Actonel with Calcium
"The U.S. Food and Drug Administration today warned patients and health care providers about the possible risk of atypical thigh bone (femoral) fracture in patients who take bisphosphonates, a class of drugs used to prevent and treat osteoporosis."...
Actonel with Calcium
Actonel with Calcium (risedronate sodium with calcium carbonate) is indicated for the treatment and prevention of osteoporosis in postmenopausal women.
Treatment of Osteoporosis
In postmenopausal women with osteoporosis, Actonel increases BMD and reduces the incidence of vertebral fractures and a composite endpoint of nonvertebral osteoporosis-related fractures (see Clinical Studies). Osteoporosis may be confirmed by the presence or history of osteoporotic fracture, or by the finding of low bone mass (for example, at least 2 SD below the premenopausal mean).
Prevention of Osteoporosis
Actonel may be considered in postmenopausal women who are at risk of developing osteoporosis and for whom the desired clinical outcome is to maintain bone mass and to reduce the risk of fracture.
Factors such as family history of osteoporosis, previous fracture, smoking, BMD (at least 1 SD below the premenopausal mean), high bone turnover, thin body frame, Caucasian or Asian race, and early menopause are associated with an increased risk of developing osteoporosis and fractures. The presence of these risk factors may be important when considering the use of Actonel for prevention of osteoporosis.
The safety and effectiveness of Actonel with Calcium (risedronate sodium with calcium carbonate) for the treatment of osteoporosis are based on clinical data of three years duration. The optimal duration of use has not been determined. All patients on bisphosphonate therapy should have the need for continued therapy re-evaluated on a periodic basis.
DOSAGE AND ADMINISTRATION
Treatment and Prevention of Postmenopausal Osteoporosis (see INDICATIONS AND USAGE)
One 35 mg Actonel tablet orally, taken once-a-week (Day 1 of the 7-day treatment cycle)
Actonel should be taken at least 30 minutes before the first food or drink of the day other than water. Actonel should not be taken at the same time as other medications, including calcium.
To facilitate delivery to the stomach, Actonel should be swallowed while the patient is in an upright position and with a full glass of plain water (6 to 8 oz). Patients should not lie down for 30 minutes after taking the medication (see PRECAUTIONS, General). Actonel is not recommended for use in patients with severe renal impairment (creatinine clearance < 30 mL/min). No dosage adjustment is necessary in patients with a creatinine clearance ≥ 30 mL/min or in the elderly.
One 1250 mg calcium carbonate tablet (500 mg elemental calcium) orally, taken with food daily on each of the remaining six days (Days 2 through 7 of the 7-day treatment cycle)
The recommended total (diet and otherwise) daily calcium intake in postmenopausal women is 1200 mg of elemental calcium. If patients need calcium in excess of that provided by Actonel with Calcium (risedronate sodium with calcium carbonate) , this should be taken with food at a separate time of day.
Patients should receive additional vitamin D if dietary intake is inadequate (see PRECAUTIONS, General). Co-administration of calcium tablets and calcium-, aluminum-, and magnesium-containing medications may interfere with the absorption of Actonel (see DRUG INTERACTIONS).
Actonel with Calcium (risedronate sodium with calcium carbonate) is not recommended for use in patients with severe renal impairment (creatinine clearance < 30 mL/min). No dosage adjustment is necessary in patients with a creatinine clearance ≥ 30 mL/min or in the elderly.
Actonel® with Calcium (risedronate sodium with calcium carbonate) is supplied in blister packages containing a 28-day course of therapy.
Four Actonel Tablets:
35 mg film-coated, oval, orange tablets with RSN on 1 face and 35 mg on the other
Twenty-four Calcium Carbonate Tablets, USP:
1250 mg calcium carbonate (equivalent to 500 mg elemental calcium) film-coated, oval, light blue tablets with NE 2 engraved on both faces
Store at 20° - 25° C (68° - 77° F); excursions permitted between 15° - 30° C (59° - 86° F) [see USP Controlled Room Temperature].
Actonel manufactured by: Warner Chilcott Puerto Rico LLC, Manati, Puerto Rico 00674 or Norwich Pharmaceuticals, Inc., North Norwich, NY 13814. Calcium manufactured by: Norwich Pharmaceuticals, Inc. North Norwich, NY 13814. Marketed by: Warner Chilcott (US), LLC Rockaway, NJ 07866 1-800-521-8813. . Revised January 2011This monograph has been modified to include the generic and brand name in many instances.
Last reviewed on RxList: 3/18/2011
Additional Actonel with Calcium Information
- Actonel with Calcium Drug Interactions Center: risedronate-calcium oral
- Actonel with Calcium Side Effects Center
- Actonel with Calcium in detail including Side Effects and Drug Images
- Actonel with Calcium Overview including Precautions
- Actonel with Calcium FDA Approved Prescribing Information including Dosage
Actonel with Calcium - User Reviews
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