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Published on: 8/18/2026
Long-term bisphosphonate use can suppress bone turnover so much that it raises the risk of atypical femur fractures and jaw osteonecrosis, which is why doctors often pause treatment after three to five years. During that pause, a blood test called CTX (C-terminal telopeptide) measures how actively bone is breaking down, helping your doctor confirm the drug has worn off and decide when protection is fading and treatment should resume. Timing, fasting status, and your fracture risk all change how the result should be read, and there are several important factors to consider before assuming a holiday is safe for you. See below to understand more about target CTX ranges, monitoring intervals, and the warning signs that mean a break should end early.
If you are unsure whether your bone health symptoms, thigh or groin pain, or dental changes warrant a closer look, a free, instant, online symptom check can help you organize what you are feeling in minutes and point you toward the right next step and the right questions for your doctor.
Last reviewed for medical accuracy: 08/18/2026
Bisphosphonates are a mainstay in treating osteoporosis and reducing fracture risk. But long-term use isn’t always risk-free. Over time, your doctor may suggest a “bisphosphonate holiday” to balance benefits and potential side effects. Here’s why taking a break matters, how CTX (C-telopeptide) guides your care, and what you can expect during bisphosphonate holiday duration and monitoring.
A bisphosphonate holiday refers to a planned pause in medications such as alendronate (Fosamax), risedronate (Actonel), ibandronate (Boniva) or zoledronic acid (Reclast).
Reasons for a holiday
Typical holiday duration
Avoiding unnecessary anxiety
• Holidays follow evidence-based guidelines, not random pauses
• You’ll still be monitored closely to catch any changes in bone health
CTX (C-terminal telopeptide of type I collagen) is a blood test that measures how quickly bone breaks down. Higher CTX levels mean faster bone turnover; lower levels suggest slowed turnover.
Why CTX matters during a holiday
• CTX below target range
– Indicates slow bone turnover
– Suggests it’s safe to stay off bisphosphonates
• CTX within target range
– Steady bone remodeling
– Continue monitoring every 6–12 months
• CTX above target range
– Faster bone loss
– Consider resuming treatment
Target ranges vary by lab but generally:
Always discuss your specific target with your doctor.
It’s unlikely you’ll develop serious complications overnight. Still, stay alert to:
If you experience any of these, speak to your doctor right away—or consider a free, online symptom check, using the doctor approved Ubie Symptom Checker.
Benefits of continuing bisphosphonates beyond 3–5 years
Risks of prolonged use
Your doctor weighs:
While off bisphosphonates, focus on lifestyle and nutrition:
• Calcium and vitamin D
– Aim for 1,000–1,200 mg calcium daily (diet + supplements)
– Maintain vitamin D ≥ 30 ng/mL
• Weight-bearing exercise
– Walking, jogging, dancing, or strength training 3–4 times/week
• Fall prevention
– Improve home safety (grab bars, remove loose rugs)
– Use supportive shoes and vision checks
• Healthy habits
– Avoid smoking and limit alcohol
– Ensure adequate protein intake (0.8–1.2 g/kg body weight)
Your doctor may recommend restarting bisphosphonates if you:
Open dialogue with your healthcare team helps you feel confident:
Staying proactive and informed ensures you get the best of both worlds: continuing fracture protection without unnecessary risks. Always talk to your doctor before making any changes to your medication plan. And if you ever experience symptoms that could be serious or life-threatening, seek immediate medical attention or call emergency services.
(References)
* Sawatari Y, Marx RE. Bisphosphonates and bisphosphonate induced osteonecrosis. Oral Maxillofac Surg Clin North Am. 2007 Nov;19(4):487-98, v-vi. doi: 10.1016/j.coms.2007.07.003. PMID: 18088900.
* Chubb SAP, Vasikaran SD. Measurement and Clinical Utility of βCTX in Serum and Plasma. Adv Clin Chem. 2017;81:97-134. doi: 10.1016/bs.acc.2017.01.003. Epub 2017 Feb 16. PMID: 28629592.
* Bindon B, Adams W, Balasubramanian N, Sandhu J, Camacho P. OSTEOPOROTIC FRACTURES DURING BISPHOSPHONATE DRUG HOLIDAY. Endocr Pract. 2018 Feb;24(2):163-169. doi: 10.4158/EP171975.OR. Epub 2017 Nov 16. PMID: 29144808.
* Glendenning P, Chubb SAP, Vasikaran S. Clinical utility of bone turnover markers in the management of common metabolic bone diseases in adults. Clin Chim Acta. 2018 Jun;481:161-170. doi: 10.1016/j.cca.2018.03.009. Epub 2018 Mar 12. PMID: 29544749.
* Ilyas Z, Camacho PM. Rare adverse effects of bisphosphonate therapy. Curr Opin Endocrinol Diabetes Obes. 2019 Dec;26(6):335-338. doi: 10.1097/MED.0000000000000501. PMID: 31567423.
* Reid IR, Billington EO. Drug therapy for osteoporosis in older adults. Lancet. 2022 Mar 12;399(10329):1080-1092. doi: 10.1016/S0140-6736(21)02646-5. PMID: 35279261.
* McDonough A, Malomo K, Brennan F, Fallon N, Steen G, Maher N, O'Carroll C, Walsh JB, Lannon R, McCarroll K. Treatment Challenges When Stopping Denosumab. Ir Med J. 2022 Mar 16;115(3):567. Epub 2022 Mar 16. PMID: 35532944.
* Wang M, Wu YF, Girgis CM. Bisphosphonate Drug Holidays: Evidence From Clinical Trials and Real-World Studies. JBMR Plus. 2022 Jun;6(6):e10629. doi: 10.1002/jbm4.10629. Epub 2022 May 24. PMID: 35720669; PMCID: PMC9189912.
* Salmoral A, Peris P, López Medina C, Flórez H, Barceló M, Pascual Pastor M, Ros I, Grados D, Aguado P, García S, López L, Gifre L, Cerdá D, Aguilar FJ, Panero B, Costa E, Casado E, Hernández B, Martínez Ferrer A, Graña J, Gómez I, Guañabens N, OsteoResSer Working Group of the Spanish Society of Rheumatology. Bisphosphonate drug holidays in osteoporosis according to fracture risk profile. Osteoporos Int. 2025 Feb;36(2):245-254. doi: 10.1007/s00198-024-07309-9. Epub 2024 Dec 3. PMID: 39623217.
* Mohamed A, Fuad U, Abdelazim M, Elasad A, Bhamidipati P. Bisphosphonate-Related Atypical Femoral Fractures: A Comprehensive Review. Cureus. 2025 Nov;17(11):e96208. doi: 10.7759/cureus.96208. Epub 2025 Nov 6. PMID: 41356924; PMCID: PMC12681184.
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