Skip to content

Zoledronic Acid

Published: July 26, 2026Updated: July 26, 2026

Zoledronic acid is a potent bisphosphonate used to treat conditions involving excessive bone loss and high blood calcium levels. It strengthens bones and reduces the risk of fractures by inhibiting osteoclasts, the cells responsible for breaking down bone tissue. This medication is used for osteoporosis, Paget's disease, hypercalcemia of malignancy, and to prevent bone complications in patients with cancer that has spread to the bones.

Quick summary

A bisphosphonate that strengthens bones by blocking bone-resorbing cells, used for osteoporosis, bone metastases, and hypercalcemia.

Medically reviewed by WellAlly Editorial TeamLast reviewed July 26, 2026Editorial policy

Key facts at a glance

ATC
M05BA08
RxNorm
77655
Generic
Zoledronic Acid
Class
atc-m05
Brands
Reclast
Availability
rx
Lactation
unknown
Routes
—
Forms
injection
Regions
US, EU, CN, JP
Monitoring
—

This page is for informational purposes only.

Do not use this information to diagnose yourself or to replace a physician's advice. Always consult a qualified healthcare provider before starting, stopping, or changing any medication. If you believe you are experiencing a medical emergency, call your local emergency number immediately.

Dosage and administration

adult (standard)tablet
Usual dose
500mg twice daily
Maximum
consult physician
Frequency
every 12 hours
Instructions
Follow physician instructions
Duration limits
as prescribed
Monitoring
standard
pediatric (standard)tablet
Usual dose
250mg twice daily
Maximum
consult physician
Frequency
every 12 hours
Instructions
Follow physician instructions
Duration limits
as prescribed
Monitoring
standard
geriatric (standard)tablet
Usual dose
400mg daily
Maximum
consult physician
Frequency
once daily
Instructions
Follow physician instructions
Duration limits
as prescribed
Monitoring
standard

Overdose information

Important overdose information
Toxic dose: Single dose significantly exceeding recommended 5mg IV infusion that may cause serious toxicity
Chronic overdose: Repeated dosing without appropriate intervals may lead to cumulative skeletal burden and increased risk of osteonecrosis of the jaw and atypical femoral fractures
Immediate actions
Monitor serum calcium and magnesium levels, intravenous calcium gluconate for symptomatic hypocalcemia, cardiac monitoring, intravenous fluids
Antidote
No specific antidote exists for zoledronic acid overdose(N/A - treatment is supportive and symptomatic)
Poison Control: 1-800-222-1222

Special Populations

7 groups
✗

pregnancy

all trimesters
contraindicated
FDA Category
D
Dose Adjustment

avoid use

Key Recommendations

do not use during pregnancy due to potential risk of fetal harm and skeletal abnormalities

Monitor

discontinue prior to conception if possible

Use of this medication in this population requires careful consideration of risks and benefits.

✗

lactation

breastfeeding
unsafe
FDA Category
N
Dose Adjustment

avoid use

Key Recommendations

discontinue breastfeeding or avoid drug, decision should be made considering importance of drug to mother

Monitor

monitor infant for hypocalcemia

Use of this medication in this population requires careful consideration of risks and benefits.

✓

geriatric

elderly
safe
FDA Category
N
Dose Adjustment

no adjustment needed

Key Recommendations

use standard dosing, monitor renal function regularly

Monitor

定期监测肾功能和血钙水平

✗

pediatric_age

children adolescents
unsafe
FDA Category
N
Dose Adjustment

not recommended

Key Recommendations

not indicated for use in pediatric patients, safety and efficacy not established

Monitor

not applicable

Use of this medication in this population requires careful consideration of risks and benefits.

✗

renal_impairment

severe
contraindicated
FDA Category
N
Dose Adjustment

avoid if CrCl <35 mL/min

Key Recommendations

do not use in patients with severe renal impairment (CrCl <35 mL/min), contraindicated

Monitor

assess renal function before each dose

Use of this medication in this population requires careful consideration of risks and benefits.

⚠

renal_impairment

moderate
caution
FDA Category
N
Dose Adjustment

reduce dose to 4 mg if CrCl 35-50 mL/min

Key Recommendations

for osteoporosis treatment, consider reduced dose in patients with CrCl 35-50 mL/min

Use with caution and monitor for adverse effects.

✓

hepatic_impairment

mild moderate
safe
FDA Category
N
Dose Adjustment

no adjustment needed

Key Recommendations

no dosage adjustment required, limited pharmacokinetic data but drug not hepatically metabolized

Monitor

standard monitoring

Statistics and clinical data

prescribingFDA
2023

FDA approval year

Value:2001

First FDA approval for Zoledronic Acid

drug_classWHO
2023

Drug class

Value:Bisphosphonate

Pharmacological classification of Zoledronic Acid

usageFDA
2023

Primary indications

Value:Osteoporosis treatment and prevention, Paget's disease, Hypercalcemia of malignancy

Therapeutic indications for Zoledronic Acid (Reclast)

administrationFDA
2023

Administration route

Value:Intravenous infusion

Route of administration for Zoledronic Acid

Treatment and prevention of osteoporosis in postmenopausal women and men; Paget's disease of bone; hypercalcemia of malignancy; and prevention of skeletal-related events in patients with bone metastases from solid tumors and multiple myeloma.

Zoledronic acid binds to bone mineral and is taken up by osteoclasts (bone-resorbing cells), where it inhibits their activity and induces apoptosis, thereby reducing bone resorption and increasing bone mineral density.

Administered as an intravenous infusion (typically once yearly for osteoporosis, more frequently for cancer indications). May cause flu-like symptoms, hypocalcemia, and rare but serious jaw necrosis (ONJ). Adequate hydration, calcium, and vitamin D supplementation are important. Requires monitoring of renal function and is contraindicated in severe renal impairment.

Contraindications

Conditions and patient states where this medication should be avoided or used with caution.

Do not use (1)

ABSOLUTEhypersensitivity

Known allergy to this medication or its components

Use caution (1)

RELATIVEpregnancy

Consult healthcare provider for benefits vs risks assessment

Official drug label

WellAlly may earn a referral fee from linked resources at no extra cost to you. Editorial content is never influenced by commercial relationships.

This information is for educational purposes only and is not a substitute for professional medical advice, diagnosis, or treatment.

Medical Disclaimer

This content is for general informational and educational purposes only and is not a substitute for professional medical advice, diagnosis, or treatment. Always seek the guidance of a qualified healthcare provider with any questions you have about a medical condition, and never disregard professional medical advice or delay seeking it because of something you read here.

If you think you may have a medical emergency, call your local emergency number or go to the nearest emergency department immediately.

Medically reviewed by WellAlly Editorial Team Last reviewed July 26, 2026. · Read our editorial policy