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Alendronate

Published: July 22, 2026Updated: July 22, 2026

Alendronate is a bisphosphonate medication used to treat and prevent osteoporosis by reducing bone loss. It works by inhibiting the cells that break down bone (osteoclasts), helping to maintain or increase bone density and reduce fracture risk. This medication is commonly prescribed for postmenopausal women, men with osteoporosis, and patients on long-term corticosteroid therapy.

Quick summary

Alendronate is a bone-strengthening medication that treats osteoporosis by preventing the breakdown of bone tissue.

Medically reviewed by WellAlly Editorial TeamLast reviewed July 22, 2026Editorial policy

Key facts at a glance

ATC
M05BA04
Generic
Alendronate
Class
bisphosphonate
Brands
Fosamax
Availability
rx
Pregnancy
C
Lactation
caution
Half-life (h)
6000
Routes
oral
Forms
tablet
Regions
CN, US, EU, JP
Monitoring
esophageal-irritation, calcium

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
70mg once weekly
Maximum
consult physician
Frequency
once weekly
Instructions
Follow physician instructions
Duration limits
as prescribed
Monitoring
standard
pediatric (standard)tablet
Usual dose
not indicated
Maximum
consult physician
Frequency
not applicable
Instructions
Follow physician instructions
Duration limits
as prescribed
Monitoring
standard
geriatric (standard)tablet
Usual dose
70mg once weekly
Maximum
consult physician
Frequency
once weekly
Instructions
Follow physician instructions
Duration limits
as prescribed
Monitoring
standard

Overdose information

Important overdose information
Toxic dose: Single doses above 1000 mg may cause serious toxicity including severe hypocalcemia, GI distress, and renal impairment
Chronic overdose: Prolonged use leading to osteonecrosis of the jaw, atypical femur fractures, and severe hypocalcemia
Immediate actions
Do not induce vomiting. Administer milk or calcium-containing antacids to bind the drug. Activate charcoal may be considered if presentation is early. IV calcium gluconate for symptomatic hypocalcemia.
Antidote
No specific antidote exists(Treatment is supportive and symptomatic; no antidote can reverse bisphosphonate effects)
Poison Control: 1-800-222-1222

Special Populations

10 groups
✗

pregnancy

first trimester
unsafe
FDA Category
C
Dose Adjustment

avoid if possible

Key Recommendations

avoid use during pregnancy unless benefits outweigh risks to the fetus

Monitor

regular fetal monitoring and ultrasound assessments

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

✗

pregnancy

second trimester
unsafe
FDA Category
C
Dose Adjustment

avoid if possible

Key Recommendations

discontinue therapy if pregnancy occurs; consider alternative treatments

Monitor

regular fetal monitoring

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

✗

pregnancy

third trimester
unsafe
FDA Category
C
Dose Adjustment

avoid if possible

Key Recommendations

do not use near delivery; may affect fetal bone development

Monitor

fetal growth monitoring

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

?

lactation

not applicable
unknown
FDA Category
N
Dose Adjustment

avoid or discontinue breastfeeding

Key Recommendations

not recommended during breastfeeding; decide whether to discontinue drug or breastfeeding

Monitor

monitor infant for any adverse effects

✓

geriatric

over 65 years
safe
FDA Category
N
Dose Adjustment

no dosage adjustment required

Key Recommendations

use standard dosing; monitor renal function periodically

Monitor

regular renal function monitoring, assess for gastrointestinal adverse effects

✗

pediatric_age

under 18 years
unsafe
FDA Category
C
Dose Adjustment

not recommended; do not use

Key Recommendations

safety and efficacy not established in pediatric population

Monitor

not applicable

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

✗

renal_impairment

severe creatinine clearance below 35
unsafe
FDA Category
N
Dose Adjustment

contraindicated

Key Recommendations

do not use in patients with severe renal impairment

Monitor

monitor renal function before and during treatment

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

⚠

renal_impairment

mild moderate creatinine clearance 35 80
caution
FDA Category
N
Dose Adjustment

no dose adjustment needed

Key Recommendations

use with caution; ensure adequate hydration

Monitor

monitor renal function periodically

Use with caution and monitor for adverse effects.

✓

hepatic_impairment

mild moderate
safe
FDA Category
N
Dose Adjustment

no dosage adjustment required

Key Recommendations

no dose adjustment needed for mild to moderate impairment

Monitor

standard monitoring

⚠

alcohol_users

chronic heavy use
caution
FDA Category
N
Dose Adjustment

use with caution

Key Recommendations

limit alcohol consumption; may increase risk of gastrointestinal adverse effects

Monitor

monitor for gastrointestinal complications

Use with caution and monitor for adverse effects.

Statistics and clinical data

prescribingFDA
2023

FDA approval year

Value:1995

Original FDA approval for Alendronate (Fosamax)

drug_classWHO
2023

Drug class

Value:Bisphosphonate

Pharmacological classification of Alendronate

usageFDA
2023

Primary indications

Value:Treatment and prevention of osteoporosis in postmenopausal women and men

Main therapeutic uses of Alendronate

mechanismFDA
2023

Mechanism of action

Value:Inhibits osteoclast-mediated bone resorption

Primary pharmacological mechanism

Treatment and prevention of osteoporosis in postmenopausal women, treatment of osteoporosis in men, treatment of glucocorticoid-induced osteoporosis, and treatment of Paget's disease of bone.

Alendronate binds to bone mineral and is taken up by osteoclasts (bone-resorbing cells), where it inhibits their activity and promotes apoptosis, thereby reducing bone breakdown and helping to maintain bone density.

Must be taken first thing in the morning with plain water on an empty stomach; remain upright for at least 30-60 minutes after taking to prevent esophageal irritation. Common side effects include gastrointestinal symptoms. Rare but serious risks include osteonecrosis of the jaw and atypical femur fractures with long-term use. Calcium and vitamin D supplementation is often recommended alongside treatment.

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

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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 22, 2026. · Read our editorial policy