Bonova 150 mg contains Ibandronic Acid, a potent nitrogen-containing bisphosphonate used for the treatment of postmenopausal osteoporosis. It is specifically indicated to reduce the risk of fractures in patients with low bone mass or a history of osteoporotic fractures.
Osteoporosis is a condition in which bones become fragile and prone to fracture due to reduced bone mass and structural deterioration. Bonova works by inhibiting osteoclast activity, thereby decreasing bone resorption, improving bone mineral density (BMD), and reducing the risk of vertebral and non-vertebral fractures.
রেজিস্টার্ড চিকিৎসকের পরামর্শ অনুযায়ী ঔষধ সেবন করুন
Bisphosphonate preparations
Ibandronic acid selectively binds to hydroxyapatite in bone, targeting osteoclasts—the cells responsible for bone resorption. It inhibits osteoclast activity without affecting their recruitment or bone formation. In postmenopausal women, Bonova reduces the elevated bone turnover rate, leading to a progressive gain in bone mass.
After oral administration, absorption occurs in the upper gastrointestinal tract. Ibandronic acid is either rapidly taken up by bone tissue or excreted unchanged in the urine. Its high potency allows for flexible dosing, including monthly administration, providing effective fracture risk reduction with convenience and adherence benefits.
Bonova 150 mg is indicated for:
Treatment of postmenopausal osteoporosis to reduce fracture risk
Patients with low bone mass (T-score ≤ -2.0 SD) and a history of osteoporotic fracture
Patients with severely reduced bone mass (T-score ≤ -2.5 SD) even without prior fractures
Recommended Dose: One 150 mg film-coated tablet once monthly
Take on the same date each month
Swallow the tablet whole with a full glass of plain water (180–240 ml)
Take 60 minutes before the first food, drink, or other oral medication, including calcium or supplements
Remain upright (sitting or standing) for at least 60 minutes after administration
Do not chew or suck the tablet to prevent oropharyngeal irritation
If a dose is missed: Take it the following morning unless the next scheduled dose is within 7 days, then skip and continue the original schedule
Patients should also maintain adequate calcium and vitamin D intake to maximize therapeutic benefit.
Hypersensitivity to ibandronic acid or excipients
Uncorrected hypocalcemia
Abnormalities of the esophagus delaying emptying (e.g., stricture, achalasia)
Inability to sit or stand upright for 60 minutes after dosing
Common side effects may include:
Dyspepsia, nausea, diarrhea, abdominal pain
Muscle aches, headaches, dizziness
Rare but serious adverse effects:
Esophagitis, esophageal ulcers, erosions, or strictures
Osteonecrosis of the jaw (ONJ), particularly in patients undergoing dental procedures or with cancer
Correct hypocalcemia and other metabolic bone disturbances before therapy
Use with caution in patients with active upper gastrointestinal conditions (e.g., ulcers, gastritis, Barrett’s esophagus)
Monitor for esophageal irritation; discontinue if dysphagia, odynophagia, or retrosternal pain occurs
Caution when used concurrently with NSAIDs due to additive gastrointestinal risk
Adequate calcium and vitamin D intake is essential
Calcium supplements, antacids, and multivalent cation-containing medications may reduce absorption; wait at least 60 minutes
No significant interactions with tamoxifen, hormone replacement therapy, melphalan/prednisolone, or H2-antagonists
Eliminated unchanged via renal excretion, minimal drug-drug interaction risk
Pregnancy: Use only if benefits outweigh risks; Category C
Lactation: Use caution; unknown excretion in human milk
Pediatrics: Safety and efficacy not established in patients <18 years
Elderly: No dose adjustment needed
Renal Impairment: No adjustment for creatinine clearance ≥30 ml/min
Store below 30°C, in a dry place, protected from light and moisture. Keep out of reach of children.
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