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利塞钙片|Actonel w/ Calcium(Risedronate/Calcium Tablets)

2011-12-23 00:25:06  作者:新特药房  来源:中国新特药网天津分站  浏览次数:847  文字大小:【】【】【
简介: 英文药名: Actonel w/ Calcium(Risedronate/Calcium Tablets) 中文参考药名: 利塞钙片 生产厂家: Warner Chilcott Laboratories 利塞钙片名称和成分 通用名称: 利塞膦酸钠片英文名称: Risedron ...

英文药名: Actonel w/ Calcium(Risedronate/Calcium Tablets)

中文参考药名: 利塞钙片

生产厂家: Warner Chilcott Laboratories

药品介绍

FDA批准利塞膦酸钠(Risedronate sodium/Actonel)新适应证

日前,美国食品药品管理局(FDA)批准了美国宝洁公司利塞膦酸钠(Risedronate sodium/Actonel)35毫克片剂的一个重要新适应证,即1周1次口服1片治疗男子骨质疏松症以提高其骨质水平。

在此之前,利塞膦酸钠的该剂量方案也已被批准预防和治疗绝经后妇女的骨质疏松症。

利塞膦酸钠是主要依据一项包括284例骨质疏松症男子的两年期安慰剂对照、双盲、多中心临床试验数据而获批上述新适应证的。

试验证实,接受利塞膦酸钠治疗的患者在第6、12和24个月时测量的腰椎骨矿物密度均获统计学显著性改善,同时他们的骨周转标志物水平也呈统计学显著性降低。

临床试验中,其副反应及发生率都与安慰剂相似,最常报告的相关症状有便秘、背痛、关节痛、流感和鼻咽炎等。

利塞钙片名称和成分

通用名称: 利塞膦酸钠片
英文名称: Risedronate Sodium Tablets
本品主要成份为利塞膦酸钠
化学名称: 2-(3-吡啶基)-1-羟基乙烷-1,1-双膦酸单钠盐二倍半水合物。
本品为白色薄膜衣片,除去包衣后显白色。
适应症

本品用于治疗和预防绝经后妇女的骨质疏松症。
规格

5mg(以C7H10NNaO7P2计)
用法用量

口服用药,需至少餐前30分钟直立位服用,一杯(200ml左右)清水送服,服药后30分钟内不宜卧床。用量为一日一次,一次5mg(一片)。
如果您有任何疑问,请遵医嘱。
不良反应

1、消化系统 可引起上消化道紊乱,表现为吞咽困难、食道炎、食道或胃溃疡,还可以引起腹泻、腹痛、恶心、便秘等;
其他如流感样综合征、头痛、头晕、皮疹、关节痛等。
禁忌

以下患者禁用
1、已知对本品过敏者;
2、低钙血症患者;
3、30分钟内难以坚持站立或端坐位者。
孕妇及哺乳期妇女用药

孕妇用药的安全有效性尚未确立,除非疾病本身对母子的危害性更大并无其他更安全药物替代时,才在妊娠期使用本品。
本品对哺乳婴儿有严重的不良反应,哺乳期妇女应停药或停止哺乳。
儿童用药

儿童用药的安全有效性尚未确立。
老年患者用药

临床试验资料表明,老年人和年轻人在服用本品时无安全性和有效性上的差异,但不排除老年人个体对本品具有高敏性。
注意事项

1、服药后2小时内,避免食用高钙食品(例如牛奶或奶制品)以及服用补钙剂或含铝、镁等的抗酸药物。
2、不宜与阿司匹林或非甾体抗炎药同服。
3、重度肾功能损害者慎用本品。
4、饮食中钙、维生素D摄入不足者,应加服这些药品。
5、勿嚼碎或吸吮本品。
药物相互作用

没有有关本品特殊的药物间相互作用的报道。本品不被代谢,也不诱导或抑制肝细胞色素酶P450。
钙剂/抗酸剂 本品与钙剂、抗酸剂以及含二价阳离子的口服制剂同服,会影响本品的吸收。
激素替代治疗 如运用得当,本品可与激素联合使用。
阿司匹林/非甾体抗炎药 在5700名病人参加的本品III期临床试验中,31%病人服用阿司匹林,其中24%为规律服用,48%的病人服用了非甾体类抗炎药,其中21%为规律服用,结果显示服用阿司匹林/非甾体抗炎药的病人中,上消化道不良反应的发生率,本品组(24.5%)与安慰剂组(24.8%)相似。
H2-受体阻滞剂和质子泵抑制剂 在上述同一试验中, 21%病人服用了H2-受体阻滞剂和质子泵抑制剂,这些病人中,上消化道副反应的发生率,本品组与安慰剂组相似。
药物过量

过量使用可能会引起血钙、磷下降,还会出现低血钙症状。牛奶或含钙的抗酸剂可以减少本品的吸收,洗胃可以清除未吸收的药物,静脉注射钙制剂,可减轻低血钙症状。
药理毒理

药理作用:
利塞膦酸钠能够与骨中羟磷灰石结合,具有抑制骨吸收的作用。在细胞水平,本品抑制破骨细胞。破骨细胞通常存在于骨表面上,但不具有明显的吸收活性。对大鼠、狗、小猪进行组织形态测定,发现本品可减少骨转换(活化频率,即骨组织重构部位被活化的速率)和骨再塑部位的吸收。
动物试验提示,本品可抑制骨质疏松模型大鼠和小型猪的破骨细胞,抑制骨吸收。大鼠和小猪分别经口给予本品(按体表面积折算,剂量分别为人用剂量5mg/m2 的4和25倍,计算方法下同),骨量和骨生物力学强度呈剂量依赖性增加,骨密度的增加与骨生物力学强度呈现正相关,对骨结构和骨矿化无明显影响。狗经口给予本品(剂量分别为人用剂量的0.35~1.4倍),可促进骨更新单元水平上的骨平衡。狗经口给予本品1mg/kg/天(约为人用剂量的5倍),可延迟骨折愈合。这种作用与其他二膦酸盐化合物相似,但在0.1mg/ kg/天的剂量下不发生。大鼠本品治疗后对骨骼进行组织检查,结果在高剂量(5mg/kg/天,皮下注射)下也没有影响骨矿化,也未出现骨软化。
毒理研究
遗传毒性:本品在沙门氏伤寒菌及大肠杆菌体外回复突变试验(Ames试验)、哺乳动物细胞基因突变试验(CHO/HPRT)、大鼠肝细胞程序外DNA合成试验、大鼠骨髓细胞微核试验中未见基因毒性。CHO细胞染色体裂变试验中,浓度达到细胞毒水平时(>675mcg/ml,存活率6%~7%)出现阳性结果,但在细胞存活率达29%的剂量水平时,未发现染色体损伤。
生殖毒性:雌性大鼠经口给予本品16mg/kg/天(按体表面积折算,相当于人用剂量30mg/天的5.2倍,下同),排卵受到抑制;剂量为7mg/kg/天(相当于人用剂量的2.3倍),着床减少。雄性大鼠经口给予本品40mg/kg/天,可见睾丸和附睾萎缩、炎性细胞浸润;大鼠连续13周经口给予本品16mg/kg/天,也可见睾丸萎缩;犬连续13周经口给予本品8mg/kg/天(相当于人用剂量的8倍),可见中度至重度的精子生成障碍。这些变化随给药剂量的增加和给药时间延长而趋严重。
妊娠期大鼠经口给予本品,剂量≥16mg/kg/天(相当于人用剂量的5.2倍)时,胎鼠成活率降低;在80mg/kg/天的剂量下,胎仔体重下降;在7.1mg/kg/天剂量下,见胸骨或颅骨骨化数明显增高;在≥16mg/kg/天剂量下,胸骨未骨化或骨化不完全均明显增加;在≥3.2mg/kg/天剂量下,可见胚胎腭裂发生率下降,但该发现与临床的相关性尚不清楚。妊娠家兔经口给予本品,剂量达10mg/kg/天(相当于人用剂量的6.7倍)时,未发现对胚胎骨化产生影响,但14窝中有1窝流产,另外1窝早产分娩。
与其他二膦酸类化合物类似,大鼠在交配期与妊娠期给药,剂量低至3.2mg/kg/天(相当于人用剂量的1倍)可致亲代动物分娩期低血钙症和死亡。此外,本品能在大鼠乳汁中分泌。
致癌性:在104周的致癌研究中,大鼠经口给予本品达24mg/kg/天,未发现明显因药物引起的肿瘤。试验中,雄鼠高剂量组(24mg/kg/天)因毒性反应较大,于第93周时停止试验。在大鼠80周的致癌研究中,本品给药剂量达32mg/kg/天时未发现明显因药物引起的肿瘤。
药代动力学

据文献报道,本品的药代动力学特点如下:
吸收 :本品口服后由上消化道迅速吸收,血药浓度达峰时间(Tmax)约为服药后1小时,在一定剂量范围内(单剂量给药:2.5~30mg、多剂量给药:2.5~5mg),吸收呈剂量依赖性。连续用药57天内可达到稳态血浆浓度。利塞膦酸钠片的平均绝对口服生物利用度为0.63%(90%置信限:0.54%~ 0.75%),与食物同服时生物利用度降低。与空腹给药相比,早餐前半小时或晚餐后2小时给药,吸收减少55%;早餐前1小时给药,吸收减少30%。本品在早餐前至少30分钟给药是有效的。
分布:人体平均稳态分布容积为6.3L/kg。人血浆蛋白结合率约为24%。给大鼠和狗静脉注射单剂量14C标记的本品,吸收量的大约60%分布到骨组织,其余随尿液排出,软组织分布极少,大鼠经多次灌胃后,大约有0.001%~0.01%的本品分布到软组织。
代谢: 本品在体内无明显代谢。
清除 口服给药后,吸收量的约一半在24小时内随尿排出,未吸收的药物以原型随粪便排出。其平均肾清除率为105ml/分,与肌酐清除率之间呈线性关系,而无剂量依赖性。终末半衰期(t1/2)达480h,代表本品从骨组织的解离速率。
特殊人群的药代动力学
儿童: 本品尚未在18岁以下患者中进行药代动力学研究。
性别: 本品的口服生物利用度和药代动力学基本上没有性别差异。
老年: 老年患者(>60岁)和年轻患者具有相似的生物利用度,因此老年患者不需调整剂量。
肾功能不全: 本品主要以原形经肾排泄。与肾功能正常的人相比,肌酐清除率约为30ml/分的患者,本品的肾清除率约减少70%。严重肾功能损害(肌酐清除率<30ml/分)的患者慎用本品。肌酐清除率≥30ml/分的患者不需要调整剂量。
肝功能不全: 尚未在肝功能损害的患者中评价过本品的安全性和有效性。

贮藏

密封,凉暗(避光并不超过20℃)处保存。请置于儿童不易拿到处.

规格:
35mg/1250mg*1周用量  (Warner Chilcott 生产) 
35mg/500mg *28 片(Procter & Gamble生产)

ACTONEL® with CALCIUM
(risedronate sodium tablets with calcium carbonate tablets, USP)

DESCRIPTION

ACTONEL with CALCIUM is a co-package product containing ACTONEL (risedronate sodium tablets, 35 mg) for once weekly dosing and calcium carbonate tablets, USP (1250 mg, equivalent to 500 mg elemental calcium) for daily dosing for the remaining 6 days of the week. Each package contains a 28-day course of therapy.

ACTONEL

ACTONEL (risedronate sodium tablets) is a pyridinyl bisphosphonate that inhibits osteoclast-mediated bone resorption and modulates bone metabolism. Each ACTONEL tablet in the ACTONEL with CALCIUM co-package contains the equivalent of 35 mg of anhydrous risedronate sodium in the form of the hemi-pentahydrate with small amounts of monohydrate. The empirical formula for risedronate sodium hemi-pentahydrate is C7H10NO7P2Na •2.5 H2O. The chemical name of risedronate sodium is [1-hydroxy-2-(3-pyridinyl)ethylidene]bis[phosphonic acid] monosodium salt. The chemical structure of risedronate sodium hemi-pentahydrate is the following:

Risedronate sodium is a fine, white to off-white, odorless, crystalline powder. It is soluble in water and in aqueous solutions, and essentially insoluble in common organic solvents.

CALCIUM

The empirical formula for calcium carbonate is CaCO3 and the molecular weight is 100.09.

Calcium carbonate is supplied as a calcium carbonate tablet, USP containing 1250 mg calcium carbonate (equivalent to 500 mg elemental calcium). Calcium carbonate is a fine, white, odorless, tasteless powder. It is stable and non-hygroscopic.

Calcium carbonate is formulated per USP standards to meet disintegration or dissolution, weight, purity, and potency requirements.

Inactive Ingredients:

ACTONEL

Crospovidone, ferric oxide red, ferric oxide yellow, hydroxypropyl cellulose, hydroxypropyl methylcellulose, lactose monohydrate, magnesium stearate, microcrystalline cellulose, polyethylene glycol, silicon dioxide, titanium dioxide.

CALCIUM

Pregelatinized starch, sodium starch glycolate, FD&C Blue #2, magnesium stearate, polyethylene glycol 3350, hypromellose, Opaspray Light Blue, polysorbate 80.

CLINICAL PHARMACOLOGY

ACTONEL

Mechanism of Action:

ACTONEL has an affinity for hydroxyapatite crystals in bone and acts as an antiresorptive agent. At the cellular level, ACTONEL inhibits osteoclasts. The osteoclasts adhere normally to the bone surface, but show evidence of reduced active resorption (e.g., lack of ruffled border). Histomorphometry in rats, dogs, and minipigs showed that ACTONEL treatment reduces bone turnover (activation frequency, i.e., the rate at which bone remodeling sites are activated) and bone resorption at remodeling sites.

Pharmacokinetics:

Absorption:

Absorption after an oral dose is relatively rapid (tmax ~1 hour) and occurs throughout the upper gastrointestinal tract. The fraction of the dose absorbed is independent of dose over the range studied (single dose, 2.5 to 30 mg; multiple dose, 2.5 to 5 mg). Steady-state conditions in the serum are observed within 57 days of daily dosing. Mean absolute oral bioavailability of the 30 mg tablet is 0.63% (90% CI: 0.54% to 0.75%) and is comparable to a solution. The extent of absorption of a 30 mg dose (three 10 mg tablets) when administered 0.5 hours before breakfast is reduced by 55% compared to dosing in the fasting state (no food or drink for 10 hours prior to or 4 hours after dosing). Dosing 1 hour prior to breakfast reduces the extent of absorption by 30% compared to dosing in the fasting state. Dosing either 0.5 hours prior to breakfast or 2 hours after dinner (evening meal) results in a similar extent of absorption. ACTONEL is effective when administered at least 30 minutes before breakfast.

Distribution:

The mean steady-state volume of distribution is 6.3 L/kg in humans. Human plasma protein binding of drug is about 24%. Preclinical studies in rats and dogs dosed intravenously with single doses of [14C] risedronate indicate that approximately 60% of the dose is distributed to bone. The remainder of the dose is excreted in the urine. After multiple oral dosing in rats, the uptake of risedronate in soft tissues was in the range of 0.001% to 0.01%.

Metabolism:

There is no evidence of systemic metabolism of risedronate.

Elimination:

Approximately half of the absorbed dose is excreted in urine within 24 hours, and 85% of an intravenous dose is recovered in the urine over 28 days. Mean renal clearance is 105 mL/min (CV = 34%) and mean total clearance is 122 mL/min (CV = 19%), with the difference primarily reflecting nonrenal clearance or clearance due to adsorption to bone. The renal clearance is not concentration dependent, and there is a linear relationship between renal clearance and creatinine clearance. Unabsorbed drug is eliminated unchanged in feces. Once risedronate is absorbed, the serum concentration-time profile is multi-phasic, with an initial half-life of about 1.5 hours and a terminal exponential half-life of 480 hours. This terminal half-life is hypothesized to represent the dissociation of risedronate from the surface of bone.

CALCIUM

Calcium is a major substrate for mineralization and has an antiresorptive effect on bone. Calcium suppresses PTH secretion and decreases bone turnover. Increased levels of PTH are known to contribute to age-related bone loss, especially at cortical sites, while increased bone turnover is an independent risk factor of fractures.

Pharmacokinetics:

Absorption:

Calcium is released from calcium complexes during digestion in a soluble, ionized form, for absorption from the small intestine. Absorption can be by both passive and active mechanisms. Active absorption of calcium is highly dependent on vitamin D, and vitamin D deficiency decreases the absorption of calcium. As calcium intake increases, the active transfer mechanism becomes saturated and an increasing proportion of calcium is absorbed via passive diffusion. Absorption of calcium carbonate is dose-dependent, with fractional absorption being highest when at doses up to 500 mg. Absorption of calcium is also dependent on pH with reduced absorption in alkaline conditions. The absorption of calcium from calcium carbonate is increased when taken with food.

Distribution:

Approximately 50% of calcium in the serum is in the physiologically active ionized form; about 10% is complexed to phosphate, citrate or other anions. The remaining 40% is bound to proteins, primarily albumin.

Elimination:

Unabsorbed calcium from the small intestine is excreted in the feces. Renal excretion depends largely on glomerular filtration and calcium tubular reabsorption with more than 98% of calcium reabsorbed from the glomerular filtrate. This process is regulated by active vitamin D and PTH.

Special Populations:

ACTONEL

Pediatric:

Risedronate pharmacokinetics have not been studied in patients <18 years of age.

Gender:

Bioavailability and pharmacokinetics following oral administration are similar in men and women.

Geriatric:

Bioavailability and disposition are similar in elderly (>60 years of age) and younger subjects. No dosage adjustment is necessary.

Race:

Pharmacokinetic differences due to race have not been studied.

Renal Insufficiency:

Risedronate is excreted unchanged primarily via the kidney. As compared to persons with normal renal function, the renal clearance of risedronate was decreased by about 70% in patients with creatinine clearance of approximately 30 mL/min. ACTONEL is not recommended for use in patients with severe renal impairment (creatinine clearance <30 mL/min) because of lack of clinical experience. No dosage adjustment is necessary in patients with a creatinine clearance ≥30 mL/min.

Hepatic Insufficiency:

No studies have been performed to assess risedronate's safety or efficacy in patients with hepatic impairment. Risedronate is not metabolized in rat, dog, and human liver preparations. Insignificant amounts (<0.1% of intravenous dose) of drug are excreted in the bile in rats. Therefore, dosage adjustment is unlikely to be needed in patients with hepatic impairment.

CALCIUM

Absorption of calcium from calcium carbonate is poor in patients with achlorhydria unless taken with food.

Gender:

Absorption of calcium from calcium carbonate has not been adequately studied with respect to gender.

Geriatric:

There are no clinically significant differences in bioavailability following administration of 1 g elemental calcium as calcium carbonate between young (20 – 27 years) and elderly (63 – 71 years) females.

Race:

The effect of race on calcium absorption from oral calcium carbonate has not been studied.

Renal Insufficiency:

Renal disease affects calcium homeostasis through its effects on vitamin D metabolism, phosphorus excretion, and PTH. Calcium should be administered cautiously to patients with renal disease (creatinine clearance <30 mL/min) to avoid elevations of the calcium-phosphorus ion product (Ca x Phos) and the development of calcinosis.

Pharmacodynamics:

ACTONEL

Treatment and Prevention of Osteoporosis in Postmenopausal Women:

Osteoporosis is characterized by decreased bone mass and increased fracture risk, most commonly at the spine, hip, and wrist.

The diagnosis can be confirmed by the finding of low bone mass, evidence of fracture on x-ray, a history of osteoporotic fracture, or height loss or kyphosis indicative of vertebral fracture. Osteoporosis occurs in both men and women but is more common among women following menopause. In healthy humans, bone formation and resorption are closely linked; old bone is resorbed and replaced by newly-formed bone. In postmenopausal osteoporosis, bone resorption exceeds bone formation, leading to bone loss and increased risk of bone fracture. After menopause, the risk of fractures of the spine and hip increases; approximately 40% of 50 year-old women will experience an osteoporosis-related fracture during their remaining lifetimes. After experiencing 1 osteoporosis-related fracture, the risk of future fracture increases 5-fold compared to the risk among a non-fractured population.

ACTONEL treatment decreases the elevated rate of bone turnover that is typically seen in postmenopausal osteoporosis. In clinical trials, administration of ACTONEL to postmenopausal women resulted in decreases in biochemical markers of bone turnover, including urinary deoxypyridinoline/creatinine and urinary collagen cross-linked N-telopeptide (markers of bone resorption) and serum bone specific alkaline phosphatase (a marker of bone formation). At the 5 mg dose, decreases in deoxypyridinoline/creatinine were evident within 14 days of treatment. Changes in bone formation markers were observed later than changes in resorption markers, as expected, due to the coupled nature of bone resorption and bone formation; decreases in bone specific alkaline phosphatase of about 20% were evident within 3 months of treatment. Bone turnover markers reached a nadir of about 40% below baseline values by the sixth month of treatment and remained stable with continued treatment for up to 3 years. Bone turnover is decreased as early as 14 days and maximally within about 6 months of treatment, with achievement of a new steady-state that more nearly approximates the rate of bone turnover seen in premenopausal women. In a 1-year study comparing daily versus weekly oral dosing regimens of ACTONEL for the treatment of osteoporosis in postmenopausal women, ACTONEL 5 mg daily and ACTONEL 35 mg once a week decreased urinary collagen cross-linked N-telopeptide by 60% and 61%, respectively. In addition, serum bone-specific alkaline phosphatase was also reduced by 42% and 41% in the ACTONEL 5 mg daily and ACTONEL 35 mg once a week groups, respectively. ACTONEL is not an estrogen and does not have the benefits and risks of estrogen therapy.

As a result of the inhibition of bone resorption, asymptomatic and usually transient decreases from baseline in serum calcium (<1%) and serum phosphate (<3%) and compensatory increases in serum PTH levels (<30%) were observed within 6 months in patients in osteoporosis clinical trials. There were no significant differences in serum calcium, phosphate, or PTH levels between the ACTONEL and placebo groups at 3 years. In a 1-year study comparing daily versus weekly oral dosing regimens of ACTONEL in postmenopausal women, the mean changes from baseline at 12 months were similar between the ACTONEL 5 mg daily and ACTONEL 35 mg once a week groups, respectively, for serum calcium (0.4% and 0.7%), phosphate (-3.8% and -2.6%) and PTH (6.4% and 4.2%).

CALCIUM

Calcium administration decreases the elevated rate of bone turnover typically seen in postmenopausal women with osteoporosis. In randomized, placebo controlled studies in postmenopausal women, calcium administration (500 mg to 1600 mg) decreased biochemical markers of bone turnover, including urine N-telopeptide, urine free pyridinoline (markers of bone resorption), alkaline phosphatase and osteocalcin (markers of bone formation) relative to placebo treated women.

Calcium administration may transiently increase levels of serum calcium with compensatory reductions in serum PTH and an increase in urinary calcium. However, urinary and serum calcium levels usually remain within the normal reference range.

CLINICAL STUDIES

ACTONEL

Treatment of Osteoporosis in Postmenopausal Women:

The fracture efficacy of ACTONEL 5 mg daily in the treatment of postmenopausal osteoporosis was demonstrated in 2 large, randomized, placebo-controlled, double-blind studies that enrolled a total of almost 4000 postmenopausal women under similar protocols. The Multinational study (VERT MN) (ACTONEL 5 mg, n = 408) was conducted primarily in Europe and Australia; a second study was conducted in North America (VERT NA) (ACTONEL 5 mg, n = 821). Patients were selected on the basis of radiographic evidence of previous vertebral fracture, and therefore, had established disease. The average number of prevalent vertebral fractures per patient at study entry was 4 in VERT MN, and 2.5 in VERT NA, with a broad range of baseline bone mineral density (BMD) levels. All patients in these studies received supplemental calcium 1000 mg/day. Patients with low vitamin D levels (approximately 40 nmol/L or less) also received supplemental vitamin D 500 IU/day.

Positive effects of ACTONEL treatment on BMD were also demonstrated in each of 2 large, randomized, placebo-controlled trials (BMD MN and BMD NA) in which almost 1200 postmenopausal women (ACTONEL 5 mg, n = 394) were recruited on the basis of low lumbar spine bone mass (more than 2 SD below the premenopausal mean) rather than a history of vertebral fracture.

ACTONEL 35 mg once a week (n = 485) was shown to be therapeutically equivalent to ACTONEL 5 mg daily (n = 480) in a 1-year, double-blind, multicenter study of postmenopausal women with osteoporosis. In the primary efficacy analysis of completers, the mean increases from baseline in lumbar spine BMD at 1 year were 4.0% (3.7, 4.3; 95% confidence interval [CI]) in the 5 mg daily group (n = 391) and 3.9% (3.6, 4.3; 95% CI) in the 35 mg once a week group (n = 387) and the mean difference between 5 mg daily and 35 mg weekly was 0.1%(-0.42, 0.55; 95% CI). The results of the intent-to-treat analysis with the last observation carried forward were consistent with the primary efficacy analysis of completers. The 2 treatment groups were also similar with regard to BMD increases at other skeletal sites.

Effect on Vertebral Fractures:

Fractures of previously undeformed vertebrae (new fractures) and worsening of pre-existing vertebral fractures were diagnosed radiographically; some of these fractures were also associated with symptoms (i.e., clinical fractures). Spinal radiographs were scheduled annually and prospectively planned analyses were based on the time to a patient's first diagnosed fracture. The primary endpoint for these studies was the incidence of new and worsening vertebral fractures across the period of 0 to 3 years. ACTONEL 5 mg daily significantly reduced the incidence of new and worsening vertebral fractures and of new vertebral fractures in both VERT NA and VERT MN at all time points (Table 1). The reduction in risk seen in the subgroup of patients who had 2 or more vertebral fractures at study entry was similar to that seen in the overall study population.

Table 1   The Effect of ACTONEL on the Risk of Vertebral Fractures
Proportion of Patients
with Fracture (%)a
VERT NA Placebo
n = 678
ACTONEL 5 mg
n = 696
Absolute Risk
Reduction (%)
Relative Risk
Reduction (%)

a Calculated by Kaplan-Meier methodology.

New and Worsening
   0 - 1 Year 7.2 3.9 3.3 49
   0 - 2 Years 12.8 8.0 4.8 42
   0 - 3 Years 18.5 13.9 4.6 33
New
   0 - 1 Year 6.4 2.4 4.0 65
   0 - 2 Years 11.7 5.8 5.9 55
   0 - 3 Years 16.3 11.3 5.0 41
VERT MN Placebo
n = 346
ACTONEL 5 mg
n = 344
Absolute Risk
Reduction (%)
Relative Risk
Reduction (%)
New and Worsening
   0 - 1 Year 15.3 8.2 7.1 50
   0 - 2 Years 28.3 13.9 14.4 56
   0 - 3 Years 34.0 21.8 12.2 46
New
   0 - 1 Year 13.3 5.6 7.7 61
   0 - 2 Years 24.7 11.6 13.1 59
   0 - 3 Years 29.0 18.1 10.9 49
Effect on Osteoporosis-Related Nonvertebral Fractures:

In VERT MN and VERT NA, a prospectively planned efficacy endpoint was defined consisting of all radiographically confirmed fractures of skeletal sites accepted as associated with osteoporosis. Fractures at these sites were collectively referred to as osteoporosis-related nonvertebral fractures. ACTONEL 5 mg daily significantly reduced the incidence of nonvertebral osteoporosis-related fractures over 3 years in VERT NA (8% vs. 5%; relative risk reduction 39%) and reduced the fracture incidence in VERT MN from 16% to 11%. There was a significant reduction from 11% to 7% when the studies were combined, with a corresponding 36% reduction in relative risk. Figure 1 shows the overall results as well as the results at the individual skeletal sites for the combined studies.

Figure 1   Nonvertebral Osteoporosis-Related Fractures, Cumulative Incidence Over 3 Years: Combined VERT MN and VERT NA

Effect on Height:

In the two 3-year osteoporosis treatment studies, standing height was measured yearly by stadiometer. Both ACTONEL and placebo-treated groups lost height during the studies. Patients who received ACTONEL had a statistically significantly smaller loss of height than those who received placebo. In VERT MN, the median annual height change was -1.3 mm/yr in the ACTONEL 5 mg daily group compared to -2.4 mm/yr in the placebo group. In VERT NA, the median annual height change was -0.7 mm/yr in the ACTONEL 5 mg daily group compared to -1.1 mm/yr in the placebo group.

Effect on Bone Mineral Density:

The results of 4 randomized, placebo-controlled trials in women with postmenopausal osteoporosis (VERT MN, VERT NA, BMD MN, BMD NA) demonstrate that ACTONEL 5 mg daily increases BMD at the spine, hip, and wrist compared to the effects seen with placebo. Table 2 displays the significant increases in BMD seen at the lumbar spine, femoral neck, femoral trochanter, and midshaft radius in these trials compared to placebo. Thus, overall ACTONEL reverses the loss of BMD, a central factor in the progression of osteoporosis. In both VERT studies (VERT MN and VERT NA), ACTONEL 5 mg daily produced increases in lumbar spine BMD that were progressive over the 3 years of treatment, and were statistically significant relative to baseline and to placebo at 6 months and at all later time points.

Table 2   Mean Percent Increase in BMD from Baseline in Patients Taking ACTONEL 5 mg or Placebo at Endpointa
VERT MNb VERT NAb BMD MNc BMD NAc
Placebo
n = 323
5 mg
n = 323
Placebo
n = 599
5 mg
n = 606
Placebo
n = 161
5 mg
n = 148
Placebo
n = 191
5 mg
n = 193

a The endpoint value is the value at the study's last time point for all patients who had BMD measured at that time; otherwise the last postbaseline BMD value prior to the study's last time point is used.

b The duration of the studies was 3 years.

c The duration of the studies was 1.5 to 2 years.

* BMD of the midshaft radius was measured in a subset of centers in VERT MN (placebo, n = 222; 5 mg, n = 214) and VERT NA (placebo, n = 310; 5 mg, n = 306)

ND = analysis not done

Lumbar Spine 1.0 6.6 0.8 5.0 0.0 4.0 0.2 4.8
Femoral Neck -1.4 1.6 -1.0 1.4 -1.1 1.3 0.1 2.4
Femoral
Trochanter
-1.9 3.9 -0.5 3.0 -0.6 2.5 1.3 4.0
Midshaft Radius -1.5* 0.2* -1.2* 0.1* ND ND
Histology/Histomorphometry:

Bone biopsies from 110 postmenopausal women were obtained at endpoint. Patients had received daily ACTONEL (2.5 mg or 5 mg) or placebo for 2 to 3 years. Histologic evaluation (n = 103) showed no osteomalacia, impaired bone mineralization, or other adverse effects on bone in ACTONEL-treated women. These findings demonstrate that bone formed during ACTONEL administration is of normal quality. The histomorphometric parameter mineralizing surface, an index of bone turnover, was assessed based upon baseline and post-treatment biopsy samples from 23 patients treated with ACTONEL 5 mg and 21 treated with placebo. Mineralizing surface decreased moderately in ACTONEL-treated patients (median percent change: ACTONEL 5 mg, -74%; placebo, -21%), consistent with the known effects of treatment on bone turnover.

Prevention of Osteoporosis in Postmenopausal Women:

ACTONEL 5 mg daily prevented bone loss in a majority of postmenopausal women (age range 42 to 63 years) within 3 years of menopause in a 2-year, double-blind, placebo-controlled study in 383 patients (ACTONEL 5 mg, n = 129). All patients in this study received supplemental calcium 1000 mg/day. Increases in BMD were observed as early as 3 months following initiation of ACTONEL treatment. ACTONEL 5 mg produced significant mean increases in BMD at the lumbar spine, femoral neck, and trochanter compared to placebo at the end of the study (Figure 2). ACTONEL 5 mg daily was also effective in patients with lower baseline lumbar spine BMD (more than 1 SD below the premenopausal mean) and in those with normal baseline lumbar spine BMD. Bone mineral density at the distal radius decreased in both ACTONEL and placebo-treated women following 1 year of treatment.

 

Figure 2   Change in BMD from Baseline: 2-Year Prevention Study

ACTONEL 35 mg once a week prevented bone loss in postmenopausal women (age range 44 to 64 years) without osteoporosis in a 1-year, double-blind, placebo-controlled study in 278 patients (ACTONEL 35 mg, n = 136). All patients were supplemented with 1000 mg elemental calcium and 400 IU vitamin D per day. The primary efficacy measure was the percent change in lumbar spine BMD from baseline after 1 year of treatment using LOCF (last observation carried forward). ACTONEL 35 mg once a week resulted in a statistically significant mean difference from placebo in lumbar spine BMD of +2.9% (least square mean for risedronate +1.83%; placebo -1.05%). ACTONEL 35 mg once a week also showed a statistically significant mean difference from placebo in BMD at the total proximal femur of +1.5% (risedronate +1.01%; placebo -0.53%), femoral neck of +1.2% (risedronate +0.22%; placebo -1.00%), and trochanter of +1.8% (risedronate +1.07%; placebo -0.74%).

Combined Administration with Hormone Replacement Therapy:

The effects of combining ACTONEL 5 mg daily with conjugated estrogen 0.625 mg daily (n = 263) were compared to the effects of conjugated estrogen alone (n = 261) in a 1-year, randomized, double-blind study of women ages 37 to 82 years, who were on average 14 years postmenopausal. The BMD results for this study are presented in Table 3.

Table 3   Percent Change from Baseline in BMD After 1 Year of Treatment
Estrogen 0.625 mg
n = 261
ACTONEL 5 mg +
Estrogen 0.625 mg
n = 263
Lumbar Spine 4.6± 0.20 5.2± 0.23
Femoral Neck 1.8± 0.25 2.7± 0.25
Femoral Trochanter 3.2± 0.28 3.7± 0.25
Midshaft Radius 0.4± 0.14 0.7± 0.17
Distal Radius 1.7± 0.24 1.6± 0.28
Values shown are mean (± SEM) percent change from baseline.
Histology/Histomorphometry:

Bone biopsies from 53 postmenopausal women were obtained at endpoint. Patients had received ACTONEL 5 mg plus estrogen or estrogen alone once daily for 1 year. Histologic evaluation (n = 47) demonstrated that the bone of patients treated with ACTONEL plus estrogen was of normal lamellar structure and normal mineralization. The histomorphometric parameter mineralizing surface, a measure of bone turnover, was assessed based upon baseline and post-treatment biopsy samples from 12 patients treated with ACTONEL plus estrogen and 12 treated with estrogen alone. Mineralizing surface decreased in both treatment groups (median percent change: ACTONEL plus estrogen, -79%; estrogen alone, -50%), consistent with the known effects of these agents on bone turnover.

ANIMAL PHARMACOLOGY AND/OR TOXICOLOGY

ACTONEL

Risedronate demonstrated potent anti-osteoclast, antiresorptive activity in ovariectomized rats and minipigs. Bone mass and biomechanical strength were increased dose-dependently at oral doses up to 4 and 25 times the human recommended oral dose of 35 mg/week based on surface area, (mg/m2) for rats and minipigs, respectively. Risedronate treatment maintained the positive correlation between BMD and bone strength and did not have a negative effect on bone structure or mineralization. In intact dogs, risedronate induced positive bone balance at the level of the bone remodeling unit at oral doses ranging from 0.35 to 1.4 times the human 35 mg/week dose based on surface area (mg/m2).

In dogs treated with an oral dose of 1 mg/kg/day (approximately 5 times the human 35 mg/week dose based on surface area, mg/m2), risedronate caused a delay in fracture healing of the radius. The observed delay in fracture healing is similar to other bisphosphonates. This effect did not occur at a dose of 0.1 mg/kg/day (approximately 0.5 times the human 35 mg/week dose based on surface area, mg/m2).

The Schenk rat assay, based on histologic examination of the epiphyses of growing rats after drug treatment, demonstrated that risedronate did not interfere with bone mineralization even at the highest dose tested (5 mg/kg/day, subcutaneously), which was approximately 3500 times the lowest antiresorptive dose (1.5 mcg/kg/day in this model) and approximately 8 times the human 35 mg/week dose based on surface area (mg/m2). This indicates that ACTONEL administered at the therapeutic dose is unlikely to induce osteomalacia.

CALCIUM

Published studies have demonstrated that changes in the dietary intake of calcium affect bone growth and skeletal development in animals, as well as bone loss in animal models of estrogen-depletion/ovariectomy and aging.

INDICATIONS AND USAGE

Postmenopausal Osteoporosis:

ACTONEL with CALCIUM 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.

CONTRAINDICATIONS

ACTONEL

  • Hypocalcemia (see PRECAUTIONS, General)
  • Known hypersensitivity to any component of this product
  • Inability to stand or sit upright for at least 30 minutes

CALCIUM

  • Hypercalcemia from any cause including, but not limited to, hyperparathyroidism, hypercalcemia of malignancy, or sarcoidosis.
  • Known hypersensitivity to any component of the product.

WARNINGS

ACTONEL

Bisphosphonates may cause upper gastrointestinal disorders such as dysphagia, esophagitis, and esophageal or gastric ulcer (see PRECAUTIONS).

CALCIUM

See PRECAUTIONS

PRECAUTIONS

General:

ACTONEL

Hypocalcemia and other disturbances of bone and mineral metabolism should be effectively treated before starting ACTONEL therapy. Adequate intake of calcium and vitamin D is important in all patients. ACTONEL is not recommended for use in patients with severe renal impairment (creatinine clearance <30 mL/min).

Bisphosphonates have been associated with gastrointestinal disorders such as dysphagia, esophagitis, and esophageal or gastric ulcers. This association has been reported for bisphosphonates in postmarketing experience, but has not been found in most pre-approval clinical trials, including those conducted with ACTONEL. Patients should be advised that taking the medication according to the instructions is important to minimize the risk of these events. They should take ACTONEL with sufficient plain water (6 to 8 oz) to facilitate delivery to the stomach, and should not lie down for 30 minutes after taking the drug.

Osteonecrosis, primarily in the jaw, has been reported in patients treated with bisphosphonates. Most cases have been in cancer patients undergoing dental procedures such as tooth extraction, but some have occurred in patients with postmenopausal osteoporosis or other diagnoses. Most reported cases have been in patients treated with bisphosphonates intravenously but some have been in patients treated orally.

For patients requiring dental procedures, there are no data available to suggest whether discontinuation of bisphosphonate treatment, prior to the procedure, reduces the risk of osteonecrosis of the jaw. Clinical judgement should guide the management plan of each patient based on individual benefit/risk assessment.

Musculoskeletal Pain:

In postmarketing experience, there have been infrequent reports of severe and occasionally incapacitating bone, joint, and/or muscle pain in patients taking bisphosphonates (see ADVERSE REACTIONS). 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 medication. A subset had recurrence of symptoms when rechallenged with the same drug or another bisphosphonate.

CALCIUM

ACTONEL with CALCIUM should not be used to treat hypocalcemia. Total daily intake of calcium above 1500 mg has not demonstrated additional bone benefits while daily intake above 2000 mg has been associated with increased risk of adverse effects, including hypercalcemia and kidney stones.

Administration of calcium has been associated with a slight increase in the risk of kidney stones.

In patients with a history of kidney stones or hypercalciuria, metabolic assessment to seek treatable causes of these conditions is warranted. If administration of calcium tablets should be needed in these patients, urinary calcium excretion and other appropriate testing should be monitored periodically.

Patients with achlorhydria may have decreased absorption of calcium. Taking calcium with food enhances absorption.

Concomitant use of calcium-containing antacids should be monitored to avoid excessive intake of calcium.

Information for Patients:

ACTONEL

The patient should be informed to pay particular attention to the dosing instructions as clinical benefits may be compromised by failure to take the drug according to instructions. Specifically, ACTONEL should be taken at least 30 minutes before the first food or drink of the day other than water.

To facilitate delivery to the stomach, and thus reduce the potential for esophageal irritation, patients should take ACTONEL while in an upright position (sitting or standing) 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). Patients should not chew or suck on the tablet because of a potential for oropharyngeal irritation.

Patients should be instructed that if they develop symptoms of esophageal disease (such as difficulty or pain upon swallowing, retrosternal pain or severe persistent or worsening heartburn) they should consult their physician before continuing ACTONEL.

Patients should be instructed that if they miss a dose of ACTONEL 35 mg once a week, they should take 1 tablet on the morning after they remember and return to taking 1 tablet once a week, as originally scheduled on their chosen day. Patients should not take 2 tablets on the same day.

Patients should receive supplemental calcium and vitamin D if dietary intake is inadequate (see PRECAUTIONS, General). Calcium supplements or calcium-, aluminum-, and magnesium-containing medications may interfere with the absorption of ACTONEL and should be taken at a different time of the day, as with food.

Weight-bearing exercise should be considered along with the modification of certain behavioral factors, such as excessive cigarette smoking, and/or alcohol consumption, if these factors exist.

Physicians should instruct their patients to read the Patient Information before starting therapy with ACTONEL 35 mg and to re-read it each time the prescription is renewed.

Patients should be reminded to give all of their health care providers an accurate medication history. Instruct patients to tell all of their health care providers that they are taking ACTONEL. Patients should be instructed that any time they have a medical problem they think may be from ACTONEL, they should talk to their doctor.

CALCIUM

Calcium should be used as an adjunct to osteoporosis therapies.

The patient should be informed to take the calcium tablets with food to facilitate calcium absorption.

Drug Interactions:

ACTONEL

No specific drug-drug interaction studies were performed. Risedronate is not metabolized and does not induce or inhibit hepatic microsomal drug-metabolizing enzymes (Cytochrome P450).

Calcium Supplements/Antacids:

Co-administration of ACTONEL and calcium, antacids, or oral medications containing divalent cations will interfere with the absorption of ACTONEL.

Hormone Replacement Therapy:

One study of about 500 early postmenopausal women has been conducted to date in which treatment with ACTONEL (5 mg/day) plus estrogen replacement therapy was compared to estrogen replacement therapy alone. Exposure to study drugs was approximately 12 to 18 months and the primary endpoint was change in BMD. If considered appropriate, ACTONEL may be used concomitantly with hormone replacement therapy.

Aspirin/Nonsteroidal Anti-Inflammatory Drugs (NSAIDs):

Of over 5700 patients enrolled in the ACTONEL Phase 3 osteoporosis studies, aspirin use was reported by 31% of patients, 24% of whom were regular users (3 or more days per week). Forty-eight percent of patients reported NSAID use, 21% of whom were regular users. Among regular aspirin or NSAID users, the incidence of upper gastrointestinal adverse experiences in ACTONEL-treated patients (24.5%) was similar to that in placebo-treated patients (24.8%).

H2 Blockers and Proton Pump Inhibitors (PPIs):

Of over 5700 patients enrolled in the ACTONEL Phase 3 osteoporosis studies, 21% used H2 blockers and/or PPIs. Among these patients, the incidence of upper gastrointestinal adverse experiences in the ACTONEL-treated patients was similar to that in placebo-treated patients.

CALCIUM

Bisphosphonates:

Oral bisphosphonates (such as risedronate, alendronate, etidronate, ibandronate): Decreased absorption of the bisphosphonate may occur when the bisphosphonate and calcium are taken together.

Thyroid hormones:

Levothyroxine: Concomitant intake of levothyroxine and calcium carbonate was found to reduce levothyroxine absorption and increase serum thyrotropin levels.

Fluoroquinolones:

Fluoroquinolones (such as ciprofloxacin, moxifloxacin, and ofloxacin): Concomitant administration of a fluoroquinolone and calcium carbonate may decrease the absorption of the fluoroquinolone.

Systemic glucocorticoids:

Calcium absorption is reduced when calcium carbonate is taken concomitantly with systemic glucocorticoids.

Tetracyclines:

Tetracyclines (such as doxycycline, minocycline, tetracycline): Concomitant administration of a tetracycline and calcium carbonate may decrease the absorption of the tetracycline.

Thiazide diuretics:

Reduced urinary excretion of calcium has been reported during concomitant use of calcium carbonate and thiazide diuretics.

Vitamin D:

Vitamin D and vitamin D analogues (such as calcitriol, doxercalciferol, and paricalcitol): Absorption of calcium may be increased when calcium carbonate is given concomitantly with vitamin D analogues.

Iron:

Calcium may interfere with the absorption of iron. Patients being treated for iron deficiency should take iron and calcium at different times of the day.

Drug/Laboratory Test Interactions:

ACTONEL

Bisphosphonates are known to interfere with the use of bone-imaging agents. Specific studies with ACTONEL have not been performed.

Carcinogenesis, Mutagenesis, Impairment of Fertility:

Carcinogenesis:

In a 104-week carcinogenicity study, rats were administered daily oral doses of risedronate up to 24 mg/kg/day (approximately 50 times the systemic exposure following a 35 mg/week human dose based on surface area, mg/m2). There were no significant drug-induced tumor findings in male or female rats. The high dose male group of 24 mg/kg/day was terminated early in the study (Week 93) due to excessive toxicity, and data from this group were not included in the statistical evaluation of the study results. In an 80-week carcinogenicity study, mice were administered daily oral doses up to 32 mg/kg/day (approximately 30 times the systemic exposure following a 35 mg/week human dose based on surface area, mg/m2). There were no significant drug-induced tumor findings in male or female mice.

Mutagenesis:

Risedronate did not exhibit genetic toxicity in the following assays: In vitro bacterial mutagenesis in Salmonella and E. coli (Ames assay), mammalian cell mutagenesis in CHO/HGPRT assay, unscheduled DNA synthesis in rat hepatocytes and an assessment of chromosomal aberrations in vivo in rat bone marrow.

Impairment of Fertility:

In female rats, ovulation was inhibited at an oral dose of risedronate of 16 mg/kg/day (approximately 30 times the systemic exposure following a 35 mg/week human dose based on surface area, mg/m2). Decreased implantation was noted in female rats treated with doses ≥7 mg/kg/day (14 times the systemic exposure following a 35 mg/week human dose based on surface area, mg/m2). In male rats, testicular and epididymal atrophy and inflammation were noted at 40 mg/kg/day (80 times the systemic exposure following a 35 mg/week human dose based on surface area, mg/m2). Testicular atrophy was also noted in male rats after 13 weeks of treatment at oral doses of 16 mg/kg/day (approximately 30 times the systemic exposure following a 35 mg/week human dose based on surface area, mg/m2). There was moderate-to-severe spermatid maturation block after 13 weeks in male dogs at an oral dose of 8 mg/kg/day (approximately 50 times the systemic exposure following a 35 mg/week human dose based on surface area, mg/m2).

Pregnancy:

Pregnancy Category C: Survival of neonates was decreased in rats treated during gestation with oral doses of risedronate ≥16 mg/kg/day (approximately 30 times the systemic exposure following a 35 mg/week human dose based on surface area, mg/m2). Body weight was decreased in neonates from dams treated with 80 mg/kg (approximately 160 times the 35 mg/week human dose based on surface area, mg/m2). In rats treated during gestation, the number of fetuses exhibiting incomplete ossification of sternebrae or skull was statistically significantly increased at 7.1 mg/kg/day (approximately 14 times the 35 mg/week human dose based on surface area, mg/m2). Both incomplete ossification and unossified sternebrae were increased in rats treated with oral doses ≥16 mg/kg/day (approximately 30 times the 35 mg/week human dose based on surface area, mg/m2). A low incidence of cleft palate was observed in fetuses from female rats treated with oral doses ≥3.2 mg/kg/day (approximately 20 times the 35 mg/week human dose based on surface area, mg/m2). The relevance of this finding to human use of ACTONEL is unclear. No significant fetal ossification effects were seen in rabbits treated with oral doses up to 10 mg/kg/day during gestation (40 times the 35 mg/week human dose based on surface area, mg/m2). However, in rabbits treated with 10 mg/kg/day, 1 of 14 litters were aborted and 1 of 14 litters were delivered prematurely.

Similar to other bisphosphonates, treatment during mating and gestation with doses as low as 3.2 mg/kg/day (approximately 20 times the 35 mg/week human dose based on surface area, mg/m2) has resulted in periparturient hypocalcemia and mortality in pregnant rats allowed to deliver.

Bisphosphonates are incorporated into the bone matrix, from which they are gradually released over periods of weeks to years. The amount of bisphosphonate incorporation into adult bone, and hence, the amount available for release back into the systemic circulation, is directly related to the dose and duration of bisphosphonate use. There are no data on fetal risk in humans. However, there is a theoretical risk of fetal harm, predominantly skeletal, if a woman becomes pregnant after completing a course of bisphosphonate therapy. The impact of variables such as time between cessation of bisphosphonate therapy to conception, the particular bisphosphonate used, and the route of administration (intravenous versus oral) on this risk has not been studied.

There are no adequate and well-controlled studies of ACTONEL in pregnant women. ACTONEL should be used during pregnancy only if the potential benefit justifies the potential risk to the mother and fetus.

Nursing Women:

Risedronate was detected in feeding pups exposed to lactating rats for a 24-hour period post-dosing, indicating a small degree of lacteal transfer. It is not known whether risedronate is excreted in human milk. Because many drugs are excreted in human milk and because of the potential for serious adverse reactions in nursing infants from bisphosphonates, a decision should be made whether to discontinue nursing or to discontinue the drug, taking into account the importance of the drug to the mother.

Pediatric Use:

ACTONEL

Safety and effectiveness in pediatric patients have not been established.

Geriatric Use:

ACTONEL

Of the patients receiving ACTONEL in postmenopausal osteoporosis studies (see CLINICAL STUDIES), 47% were between 65 and 75 years of age, and 17% were over 75. No overall differences in efficacy or safety were observed between these patients and younger patients but greater sensitivity of some older individuals cannot be ruled out.

CALCIUM

There are no published data that specifically compare the efficacy and safety between postmenopausal women above and below the age of 65 years.

Use in Men:

ACTONEL

The safety and effectiveness in men for the treatment of primary osteoporosis have not been established.

ADVERSE REACTIONS

ACTONEL

Osteoporosis:

ACTONEL has been studied in over 5700 patients enrolled in the Phase 3 glucocorticoid-induced osteoporosis clinical trials and in postmenopausal osteoporosis trials of up to 3-years duration. The overall adverse event profile of ACTONEL 5 mg in these studies was similar to that of placebo. Most adverse events were either mild or moderate and did not lead to discontinuation from the study. The incidence of serious adverse events in the placebo group was 24.9% and in the ACTONEL 5 mg group was 26.3%. The percentage of patients who withdrew from the study due to adverse events was 14.4% and 13.5% for the placebo and ACTONEL 5 mg groups, respectively. Table 4 lists adverse events from the Phase 3 osteoporosis trials reported in ≥2% of patients and in more ACTONEL-treated patients than placebo-treated patients. Adverse events are shown without attribution of causality.

Table 4   Adverse Events Occurring at a Frequency ≥2% and in More ACTONEL-Treated Patients than Placebo-Treated Patients:  Combined Phase 3 Osteoporosis Trials
Body System Placebo
%
(N = 1914)
ACTONEL 5 mg
%
(N = 1916)
Body as a Whole
    Infection 29.7 29.9
    Back Pain 23.6 26.1
    Pain 13.1 13.6
    Abdominal Pain 9.4 11.6
    Neck Pain 4.5 5.3
    Asthenia 4.3 5.1
    Chest Pain 4.9 5.0
    Neoplasm 3.0 3.3
    Hernia 2.5 2.9
Cardiovascular
    Hypertension 9.0 10.0
    Cardiovascular Disorder 1.7 2.5
    Angina Pectoris 2.4 2.5
Digestive
    Nausea 10.7 10.9
    Diarrhea 9.6 10.6
    Flatulence 4.2 4.6
    Gastritis 2.3 2.5
    Gastrointestinal Disorder 2.1 2.3
    Rectal Disorder 1.9 2.2
    Tooth Disorder 2.0 2.1
Hemic and Lymphatic
    Ecchymosis 4.0 4.3
    Anemia 1.9 2.4
Musculoskeletal
    Arthralgia 21.1 23.7
    Joint Disorder 5.4 6.8
    Myalgia 6.3 6.6
    Bone Pain 4.3 4.6
    Bone Disorder 3.2 4.0
    Leg Cramps 2.6 3.5
    Bursitis 2.9 3.0
    Tendon Disorder 2.5 3.0
Nervous
    Depression 6.2 6.8
    Dizziness 5.4 6.4
    Insomnia 4.5 4.7
    Anxiety 3.0 4.3
    Neuralgia 3.5 3.8
    Vertigo 3.2 3.3
    Hypertonia 2.1 2.2
    Paresthesia 1.8 2.1
Respiratory
    Pharyngitis 5.0 5.8
    Rhinitis 5.0 5.7
    Dyspnea 3.2 3.8
    Pneumonia 2.6 3.1
Skin and Appendages
    Rash 7.2 7.7
    Pruritus 2.2 3.0
    Skin Carcinoma 1.8 2.0
Special Senses
    Cataract 5.4 5.9
    Conjunctivitis 2.8 3.1
    Otitis Media 2.4 2.5
Urogenital
    Urinary Tract Infection 9.7 10.9
    Cystitis 3.5 4.1

Duodenitis and glossitis have been reported uncommonly (0.1% to 1%). There have been rare reports (<0.1%) of abnormal liver function tests.

Laboratory Test Findings:

Asymptomatic and small decreases were observed in serum calcium and phosphorus levels. Overall, mean decreases of 0.8% in serum calcium and of 2.7% in phosphorus were observed at 6 months in patients receiving ACTONEL. Throughout the Phase 3 studies, serum calcium levels below 8 mg/dL were observed in 18 patients, 9 (0.5%) in each treatment arm (ACTONEL and placebo). Serum phosphorus levels below 2 mg/dL were observed in 14 patients, 11 (0.6%) treated with ACTONEL and 3 (0.2%) treated with placebo.

Endoscopic Findings:

ACTONEL clinical studies enrolled over 5700 patients, many with pre-existing gastrointestinal disease and concomitant use of NSAIDs or aspirin. Investigators were encouraged to perform endoscopies in any patients with moderate-to-severe gastrointestinal complaints, while maintaining the blind. These endoscopies were ultimately performed on equal numbers of patients between the treated and placebo groups [75 (14.5%) placebo; 75 (11.9%) ACTONEL]. Across treatment groups, the percentage of patients with normal esophageal, gastric, and duodenal mucosa on endoscopy was similar (20% placebo; 21% ACTONEL). The number of patients who withdrew from the studies due to the event prompting endoscopy was similar across treatment groups. Positive findings on endoscopy were also generally comparable across treatment groups. There was a higher number of reports of mild duodenitis in the ACTONEL group, however there were more duodenal ulcers in the placebo group. Clinically important findings (perforations, ulcers, or bleeding) among this symptomatic population were similar between groups (51% placebo; 39% ACTONEL).

Once-a-week Dosing:

In a 1-year, double-blind, multicenter study comparing ACTONEL 5 mg daily and ACTONEL 35 mg once a week in postmenopausal women, the overall safety and tolerability profiles of the 2 oral dosing regimens were similar. Table 5 lists the adverse events in ≥2% of patients from this trial. Events are shown without attribution of causality.

Table 5   Adverse Events Occurring in ≥ 2% of Patients of Either Treatment Group in the Daily vs. Weekly Osteoporosis Treatment Study in Postmenopausal Women
Body System 5 mg Daily
ACTONEL
%
(N = 480)
35 mg Weekly
ACTONEL
%
(N = 485)
Body as a Whole
    Infection 19.0 20.6
    Accidental Injury 10.6 10.7
    Pain 7.7 9.9
    Back Pain 9.2 8.7
    Flu Syndrome 7.1 8.5
    Abdominal Pain 7.3 7.6
    Headache 7.3 7.2
    Overdose 6.9 6.8
    Asthenia 3.5 5.4
    Chest Pain 2.3 2.7
    Allergic Reaction 1.9 2.5
    Neoplasm 0.8 2.1
    Neck Pain 2.7 1.2
Cardiovascular System
    Hypertension 5.8 4.9
    Syncope 0.6 2.1
    Vasodilatation 2.3 1.4
Digestive System
    Constipation 12.5 12.2
    Dyspepsia 6.9 7.6
    Nausea 8.5 6.2
    Diarrhea 6.3 4.9
    Gastroenteritis 3.8 3.5
    Flatulence 3.3 3.1
    Colitis 0.8 2.5
    Gastrointestinal Disorder 1.9 2.5
    Vomiting 1.9 2.5
    Dry Mouth 2.5 1.4
Metabolic and Nutritional Disorders
    Peripheral Edema 4.2 1.6
Musculoskeletal System
    Arthralgia 11.5 14.2
    Traumatic Bone Fracture 5.0 6.4
    Myalgia 4.6 6.2
    Arthritis 4.8 4.1
    Bursitis 1.3 2.5
    Bone Pain 2.9 1.4
Nervous System
    Dizziness 5.8 4.9
    Anxiety 0.6 2.7
    Depression 2.3 2.3
    Vertigo 2.1 1.6
Respiratory System
    Bronchitis 2.3 4.9
    Sinusitis 4.6 4.5
    Pharyngitis 4.6 2.9
    Cough Increased 3.1 2.5
    Pneumonia 0.8 2.5
    Rhinitis 2.3 2.1
Skin and Appendages
    Rash 3.1 4.1
    Pruritus 1.9 2.3
Special Senses
    Cataract 2.9 1.9
Urogenital System
    Urinary Tract Infection 2.9 5.2
Osteoporosis Prevention:

There were no deaths in a 1-year, double-blind, placebo-controlled study of ACTONEL 35 mg once a week for prevention of bone loss in 278 postmenopausal women without osteoporosis. More treated subjects on risedronate experienced arthralgia (risedronate 13.9%; placebo 7.8%), myalgia (risedronate 5.1%; placebo 2.1%), and nausea (risedronate 7.3%; placebo 4.3%) than subjects on placebo.

Post-marketing Experience:

Very rare hypersensitivity and skin reactions have been reported, including angioedema, generalized rash and bullous skin reactions, some severe.

Musculoskeletal: bone, joint, or muscle pain, rarely described as severe or incapacitating (see PRECAUTIONS, Musculoskeletal Pain).

Very rare reactions of eye inflammation including iritis and uveitis have been reported.

Osteonecrosis of the jaw has been reported very rarely (see PRECAUTIONS, General).

CALCIUM

Calcium carbonate may cause gastrointestinal adverse effects such as constipation, flatulence, nausea, abdominal pain, and bloating. Administration of calcium may increase the risk of kidney stones, particularly in patients with a history of this condition (see PRECAUTIONS).

OVERDOSAGE

ACTONEL

Decreases in serum calcium and phosphorus following substantial overdose may be expected in some patients. Signs and symptoms of hypocalcemia may also occur in some of these patients. Milk or antacids containing calcium should be given to bind ACTONEL and reduce absorption of the drug.

In cases of substantial overdose, gastric lavage may be considered to remove unabsorbed drug. Standard procedures that are effective for treating hypocalcemia, including the administration of calcium intravenously, would be expected to restore physiologic amounts of ionized calcium and to relieve signs and symptoms of hypocalcemia.

Lethality after single oral doses was seen in female rats at 903 mg/kg and male rats at 1703 mg/kg. The minimum lethal dose in mice and rabbits was 4000 mg/kg and 1000 mg/kg. These values represent >1000 times the 35 mg/week human dose based on surface area (mg/m2).

CALCIUM

Because of its limited intestinal absorption, overdosage with calcium carbonate is unlikely. However, prolonged use of very high doses can lead to hypercalcemia. Clinical manifestations of hypercalcemia may include anorexia, thirst, nausea, vomiting, constipation, abdominal pain, muscle weakness, fatigue, mental disturbances, polydipsia, polyuria, bone pain, nephrocalcinosis, renal calculi and in severe cases, cardiac arrhythmias.

Treatment: Calcium should be discontinued. Other therapies that may be contributing to the condition, such as thiazide diuretics, lithium, vitamin A, vitamin D and cardiac glycosides should also be discontinued. Gastric emptying of any residual calcium should be considered. Rehydration, and, according to severity, isolated or combined treatment with loop diuretics, bisphosphonates, calcitonin and corticosteroids should also be considered. Serum electrolytes, renal function and vital signs must be monitored.

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, 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 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.

HOW SUPPLIED

ACTONEL with CALCIUM 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

NDC 0149-0475-01

Store at 20°-25°C (68°-77°F); excursions permitted between 15°-30°C (59°-86°F) [See USP Controlled Room Temperature].

Actonel sold under U.S. patent No. 5,583,122; 5,935,602; 5,994,329; 6,015,801; 6,047,829; 6,096,342; 6,165,513; 6,225,294; 6,410,520; 6,432,932; 6,465,443; and 6,562,974.

Actonel mfg. by: Procter & Gamble Pharmaceuticals, Inc.
Cincinnati, OH 45202, or
Norwich Pharmaceuticals, Inc.
North Norwich, NY 13814

Calcium mfg. by: Norwich Pharmaceuticals, Inc.
North Norwich, NY 13814

Dist. by: Procter & Gamble Pharmaceuticals, Inc., TM Owner
Cincinnati, OH 45202

Marketed with: sanofi-aventis U.S. LLC
Bridgewater, NJ 08807

JANUARY 2008

Patient Information

ACTONEL® (AK-toh-nel) with CALCIUM

ACTONEL (risedronate sodium tablets) 35 mg with CALCIUM (calcium carbonate tablets, USP) 1250 mg (equals 500 mg elemental calcium) for Postmenopausal Osteoporosis

Read this information carefully before you start to use your medicine. Read the information you get every time you get more medicine. There may be new information. This information does not take the place of talking with your health care provider about your medical condition or your treatment. If you have any questions or are not sure about something, ask your health care provider or pharmacist.

What is the most important information I should know about ACTONEL with CALCIUM?

ACTONEL may cause problems in your stomach and esophagus (the tube that connects the mouth and the stomach), such as trouble swallowing (dysphagia), heartburn (esophagitis), and ulcers. You might feel pain in your bones, joints, or muscles (See "What are the Possible Side Effects of ACTONEL with CALCIUM?").

You must follow the instructions exactly for ACTONEL with CALCIUM to work and to lower the chance of serious side effects. (See "How should I take ACTONEL with CALCIUM").

What is ACTONEL with CALCIUM?

  • ACTONEL with CALCIUM is a prescription medicine used to prevent and treat osteoporosis in postmenopausal women (See "What is Osteoporosis?").

ACTONEL may reverse bone loss by stopping more loss of bone and increasing bone strength in most people who take it, even though they won't be able to see or feel a difference. ACTONEL helps lower the risk of breaking bones (fractures). Your health care provider may measure the thickness (density) of your bones or do other tests to check your progress.

Calcium is the main mineral that makes up your bones and teeth. Your body cannot make calcium. Calcium must come from the food you eat or from a calcium tablet. If your bones do not get enough calcium over time, they can become weak and break (fracture) easier.

See the end of this leaflet for information about osteoporosis.

Who should not take ACTONEL with CALCIUM?

Do not take ACTONEL if you:

  • have low blood calcium (hypocalcemia)
  • cannot sit or stand up for 30 minutes
  • have kidneys that work poorly
  • have an allergy to ACTONEL. The active ingredient in ACTONEL is risedronate sodium. (See the end of this leaflet for a list of all the ingredients in ACTONEL).

Do not take Calcium if you:

  • have high blood calcium (hypercalcemia)
  • have an allergy to any ingredient in this product. (See the end of this leaflet for a list of all the ingredients.)

Tell your doctor before using ACTONEL if:

  • you are pregnant or may become pregnant. We do not know if ACTONEL can harm your unborn child.
  • you are breast-feeding or plan to breast-feed. We do not know if ACTONEL can pass through your milk and if it can harm your baby.
  • you have kidney problems. ACTONEL may not be right for you.

Tell your doctor about all the medicines you take, including prescription and non-prescription medicines, vitamins and herbal supplements. ACTONEL and Calcium can interact with other medicines. Keep a list of all the medicines you take. Show it to all your healthcare providers, including your dentist and pharmacist, each time you get a new medicine.

Tell your doctor before using Calcium if:

  • you have a history of kidney stones.
  • you are already taking calcium supplements.

How should I take ACTONEL with CALCIUM?

Actonel Tablets:

  • Choose 1 day of the week that you will remember and that best fits your schedule to take your ACTONEL 35- mg. Every week, take 1 ACTONEL 35- mg (orange) tablet in the morning on your chosen day.
  • Take ACTONEL first thing in the morning before you eat or drink anything except plain water.
  • Take ACTONEL while you are sitting up or standing.
  • Take ACTONEL with 6 to 8 ounces (about 1 cup) of plain water. Do not take it with any other drink besides plain water. Do not take it with coffee, tea, juice, milk or other dairy drinks.
  • Swallow ACTONEL whole. Do not chew the tablet or keep it in your mouth to melt or dissolve.
  • After taking ACTONEL you must wait at least 30 minutes BEFORE:
    • lying down. You may sit, stand, or do normal activities like read the newspaper or take a walk.
    • eating or drinking anything except plain water.
    • taking vitamins, calcium, or antacids. Take vitamins, calcium, and antacids at a different time of the day from when you take ACTONEL.

Calcium Tablets:

  • Take one Calcium (blue) tablet daily with food for the following 6 days of the week.
  • When you have completed the week's regimen (one ACTONEL tablet on the first day followed by one Calcium tablet on each of the remaining 6 days), begin taking the next week's supply (refer back to the beginning of this section entitled "How Should I Take ACTONEL with CALCIUM").

Keep taking ACTONEL with CALCIUM for as long as your health care provider tells you.

For ACTONEL to treat your postmenopausal osteoporosis or keep you from getting postmenopausal osteoporosis, you have to take it exactly as prescribed.

Your health care provider may tell you to take more calcium as well as vitamin D and to exercise. If you take more calcium tablets, take each calcium tablet at separate times of the day with food. All calcium tablets should be taken at a different time of day than your ACTONEL tablet.

What should I do if I miss a dose of my ACTONEL?

  • If you miss a dose of your ACTONEL 35- mg (orange) tablet in the morning, do not take it later in the day. Take only 1 ACTONEL 35- mg tablet the next morning and return to your usual schedule. Take your Calcium (blue) tablet with food later in the same day that the missed ACTONEL tablet is taken. Do not take your ACTONEL and Calcium tablet at the same time.

What should I do if I miss a dose of Calcium?

  • If you miss a dose of a Calcium (blue) tablet and remember later in the day, you may take it with food.
  • If you miss a dose of a Calcium tablet the entire day, and you remember the next day, you may take two tablets on that day at separate times with food.
  • Do not take more than two Calcium tablets on the same day, unless recommended by your health care provider.

What should I avoid while taking ACTONEL with CALCIUM?

  • Do not eat or drink anything except water before you take ACTONEL and for at least 30 minutes after you take it.
  • Do not lie down for at least 30 minutes after you take ACTONEL.
  • Foods and some vitamin supplements and medicines can stop your body from absorbing (using) ACTONEL. Therefore, do not take anything other than plain water at or near the time you take ACTONEL. (See "How should I take ACTONEL?").

What are the possible side effects of ACTONEL with CALCIUM?

Stop taking ACTONEL and tell your health care provider right away if:

  • swallowing is difficult or painful
  • you have chest pain
  • you have very bad heartburn or it doesn't get better

ACTONEL may cause:

  • pain or trouble swallowing (dysphagia)
  • heartburn (esophagitis)
  • ulcers in your stomach and esophagus (the tube that connects the mouth and the stomach)
  • pain in bones, joints, or muscles, sometimes severe. Pain may start as soon as one day or up to several months after starting ACTONEL.

The most common side effects with ACTONEL include back pain, joint pain, upset stomach, abdominal (stomach area) pain, constipation, diarrhea, gas, and headache. Tell your health care provider if you have pain or discomfort in your stomach or esophagus. Rarely, severe skin reactions may occur. Patients may get allergic reactions such as rash, hives, or in rare cases, swelling that can be of the face, lips, tongue, or throat, which may cause trouble breathing or swallowing.

In rare cases, patients taking Actonel may get eye inflammation, usually with pain, redness and sensitivity to light.

Rarely, patients had had jaw problems associated with delayed healing and infection, often following tooth extraction.

These are not all the possible side effects of ACTONEL. You can ask your health care provider or pharmacist about other side effects. Any time you have a medical problem you think may be from ACTONEL, talk to your doctor.

Calcium may cause:

  • constipation
  • gas
  • nausea
  • abdominal pain
  • bloating
  • an increased chance of kidney stones

What is osteoporosis?

Osteoporosis is a disease that causes bones to become thinner. Thin bones can break easily. Most people think of their bones as being solid like a rock. Actually, bone is living tissue, just like other parts of the body—your heart, brain, or skin, for example. Bone just happens to be a harder type of tissue. Bone is always changing. Your body keeps your bones strong and healthy by replacing old bone with new bone.

Osteoporosis causes the body to remove more bone than it replaces. This means that bones get weaker. Weak bones are more likely to break. Osteoporosis is a bone disease that is quite common, especially in older women. However, young people and men can develop osteoporosis, too. Osteoporosis can be prevented, and with proper therapy it can be treated.

How can osteoporosis affect me?

  • You may not have any pain or other symptoms when osteoporosis begins.
  • You are more likely to break (fracture) a bone especially if you fall because osteoporosis makes your bones weaker. You are most likely to break a bone in your back (spine), wrist, or hip.
  • You may "shrink" (get shorter).
  • You may get a "hump" (curve) in your back.
  • You may have bad back pain that makes you stop some activities.

Who is at risk for osteoporosis?

Many things put women at risk for osteoporosis. The following women have a higher chance of getting Osteoporosis:

Women who

  • are going through or who are past menopause ("the change")
  • are white (Caucasian) or Asian
  • are thin
  • have a family member with osteoporosis
  • do not get enough calcium or vitamin D
  • do not exercise
  • smoke
  • drink alcohol often
  • take bone thinning medicines (like prednisone or other corticosteroids) for a long time

General information about ACTONEL with CALCIUM:

Medicines are sometimes prescribed for conditions that are not mentioned in patient information leaflets. Do not use ACTONEL with CALCIUM for a condition for which it was not prescribed. Do not give ACTONEL with CALCIUM to other people, even if they have the same symptoms you have. It may harm them.

What if I have other questions about ACTONEL with CALCIUM?

This leaflet summarizes the most important information about ACTONEL with CALCIUM for osteoporosis. If you have more questions about ACTONEL with CALCIUM, ask your health care provider or pharmacist. They can give you information written for health care professionals. For more information, call 1-877-ACTONEL (toll-free) or visit our web site at www.actonel.com.

What are the ingredients of ACTONEL?

ACTONEL (active ingredient): risedronate sodium.

ACTONEL (inactive ingredients): crospovidone, ferric oxide red, ferric oxide yellow, hydroxypropyl cellulose, hydroxypropyl methylcellulose, lactose monohydrate, magnesium stearate, microcrystalline cellulose, polyethylene glycol, silicon dioxide, and titanium dioxide.

What are the ingredients of Calcium?

Calcium carbonate (1250 mg, equals 500 mg elemental calcium), pregelatinized starch, sodium starch glycolate, polyethylene glycol 3350, hypromellose, magnesium stearate, opaspray light blue, FD&C blue #2, polysorbate 80.

ACTONEL® with CALCIUM is marketed by:
Procter & Gamble Pharmaceuticals, Inc.
Cincinnati, OH 45202
and
sanofi-aventis U.S. LLC

Bridgewater, NJ 08807

August 2006

© 2006 Procter & Gamble Pharmaceuticals, Inc.

PRINCIPAL DISPLAY PANEL - 28 Tablet Carton

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