Mavilque Injection (Ibandronic Acid Sodium Monohydrate)
Ibandronate Sodium Monohydrate 3.375mg
Injections · Prescription medication
YuYu Pharmaceutical Co., Ltd.
MFDS item code 201307917 · Notified 2013.06.28 · Insurance code 644501971
Improvement of osteoporosis in postmenopausal women
This medication is used for the treatment of osteoporosis in postmenopausal women.
3 mg is administered by intravenous injection every 3 months over 15-30 seconds.
This medication must be administered intravenously, and great care must be taken to avoid administration into an artery or around a vein, as tissue damage may occur. It should not be used in patients with a known allergy to this medication or any of its components, or in untreated hypocalcemia patients. Use of this medication may result in gastrointestinal adverse reactions such as gastritis, diarrhea, abdominal pain, indigestion, nausea, and constipation. Musculoskeletal pain, joint pain, and muscle pain may occur, and some patients may experience systemic symptoms such as influenza-like symptoms, fatigue, headache, and rash. Rarely, during the administration of this drug, allergic reactions such as vasculitis, hypersensitivity, skin rash, angioedema, and urticaria may occur, so caution is advised. Bisphosphonate medications can cause serious side effects like osteonecrosis of the jaw, so it's advisable to have a dental check-up before taking this medication and to avoid excessive dental treatment during therapy. Long-term use of this medication may lead to atypical fractures in the femur and other bones; if there is pain in the leg or groin, immediate consultation with a healthcare professional is required. This medication can temporarily lower serum calcium levels, so adequate intake of calcium and vitamin D should be ensured before and during treatment, and it should be used only after hypocalcemia is treated. Patients with poor kidney function or taking other medications that may affect the kidneys should have regular check-ups to monitor their condition. It is recommended that pregnant or breastfeeding women do not use this medication, as its safety has not been established. In case of overdose, the renal and hepatic functions may be affected; therefore, immediate monitoring and appropriate treatment at a hospital should be sought if overdose is suspected. This medication should not be mixed with calcium-containing solutions or other intravenous medications and must be administered solely via intravenous injection. After use, do not reuse the syringe or needle, and dispose of them safely, keeping them out of reach of children.
Urticaria, angioedema, facial swelling/edema, hypersensitivity, anaphylactic reactions/shock, Stevens-Johnson syndrome, erythema multiforme, bullous dermatitis, vascular disorders (phlebitis/thromboangiitis), respiratory distress, skin peeling, multiple organ failure, death, acute renal failure, severe allergic reactions, severe edema or urination abnormalities
Not everyone experiences these, and they can vary from person to person.
Store this medication in a sealed container to prevent air or moisture ingress, and it's best to keep it at room temperature between 1°C and 30°C. Proper storage can ensure the safety of the medication's efficacy.
An injection in a colorless, transparent solution contained in a colorless, transparent glass prefilled syringe, equipped with a single-use injection needle.
1 prefilled syringe (3mL/pre-filled syringe)
Even with the same ingredient, strength, dosage form and how it is taken can differ.
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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.
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For anything that needs medical judgment, consult a doctor or pharmacist.
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.