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|Alendronate Sodium/Cholecalciferol |
Drugs search, click the first letter of a drug name: | A | B | C | D | E | F | G | H | I | J | K | L | M | N | O | P | Q | R | S | T | U | V | W | X | Y | Z | 1 | 2 | 3 | 4 | 5 | 6 | 8 | 9 Home Alendronate Sodium / CholecalciferolPronouncation: (a-LEN-droe-nate SO-dee-um/KOE-le-kal-SIF-er-ole)Class: Biophosphonate combination Trade Names: Mechanism of ActionPharmacologyInhibits bone resorption and increases bone density. Indications and UsageTreatment of osteoporosis in postmenopausal women; treatment to increase bone mass in men with osteoporosis. ContraindicationsAbnormalities of the esophagus that delay esophageal emptying (eg, achalasia, stricture); inability to stand or sit upright for at least 30 min; hypocalcemia; hypersensitivity to any component of the product. Dosage and AdministrationAdultsPO One 70 mg/2,800 unit tablet once weekly. General Advice
Storage/StabilityStore at 59° to 89°F. Protect from moisture and light. Drug InteractionsAntacids, calcium supplementsAlendronate absorption may be reduced; take alendronate at least 30 min before other medications. Anticonvulsants, cimetidine, thiazidesMay increase cholecalciferol catabolism. AspirinIncidence of upper GI adverse reactions may be increased in patients taking more than 10 mg of alendronate daily. Bile acid sequestrants (eg, cholestyramine, colestipol), mineral oil, olestra, orlistatMay impair cholecalciferol absorption. NSAIDsUse with caution because of potential GI irritation. Laboratory Test InteractionsNone well documented. Adverse ReactionsCNSHeadache (3%); asthenia, dizziness, malaise, vertigo (postmarketing). DermatologicPhotosensitivity, pruritus, rash, Stevens-Johnson syndrome, toxic epidermal necrolysis (postmarketing). EENTEpiscleritis, scleritis, uveitis (postmarketing). GIAbdominal pain (7%); dyspepsia, nausea (4%); constipation, diarrhea, flatulence, gastroesophageal reflux disease (3%); acid regurgitation, esophageal ulcer (2%); abdominal distention, dysphagia, vomiting (1%); duodenal ulcers, esophageal erosions, esophageal perforation or stricture, esophageal ulcers, esophagitis, gastric ulcers, oropharyngeal ulceration (postmarketing). Lab TestsMild, transient decreases in serum calcium (18%) and phosphate (10%); symptomatic hypocalcemia (postmarketing). MusculoskeletalBone, muscle, or joint pain (4%); myalgia (postmarketing). MiscellaneousFever, hypersensitivity (including urticaria and angioedema), localized osteonecrosis of the jaw often associated with tooth extraction and/or local infection with delayed healing, peripheral edema (postmarketing). PrecautionsPregnancyCategory C. LactationAlendronate: Undetermined. Cholecalciferol: Excreted in breast milk. ChildrenSafety and efficacy not established. GI disordersUse with caution in patients with upper GI problems (eg, duodenitis, dysphagia, esophageal disease, gastritis, ulcers). Hypocalcemia and mineral metabolism (eg, vitamin D deficiency)Correct before starting treatment. NutritionPatients at increased risk of vitamin D deficiency should receive vitamin D supplementation. Renal function impairmentNot recommended in severe renal function impairment (Ccr less than 35 mL/min). OverdosageSymptomsAnorexia, hypercalcemia, hypercalciuria, hypocalcemia, hypophosphatemia, lethargy, nausea, polydipsia, polyuria, upper GI adverse reactions (eg, esophagitis, gastritis, heartburn, ulcer, upset stomach), vomiting, weakness. Patient Information
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