FDA label dced527f-3f3f-ffbb-eb3b-6202d5303a76

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Warnings cross-check#

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warnings and cautions

5 WARNINGS AND PRECAUTIONS • Upper gastrointestinal Adverse Reactions can occur. Instruct patients to follow dosing instructions and discontinue use if new or worsening symptoms occur. ( 5.1 ) • Hypocalcemia may worsen during treatment. Correct hypocalcemia before use. ( 5.2 ) • Severe Bone, Joint, and Muscle Pain may occur. Consider discontinuing use if symptoms develop. ( 5.3 ) • Osteonecrosis of the Jaw has been reported. ( 5.4 ) • Atypical Femur Fractures have been reported. Patients with new thigh or groin pain should be evaluated to rule out a femoral fracture. (5.5) 5.1 Upper Gastrointestinal Adverse Reactions Ibandronate sodium, like other bisphosphonates administered orally, may cause local irritation of the upper gastrointestinal mucosa. Because of these possible irritant effects and a potential for worsening of the underlying disease, caution should be used when ibandronate sodium is given to patients with active upper gastrointestinal problems (such as known Barrett’s esophagus, dysphagia, other esophageal diseases, gastritis, duodenitis or ulcers). Esophageal adverse experiences, such as esophagitis, esophageal ulcers and esophageal erosions, occasionally with bleeding and rarely followed by esophageal stricture or perforation, have been reported in patients receiving treatment with oral bisphosphonates. In some cases, these have been severe and required hospitalization. Physicians should therefore be alert to any signs or symptoms signaling a possible esophageal reaction and patients should be instructed to discontinue ibandronate sodium and seek medical attention if they develop dysphagia, odynophagia, retrosternal pain or new or worsening heartburn. The risk of severe esophageal adverse experiences appears to be greater in patients who lie down after taking oral bisphosphonates and/or who fail to swallow it with the recommended full glass (6 to 8 oz) of water, and/or who continue to take oral bisphosphonates after developing symptoms suggestive of esophageal irritation. Therefore, it is very important that the full dosing instructions are provided to, and understood by, the patient (see DOSAGE AND ADMINISTRATION [2.2]) . In patients who cannot comply with dosing instructions due to mental disability, therapy with ibandronate sodium should be used under appropriate supervision. There have been post-marketing reports of gastric and duodenal ulcers with oral bisphosphonate use, some severe and with complications, although no increased risk was observed in controlled clinical trials. 5.2 Hypocalcemia and Mineral Metabolism Hypocalcemia has been reported in patients taking ibandronate sodium. Treat hypocalcemia and other disturbances of bone and mineral metabolism before starting ibandronate sodium therapy. Instruct patients to take supplemental calcium and vitamin D if their dietary intake is inadequate (see DOSAGE AND ADMINISTRATION [2.3]) . 5.3 Musculoskeletal Pain Severe and occasionally incapacitating bone, joint, and/or muscle pain has been reported in patients taking ibandronate sodium and other bisphosphonates (see ADVERSE REACTIONS [6]) . The time to onset of symptoms varied from one day to several months after starting the drug. Most patients had relief of symptoms after stopping. A subset had recurrence of symptoms when rechallenged with the same drug or another bisphosphonate. Consider discontinuing use if severe symptoms develop. 5.4 Jaw Osteonecrosis Osteonecrosis of the jaw (ONJ), which can occur spontaneously, is generally associated with tooth extraction and/or local infection with delayed healing, and has been reported in patients taking bisphosphonates, including ibandronate sodium. Known risk factors for osteonecrosis of the jaw include invasive dental procedures (e.g., tooth extraction, dental implants, boney surgery), diagnosis of cancer, concomitant therapies (e.g., chemotherapy, corticosteroids, angiogenesis inhibitors), poor oral hygiene, and co-morbid disorders (e.g., periodontal and/or other pre-existing dental disease, anemia, coagulopathy, infection, ill-fitting dentures). The risk of ONJ may increase with duration of exposure to bisphosphonates. For patients requiring invasive dental procedures, discontinuation of bisphosphonate treatment may reduce the risk for ONJ. Clinical judgment of the treating physician and/or oral surgeon should guide the management plan of each patient based on individual benefit/risk assessment. Patients who develop osteonecrosis of the jaw while on bisphosphonate therapy should receive care by an oral surgeon. In these patients, extensive dental surgery to treat ONJ may exacerbate the condition. Discontinuation of bisphosphonate therapy should be considered based on individual benefit/risk assessment. 5.5 Atypical Subtrochanteric and Diaphyseal Femoral Fractures Atypical, low-energy, or low-trauma fractures of the femoral shaft have been reported in bisphosphonate-treated patients. These fractures can occur anywhere in the femoral shaft from just below the lesser trochanter to above the supracondylar flare and are transverse or short oblique in orientation without evidence of comminution. Causality has not been established as these fractures also occur in osteoporotic patients who have not been treated with bisphosphonates. Atypical femur fractures most commonly occur with minimal or no trauma to the affected area. They may be bilateral and many patients report prodromal pain in the affected area, usually presenting as dull, aching thigh pain, weeks to months before a complete fracture occurs. A number of reports note that patients were also receiving treatment with glucocorticoids (e.g., prednisone) at the time of fracture. Any patient with a history of bisphosphonate exposure who presents with thigh or groin pain should be suspected of having an atypical fracture and should be evaluated to rule out an incomplete femur fracture. Patients presenting with an atypical fracture should also be assessed for symptoms and signs of fracture in the contralateral limb. Interruption of bisphosphonate therapy should be considered, pending a risk/benefit assessment, on an individual basis. 5.6 Severe Renal Impairment Ibandronate sodium is not recommended for use in patients with severe renal impairment (creatinine clearance of less than 30 mL/min).

Adverse reactions cross-check#

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adverse reactions

6 ADVERSE REACTIONS The most common adverse reactions (greater than 5%) are back pain, dyspepsia, pain in extremity, diarrhea, headache, and myalgia. ( 6 ) To report SUSPECTED ADVERSE REACTIONS, contact Alvogen, Inc. at 1-866-770-3024 or FDA at 1-800-FDA-1088 or www.fda.gov/medwatch. 6.1 Clinical Trials Experience Because clinical trials are conducted under widely varying conditions, adverse reaction rates observed in the clinical trials of a drug cannot be directly compared to rates in the clinical trials of another drug and may not reflect the rates observed in practice. Treatment and Prevention of Postmenopausal Osteoporosis Monthly Dosing The safety of ibandronate sodium 150 mg as ibandronic acid once monthly in the treatment of postmenopausal osteoporosis was assessed in a two year trial which enrolled 1583 patients aged 54 to 81 years, with 395 patients exposed to ibandronate sodium 2.5 mg as ibandronic acid daily and 396 exposed to ibandronate sodium 150 mg as ibandronic acid monthly. Patients with active or significant pre-existing gastrointestinal disease were excluded from this trial. Patients with dyspepsia or concomitant use of non-steroidal anti-inflammatory drugs, proton pump inhibitors and H2 antagonists were included in this study. All patients received 500 mg calcium plus 400 international units vitamin D supplementation daily. After one year, the incidence of all-cause mortality was 0.3% in both the ibandronate sodium 2.5 mg as ibandronic acid daily group and the ibandronate sodium 150 mg as ibandronic acid monthly group. The incidence of serious adverse events was 5% in the ibandronate sodium 2.5 mg as ibandronic acid daily group and 7% in the ibandronate sodium 150 mg as ibandronic acid monthly group. The percentage of patients who withdrew from treatment due to adverse events was 9% in the ibandronate sodium 2.5 mg as ibandronic acid daily group and 8% in the ibandronate sodium 150 mg as ibandronic acid monthly group. Table 2 lists the adverse events reported in greater than or equal to 2% of patients. Table 2 Adverse Events with an Incidence of at Least 2% in Patients Treated with Ibandronate Sodium 2.5 mg as Ibandronic Acid Daily or 150 mg as Ibandronic Acid Once - Monthly for Treatment of Postmenopausal Osteoporosis Ibandronate sodium 2.5 mg as Ibandronic acid Daily % Ibandronate sodium 150 mg as Ibandronic acid Monthly % Body System/Adverse Event (n=395) (n=396) Vascular Disorders Hypertension 7.3 6.3 Gastrointestinal Disorders Dyspepsia 7.1 5.6 Nausea 4.8 5.1 Diarrhea 4.1 5.1 Constipation 2.5 4 Abdominal Pain a 5.3 7.8 Musculoskeletal and Connective Tissue Disorders Arthralgia 3.5 5.6 Back Pain 4.3 4.5 Pain in Extremity 1.3 4 Localized Osteoarthritis 1.3 3 Myalgia 0.8 2 Muscle Cramp 2 1.8 Infections and Infestations Influenza 3.8 4 Nasopharyngitis 4.3 3.5 Bronchitis 3.5 2.5 Urinary Tract Infection 1.8 2.3 Upper Respiratory Tract Infection 2 2 Nervous System Disorders Headache 4.1 3.3 Dizziness 1 2.3 General Disorders and Administration Site Conditions Influenza-like Illness b 0.8 3.3 Skin and Subcutaneous Tissue Disorders Rash c 1.3 2.3 Psychiatric Disorders Insomnia 0.8 2 a Combination of abdominal pain and abdominal pain upper b Combination of influenza-like illness and acute phase reaction c Combination of rash pruritic, rash macular, rash papular, rash generalized, rash erythematous, dermatitis, dermatitis allergic, dermatitis medicamentosa, erythema and exanthema Gastrointestinal Adverse Events The incidence of adverse events in the ibandronate sodium 2.5 mg as ibandronic acid daily and ibandronate sodium 150 mg as ibandronic acid monthly groups were: dyspepsia (7% vs. 6%), diarrhea (4% vs. 5%), and abdominal pain (5% vs. 8%). Musculoskeletal Adverse Events The incidence of adverse events in the ibandronate sodium 2.5 mg as ibandronic acid daily and ibandronate sodium 150 mg as ibandronic acid monthly groups were: back pain (4% vs. 5%), arthralgia (4% vs. 6%) and myalgia (1% vs. 2%). Acute Phase Reactions Symptoms consistent with acute phase reactions have been reported with bisphosphonate use. Over the two years of the study, the overall incidence of acute phase reaction symptoms was 3% in the ibandronate sodium 2.5 mg as ibandronic acid daily group and 9% in the ibandronate sodium 150 mg as ibandronic acid monthly group. These incidence rates are based on the reporting of any of 33 acute-phase reaction like symptoms within 3 days of the monthly dosing and lasting 7 days or less. Influenza like illness was reported in no patients in the ibandronate sodium 2.5 mg as ibandronic acid daily group and 2% in the ibandronate sodium 150 mg as ibandronic acid monthly group. Ocular Adverse Events Two patients who received ibandronate sodium 150 mg as ibandronic acid once-monthly experienced ocular inflammation, one was a case of uveitis and the other scleritis. One hundred sixty (160) postmenopausal women without osteoporosis participated in a 1 year, double-blind, placebo-controlled study of ibandronate sodium 150 mg as ibandronic acid once-monthly for prevention of bone loss. Seventy-seven subjects received ibandronate sodium and 83 subjects received placebo. The overall pattern of adverse events was similar to that previously observed. 6.2 Postmarketing Experience The following adverse reactions have been identified during postapproval use of ibandronate sodium. Because these reactions are reported voluntarily from a population of uncertain size, it is not always possible to reliably estimate their frequency or establish a causal relationship to drug exposure. Hypersensitivity Allergic reactions including anaphylactic reaction/shock with fatalities, angioedema, bronchospasm, asthma exacerbations, rash, Stevens-Johnson syndrome, erythema multiforme, and dermatitis bullous have been reported (see CONTRAINDICATIONS [4]) . Hypocalcemia Hypocalcemia has been reported in patients treated with ibandronate sodium (see WARNINGS AND PRECAUTIONS [5.2]) . Musculoskeletal Pain Bone, joint, or muscle pain (musculoskeletal pain), described as severe or incapacitating, has been reported (see WARNINGS AND PRECAUTIONS [ 5.3] ) . Jaw Osteonecrosis Osteonecrosis of the jaw and other oro-facial sites, including the external auditory canal, have been reported in patients treated with ibandronate sodium (see WARNINGS AND PRECAUTIONS [5.4]) . Atypical Femoral Shaft Fracture Atypical, low-energy, or low-trauma fractures of the femoral shaft (see WARNINGS AND PRECAUTIONS [ 5.5 ]) .

adverse reactions table

<table border="1" cellspacing="0" width="100%"><tbody><tr><td valign="bottom"/><td align="center" valign="bottom"><content styleCode="bold"> Ibandronate sodium 2.5 mg as Ibandronic acid Daily % </content></td><td align="center" valign="bottom"><content styleCode="bold">Ibandronate sodium 150 mg as Ibandronic acid Monthly %</content></td></tr><tr><td valign="bottom"><content styleCode="bold">Body System/Adverse Event</content></td><td align="center" valign="bottom"><content styleCode="bold">(n=395)</content></td><td align="center" valign="bottom"><content styleCode="bold">(n=396)</content></td></tr><tr><td valign="bottom"><content styleCode="bold">Vascular Disorders</content></td><td valign="bottom"/><td valign="bottom"/></tr><tr><td valign="bottom">Hypertension</td><td align="center" valign="bottom">7.3</td><td align="center" valign="bottom">6.3</td></tr><tr><td valign="bottom"><content styleCode="bold">Gastrointestinal Disorders</content></td><td valign="bottom"/><td valign="bottom"/></tr><tr><td valign="bottom">Dyspepsia</td><td align="center" valign="bottom">7.1</td><td align="center" valign="bottom">5.6</td></tr><tr><td valign="bottom">Nausea</td><td align="center" valign="bottom">4.8</td><td align="center" valign="bottom">5.1</td></tr><tr><td valign="bottom">Diarrhea</td><td align="center" valign="bottom">4.1</td><td align="center" valign="bottom">5.1</td></tr><tr><td valign="bottom">Constipation</td><td align="center" valign="bottom">2.5</td><td align="center" valign="bottom">4</td></tr><tr><td valign="bottom">Abdominal Pain<sup>a</sup></td><td align="center" valign="bottom">5.3</td><td align="center" valign="bottom">7.8</td></tr><tr><td valign="bottom"><content styleCode="bold">Musculoskeletal and Connective Tissue Disorders</content></td><td valign="bottom"/><td valign="bottom"/></tr><tr><td valign="bottom">Arthralgia</td><td align="center" valign="bottom">3.5</td><td align="center" valign="bottom">5.6</td></tr><tr><td valign="bottom">Back Pain</td><td align="center" valign="bottom">4.3</td><td align="center" valign="bottom">4.5</td></tr><tr><td valign="bottom">Pain in Extremity</td><td align="center" valign="bottom">1.3</td><td align="center" valign="bottom">4</td></tr><tr><td valign="bottom">Localized Osteoarthritis</td><td align="center" valign="bottom">1.3</td><td align="center" valign="bottom">3</td></tr><tr><td valign="bottom">Myalgia</td><td align="center" valign="bottom">0.8</td><td align="center" valign="bottom">2</td></tr><tr><td valign="bottom">Muscle Cramp</td><td align="center" valign="bottom">2</td><td align="center" valign="bottom">1.8</td></tr><tr><td valign="bottom"><content styleCode="bold">Infections and Infestations</content></td><td valign="bottom"/><td valign="bottom"/></tr><tr><td valign="bottom">Influenza</td><td align="center" valign="bottom">3.8</td><td align="center" valign="bottom">4</td></tr><tr><td valign="bottom">Nasopharyngitis</td><td align="center" valign="bottom">4.3</td><td align="center" valign="bottom">3.5</td></tr><tr><td valign="bottom">Bronchitis</td><td align="center" valign="bottom">3.5</td><td align="center" valign="bottom">2.5</td></tr><tr><td valign="bottom">Urinary Tract Infection</td><td align="center" valign="bottom">1.8</td><td align="center" valign="bottom">2.3</td></tr><tr><td valign="bottom">Upper Respiratory Tract Infection</td><td align="center" valign="bottom">2</td><td align="center" valign="bottom">2</td></tr><tr><td valign="bottom"><content styleCode="bold">Nervous System Disorders</content></td><td valign="bottom"/><td valign="bottom"/></tr><tr><td valign="bottom">Headache</td><td align="center" valign="bottom">4.1</td><td align="center" valign="bottom">3.3</td></tr><tr><td valign="bottom">Dizziness</td><td align="center" valign="bottom">1</td><td align="center" valign="bottom">2.3</td></tr><tr><td valign="bottom"><content styleCode="bold">General Disorders and Administration Site Conditions</content></td><td valign="bottom"/><td valign="bottom"/></tr><tr><td valign="bottom">Influenza-like Illness<sup>b</sup></td><td align="center" valign="bottom">0.8</td><td align="center" valign="bottom">3.3</td></tr><tr><td valign="bottom"><content styleCode="bold">Skin and Subcutaneous Tissue Disorders</content></td><td valign="bottom"/><td valign="bottom"/></tr><tr><td valign="bottom">Rash<sup>c</sup></td><td align="center" valign="bottom">1.3</td><td align="center" valign="bottom">2.3</td></tr><tr><td valign="bottom"><content styleCode="bold">Psychiatric Disorders</content></td><td valign="bottom"/><td valign="bottom"/></tr><tr><td valign="bottom">Insomnia</td><td align="center" valign="bottom">0.8</td><td align="center" valign="bottom">2</td></tr></tbody></table>