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Ibandronate

BONIVA

Pronunciation: i-BAN-droe-nayt (bon-EE-va)

Ibandronate ballicule: receptor binding, kinetics and half-life diagram
Mechanism of action: Ibandronate ballicule

What it isFPPS-inhibiting nitrogen bisphosphonate; postmenopausal osteoporosis.

Why this oneMonthly oral or quarterly IV dosing, which suits patients who cannot manage weekly upright dosing.

What limits itVertebral fracture data only — no hip fracture evidence, unlike alendronate and zoledronate. Same esophagitis precautions; avoid below eGFR 30.

Ibandronate molecular structure (skeletal formula)
Molecular structure: Ibandronate

FDA-approved for

FDA label

FDA dosingPopulationStartTargetMax
Postmenopausal osteoporosis (treatment/prevention)Adults150 mg once monthly (same day each month)150 mg once monthly

Renal Not recommended if CrCl <30 mL/min (severe renal impairment)

Hepatic Undefined

Missed dose: if next scheduled day >7 days away, take one tablet next morning then resume; if 1–7 days away, skip and wait for next month

Instructions

Available strengths

Contraindications

Cautions

Adverse reactions

Pregnancy Not indicated in women of reproductive potential; no human data; animal maternal/fetal toxicity

Lactation Not indicated in women of reproductive potential; unknown in human milk (present in rat milk)

Cost

Ibandronate (BONIVA)
What pharmacies pay · NADAC 9/30/26
Strength#/mogeneric $/unitCostPlus
150 mgtabper unit$2.68/eaoffered
3 mg/3 mLinjper unit$52.65/mLnot offered

Generic entry2012

NO BOXED WARNINGS

Principal riskEsophagitis; no hip fracture data

Classes and tags

Clinical profile

Therapeutic safety burden1 / 4
Overdose danger1 / 4
Weight-gain liability0 / 4
Sedation liability0 / 4
QT / Torsades0 / 4
Direct muscarinic antagonism0 / 4
Embryofetal risk2 / 4

Legacy pregnancy categoryC

Defining liabilityGenerally tolerated at therapeutic doses; clinically important risks are agent-specific and increase with interactions or organ impairment.

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