it should be stored in a tightly sealed container. It should be stored at room temperature between 1°C and 30°C, and kept in a location protected from direct light to maintain its efficacy.

Appearance and packaging

Appearance

White to light yellow oblong tablet

Package unit

4 tablets (4 tablets/PTP x 1)

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.