Numerous dietary supplements are marketed for weight loss. Reliable evidence of

efficacy for these agents is limited and safety data are lacking. Clinical data do not

support the use of these agents and S.B. should be advised not to use dietary

supplement for weight loss.

CASE 36-1, QUESTION 9: S.B.’s health insurance changed and she was no longer able to continue orlistat

and she slowly regained the lost weight. Two years after discontinuing orlistat, SB has regained 7 kg. Her

current weight is 85 kg and her BMI is 30.1 kg/m

2

. She is frustrated that she has regained weight despite

compliance with comprehensive lifestyle interventions. She asks whether her results are usual and inquires

about additional options for weight loss.

S.B.’s regain after discontinuing orlistat is typical. Trials with a crossover design

have shown that the weight loss achieved with anti-obesity agents is unlikely to be

sustained after discontinuation.

6 Weight regain is to be expected after discontinuing

anti-obesity agents because the underlying pathology of obesity is not changed.

Medical Devices for Obesity Treatment

A device called the vBloc Maestro Rechargeable System has been recently approved

by the FDA as a treatment option for patients with extreme obesity (BMI ≥40 or ≥35

kg/m2 with comorbid conditions) who have failed at least one supervised weight

management program within the past 5 years.

124 The device is surgically implanted

into the abdomen where it emits intermittent electrical pulses to block signaling by

the vagus nerve.

124,125

In a recent randomized, double-blind, sham-controlled clinical

trial, the vBloc system produced weight loss of 9.2% of initial body weight,

compared to weight loss of 6.0% of initial body weight with the sham technology.

126

The most common adverse events were heartburn, dyspepsia, and abdominal pain.

126

S.B.’s current BMI is 30.1 kg/m2 which is below the threshold for use of vBloc;

therefore, she is not a candidate for a medical device at this time. In order to sustain

weight loss, long-term treatment must continue.

CASE 36-1, QUESTION 10: S.B. returns to her physician 3 years later. She has gained an additional 16 kg

and her BMI is now 35.4 kg/m

2

. She reports inability to maintain her weight with diet and exercise therapy after

completion of the behavioral modification program in which she was participating. Laboratory tests provide the

following results:

Blood pressure, 154/92 mm Hg

Fasting blood glucose, 162 mg/dL

TG, 354 mg/dL

Total cholesterol, 227 mg/dL

HDL, 35 mg/dL

LDL, 182 mg/dL

S.B. requests a referral to a bariatric clinic for evaluation for surgical intervention for weight loss. Is S.B. a

candidate for bariatric surgery? How could a bariatric surgical procedure affect medication administration in

S.B. postoperatively?

Surgery

Surgery may be an option for individuals with extreme obesity (BMI ≥40 or ≥35

kg/m2 with comorbid conditions) who have not responded to lifestyle changes with or

without adjunctive pharmacotherapy.

7,127 For severely obese patients (>100% more

than normal weight), the most effective treatment is a surgical procedure to reduce

the size of the stomach. Bariatric surgical procedures either reduce the absorptive

surface of the GI tract resulting in malabsorption, or reduce the stomach volume so

that the person feels full after a smaller meal. Procedures include gastric banding,

vertical banded gastroplasty, Roux-en-Y gastric bypass, and biliopancreatic

diversion; all have demonstrated efficacy, although the degree of weight loss and

complications may differ.

128 Gastric bypass has been shown to produce a greater

weight loss compared with gastroplasty procedures.

129

In addition, laparoscopic (vs.

open surgical) approaches may be preferred for reducing postoperative

complications and hospital stay.

128

The mortality rate from bariatric surgery is estimated to be 0.3% to 1.9% and

literature has shown that centers that perform surgeries at high volume have better

outcomes.

67 Some of the complications of bariatric surgery include nausea, stomach

ulceration, stenosis, anemia, and cholelithiasis. Postsurgical precautions include

careful evaluation of meal sizes and timing along with meal content, especially

immediately after surgery. Patients should be aware that they will not be able to

resume their normal eating habits, and they should be properly educated on lifestyle

modifications for maintenance of weight loss. In addition, medications and adequate

intake of necessary nutrients are important considerations after surgery. Medications

such as nonsteroidal anti-inflammatory drugs, salicylates, and bisphosphonates may

cause ulcerations, and medications that are delayed release or extended release may

not be absorbed owing to changes in gastric size.

130 Medications may need to be

administered using liquid formulation and other dosage routes. Transdermal

formulations need to be carefully dosed to account for changes in body surface area

postsurgically.

130

Although S.B. is a candidate for bariatric surgery based on her BMI of 35.4 kg/m2

and her comorbid conditions (hypertension and sleep apnea), she may also consider

alternative pharmacotherapeutic options. S.B.’s fasting blood glucose indicates that

she may have type 2 diabetes. Liraglutide is an option that will lower her blood

glucose as well as result in clinically significant weight reduction.

KEY REFERENCES AND WEBSITES

A full list of references for this chapter can be found at

http://thepoint.lww.com/AT11e. Below are the key references and websites for this

chapter, with the corresponding reference number in this chapter found in parentheses

after the reference.

Key References

Apovian CM et al. Pharmacological management of obesity: an endocrine society clinical practice guideline. J Clin

Endocrinol Metab. 2015;100(2):342–362. (6)

Domecq JP et al. Drugs commonly associated with weight change: a systematic review and meta-analysis. J Clin

Endocrinol Metab. 2015;100(2):363–370. (57)

Garvey WT et al. Two-year sustained weight loss and metabolic benefits with controlled-release

phentermine/topiramate in obese and overweight adults (SEQUEL): a randomized, placebo-controlled, phase 3

extension study. Am J Clin Nutr. 2012;95(2):297–308. (93)

Jensen MD et al. 2013 AHA/ACC/TOS guideline for the management of overweight and obesity in adults: a report

of the American college of cardiology/American heart association task force on practice guidelines and the

obesity society. J Am Coll Cardiol. 2014;63(25_PA):2985–3023. (7)

Pi-Sunyer X et al. A randomized, controlled trial of 3.0 mg of liraglutide in weight management. N Engl J Med.

2015;373(1):11–22. (115)

Rucker D et al. Long term pharmacotherapy for obesity and overweight: updated meta-analysis. BMJ.

2007;335(7631):1194–1199. (77)

p. 766

p. 767

Smith SR et al. Multicenter, placebo-controlled trial of lorcaserin for weight management. N Engl J Med.

2010;363(3):245–256. (98)

Snow V et al. Pharmacologic and surgical management of obesity in primary care: a clinical practice guideline

from the American College of Physicians. Ann Intern Med. 2005;142(7):525–531. (66)

Torgerson JS et al. XENical in the prevention of diabetes in obese subjects (XENDOS) study:A randomized study

of orlistat as an adjunct to lifestyle changes for the prevention of type 2 diabetes in obese patients. Diabetes

Care. 2004;27(1):155–161. (78)

Yanovski SZ, Yanovski JA. Long-term drug treatment for obesity: a systematic and clinical review. JAMA.

2014;311(1):74–86. (67)

Key Websites

Obesity Action Coalition. http://www.obesityaction.org/.

CDC. http://www.cdc.gov/obesity/.

NIH. http://www.nhlbi.nih.gov/health/educational/wecan/healthy-weight-basics/obesity.htm.

COMPLETE REFERENCES CHAPTER 36 OBESITY

WHO obesity and overweight. http://www.who.int/mediacentre/factsheets/fs311/en/. Accessed July 24, 2015.

Mechanick J et al. American association of clinical endocrinologists’ position statement on obesity and obesity

medicine. Endocr Pract. 2012;18:642–648.

Ogden CL et al. Prevalence of childhood and adult obesity in the United States, 2011–2012. JAMA.

2014;311(8):806–814.

Ng M et al. Global, regional, and national prevalence of overweight and obesity in children and adults during 1980–

2013: a systematic analysis for the global burden of disease study 2013. Lancet. 2014;384(9945):766–781.

Hammond RA, Levine R. The economic impact of obesity in the United States. Diabetes Metab Syndr Obes.

2010;3:285–295.

Apovian CM et al. Pharmacological management of obesity: An endocrine society clinical practice guideline. J Clin

Endocrinol Metab. 2015;100(2):342–362.

Jensen MD et al. 2013 AHA/ACC/TOS guideline for the management of overweight and obesity in adults: a report

of the american college of cardiology/American heart association task force on practice guidelines and the

obesity society. J Am Coll Cardiol. 2014;63(25_PA):2985–3023.

Bhaskaran K et al. Body-mass index and risk of 22 specific cancers: a population-based cohort study of 5 24

million UK adults. Lancet. 2014;384(9945):755–765.

Deurenberg P et al. Asians are different from Caucasians and from each other in their body mass index/body fat

per cent relationship. Obes Rev. 2002;3(3):141–146.

Janssen I et al. Body mass index, waist circumference, and health risk: evidence in support of current national

institutes of health guidelines. Arch Intern Med. 2002;162(18):2074–2079.

Canoy D et al. Body fat distribution and risk of coronary heart disease in men and women in the European

prospective investigation into cancer and nutrition in Norfolk cohort: a population-based prospective study.

Circulation. 2007;116(25):2933–2943.

Ko GT, Tang JS. Waist circumference and BMI cut-off based on 10-year cardiovascular risk: evidence for

“Central Pre-Obesity”. Obesity. 2007;15(11):2832–2839.

Cerhan JR et al. A pooled analysis of waist circumference and mortality in 650,000 adults. Mayo Clin Proc.

2014;89(3):335–345.

Guo SS et al. Predicting overweight and obesity in adulthood from body mass index values in childhood and

adolescence. Am J Clin Nutr. 2002;76(3):653–658.

Reilly J, Kelly J. Long-term impact of overweight and obesity in childhood and adolescence on morbidity and

premature mortality in adulthood:systematic review. Int J Obes. 2011;35(7):891–898.

Wright SM, Aronne LJ. Causes of obesity. Abdom Imaging. 2012;37(5):730–732.

Taheri S. The link between short sleep duration and obesity: we should recommend more sleep to prevent obesity.

Arch Dis Child. 2006;91(11):881–884.

Cappuccio FP et al. Meta-analysis of short sleep duration and obesity in children and adults. Sleep.

2008;31(5):619–626.

Reilly JJ et al. Early life risk factors for obesity in childhood: Cohort study. BMJ. 2005;330(7504):1357.

Moraes W et al. Association between body mass index and sleep duration assessed by objective methods in a

representative sample of the adult population. Sleep Med. 2013;14(4):312–318.

Taheri S et al. Short sleep duration is associated with reduced leptin, elevated ghrelin, and increased body mass

index. PLoS Med. 2004;1(3):210.

Ajslev T et al. Childhood overweight after establishment of the gut microbiota: the role of delivery mode, prepregnancy weight and early administration of antibiotics. Int J Obes (Lond). 2011;35(4):522–529.

Bailey LC et al. Association of antibiotics in infancy with early childhood obesity. JAMA Pediatr.

2014;168(11):1063–1069.

Yang W et al. Genetic epidemiology of obesity. Epidemiol Rev. 2007;29:49–61.

Silventoinen K et al. The genetic and environmental influences on childhood obesity: a systematic review of twin

and adoption studies. Int J Obes. 2010;34(1):29–40.

Wardle J et al. Evidence for a strong genetic influence on childhood adiposity despite the force of the obesogenic

environment. Am J Clin Nutr. 2008;87(2):398–404.

Bouchard C. Childhood obesity: are genetic differences involved? Am J Clin Nutr. 2009;89(5):1494S–1501S.

Segal N et al. Genetic and environmental contributions to body mass index: comparative analysis of monozygotic

twins, dizygotic twins and same-age unrelated siblings. Int J Obes (Lond). 2009;33(1):37–41.

Ortega-Alonso A et al. Genetic influences on adult body mass index followed over 29 years and their effects on

late-life mobility: a study of twin sisters. J Epidemiol Community Health. 2009;63(8):651–658.

Guo Y et al. Gene-centric meta-analyses of 108 912 individuals confirm known body mass index loci and reveal

three novelsignals. Hum Mol Genet. 2013;22(1):184–201.

Schleinitz D et al. The genetics of fat distribution. Diabetologia. 2014;57(7):1276–1286.

Licinio J et al. The hypothalamic-pituitary-adrenal axis in anorexia nervosa. Psychiatry Res. 1996;62(1):75–83.

Gurevich-Panigrahi T et al. Obesity: pathophysiology and clinical management. Curr Med Chem. 2009;16(4):506–

521.

Valassi E et al. Neuroendocrine control of food intake. Nutr Metab Cardiovasc Dis. 2008;18(2):158–168.

Jimerson DC, Wolfe BE. Neuropeptides in eating disorders. CNS Spectr. 2004;9(07):516–522.

BlundellJE, Halford JC. Serotonin and appetite regulation. CNS Drugs. 1998;9(6):473–495.

Gorwood P et al. Genetics and anorexia nervosa: a review of candidate genes. Psychiatr Genet. 1998;8(1):1–12.

Sinha MK, Caro JF. Clinical aspects of leptin. Vitam Horm. 1998;54:1–30.

Sawa M, Harada H. Recent developments in the design of orally bioavailable β3

-adrenergic receptor agonists.

Curr Med Chem. 2006;13(1):25–37.

Ferron F et al. Serum leptin concentrations in patients with anorexia nervosa, bulimia nervosa and non-specific

eating disorders correlate with the body mass index but are independent of the respective disease. Clin

Endocrinol (Oxf). 1997;46(3):289–293.

Houseknecht KL et al. The biology of leptin: a review. J Anim Sci. 1998;76(5):1405–1420.

Campfield LA et al. Strategies and potential molecular targets for obesity treatment. Science.

1998;280(5368):1383–1387.

Considine RV et al. Serum immunoreactive-leptin concentrations in normal-weight and obese humans. N Engl J

Med. 1996;334(5):292–295.

Flier JS, Maratos-Flier E. Obesity and the hypothalamus: novel peptides for new pathways. Cell. 1998;92(4):437–

440.

Cooper JA et al. Serum leptin levels in obese males during over-and underfeeding. Obesity. 2009;17(12):2149–

2154.

Crujeiras AB et al. Weight regain after a diet-induced loss is predicted by higher baseline leptin and lower ghrelin

plasma levels. J Clin Endocrinol Metab. 2010;95(11):5037–5044.

Fuentes T et al. Leptin receptor 170 kDa (OB-R170) protein expression is reduced in obese human skeletal

muscle: a potential mechanism of leptin resistance. Exp Physiol. 2010;95(1):160–171.

Heymsfield SB et al. Recombinant leptin for weight loss in obese and lean adults: a randomized, controlled, doseescalation trial. JAMA. 1999;282(16):1568–1575.

Suzuki K et al. Obesity and appetite control. Exp Diabetes Res. 2012;2012:824305.

Zhang Y et al. Obesity: pathophysiology and intervention. Nutrients. 2014;6(11):5153–5183.

Gantz I et al. Efficacy and safety of intranasal peptide YY3–36 for weight reduction in obese adults. J Clin

Endocrinol Metab. 2007;92(5):1754–1757.

Sloth B et al. Effect of subcutaneous injections of PYY1-36 and PYY3-36 on appetite, ad libitum energy intake,

and plasma free fatty acid concentration in obese males. Am J Physiol Endocrinol Metab. 2007;293(2):E604–

E609.

Smith SR et al. Sustained weight loss following 12-month pramlintide treatment as an adjunct to lifestyle

intervention in obesity. Diabetes Care. 2008;31(9):1816–1823.

Reinehr T. Obesity and thyroid function. Mol Cell Endocrinol. 2010;316(2):165–171.

Verma A et al. Hypothyroidism and obesity cause or effect? Saudi Med J. 2008;29(8):1135–1138.

Krotkiewski M. Thyroid hormones in the pathogenesis and treatment of obesity. Eur J Pharmacol.

2002;440(2):85–98.

Domecq JP et al. Drugs commonly associated with weight change: a systematic review and meta-analysis. J Clin

Endocrinol Metab. 2015;100(2):363–370.

Fava M et al. Fluoxetine versus sertraline and paroxetine in major depressive disorder: changes in weight with

long-term treatment. J Clin Psychiatry. 2000;61(11):863–867.

Sumithran P et al. Long-term persistence of hormonal adaptations to weight loss. N Engl J Med.

2011;365(17):1597–1604.

Malnick SD, Knobler H. The medical complications of obesity. QJM. 2006;99(9):565–579.

Hidalgo LG. Dermatological complications of obesity. Am J Clin Dermatol. 2002;3(7):497–506.

Sacks FM et al. Comparison of weight-loss diets with different compositions of fat, protein, and carbohydrates. N

EnglJ Med. 2009;360(9):859–873.

Church TS et al. Effects of different doses of physical activity on cardiorespiratory fitness among sedentary,

overweight or obese postmenopausal women with elevated blood pressure: a randomized controlled trial.

JAMA. 2007;297(19):2081–2091.

Dansinger ML et al. Comparison of the atkins, ornish, weight watchers, and zone diets for weight loss and heart

disease risk reduction: a randomized trial. JAMA. 2005;293(1):43–53.

Yager J, Powers P, eds. Clinical Manual of Eating Disorders. Arlington, VA: American Psychiatric Publishing;

2007.

Snow V et al. Pharmacologic and surgical management of obesity in primary care: a clinical practice guideline

from the American College of Physicians. Ann Intern Med. 2005;142(7):525–531.

Yanovski SZ, Yanovski JA. Long-term drug treatment for obesity: a systematic and clinical review. JAMA.

2014;311(1):74–86.

Zhang Z, Wang M. Obesity, a health burden of a global nature. Acta Pharmacol Sin. 2012;33(2):145–147.

Kang J et al. Randomized controlled trial to investigate the effects of a newly developed formulation of

phentermine diffuse-controlled release for obesity. Diabetes Obes Metab. 2010;12(10):876–882.

Cosentino G et al. Phentermine and topiramate for the management of obesity: a review. Drug Des Devel Ther.

2013;7:267.

Bang W et al. Pulmonary hypertension associated with use of phentermine. Yonsei Med J. 2010;51(6):971–973.

Xenical PI, ed. Xenical (orlistat) capsules for oral use [prescribing information]. South San Francisco, CA:

Genentech USA; 2013.

Williams G. Orlistat over the counter. BMJ. 2007;335(7631):1163–1164.

James WP et al. A one-year trial to assess the value of orlistat in the management of obesity. Int J Obes Relat

Metab Disord. 1997;21(Suppl 3):S24–S30.

Guerciolini R. Mode of action of orlistat. Int J Obes Relat Metab Disord. 1997;21(Suppl 3):S12–S23.

Bray GA, Ryan DH. Update on obesity pharmacotherapy. Ann N Y Acad Sci. 2014;1311(1):1–13.

Rucker D et al. Long term pharmacotherapy for obesity and overweight: updated meta-analysis. BMJ.

2007;335(7631):1194–1199.

Torgerson JS et al. XENical in the prevention of diabetes in obese subjects (XENDOS) study: a randomized study

of orlistat as an adjunct to lifestyle changes for the prevention of type 2 diabetes in obese patients. Diabetes

Care. 2004;27(1):155–161.

Yancy WS et al. A randomized trial of a low-carbohydrate diet vs orlistat plus a low-fat diet for weight loss. Arch

Intern Med. 2010;170(2):136–145.

de Castro JJ et al. A randomized double-blind study comparing the efficacy and safety of orlistat versus placebo

in obese patients with mild to moderate hypercholesterolemia. Rev Port Cardiol. 2009;28(12):1361–1374.

Padwal RS, Majumdar SR. Drug treatments for obesity: orlistat, sibutramine, and rimonabant. Lancet.

2007;369(9555):71–77.

Weir MA et al. Orlistat and acute kidney injury: an analysis of 953 patients. Arch Intern Med. 2011;171(7):702–

710.

Morris M et al. An integrated analysis of liver safety data from orlistat clinical trials. Obes Facts. 2012;5(4):485–

494.

Kaplan LM. Pharmacologic therapies for obesity. Gastroenterol Clin North Am. 2010;39(1):69–79.

Bigham S et al. Reduced absorption of lipophilic anti-epileptic medications when used concomitantly with the antiobesity drug orlistat. Epilepsia. 2006;47(12):2207.

Qsymia PI, ed. Qsymia (phentermine and topiramate extended-release) capsules [prescribing information].

Mountain View, CA: Vivus; 2014.

Jordan J et al. Cardiovascular effects of phentermine and topiramate: a new drug combination for the treatment

of obesity. J Hypertens. 2014;32(6):1178–1188.

Werneke U et al. Options for pharmacological management of obesity in patients treated with atypical

antipsychotics. Int Clin Psychopharmacol. 2002;17(4):145–160.

Eliasson B et al. Weight loss and metabolic effects of topiramate in overweight and obese type 2 diabetic patients:

Randomized double-blind placebo-controlled trial. Int J Obes (Lond). 2007;31(7):1140–1147.

Gadde KM et al. Effects of low-dose, controlled-release, phentermine plus topiramate combination on weight and

associated comorbidities in overweight and obese adults (CONQUER): a randomised, placebo-controlled, phase

3 trial. Lancet. 2011;377(9774):1341–1352.

Allison DB et al. Controlled-Release phentermine/topiramate in severely obese adults: a randomized controlled

trial (EQUIP). Obesity. 2012;20(2):330–342.

Garvey WT et al. Two-year sustained weight loss and metabolic benefits with controlled-release

phentermine/topiramate in obese and overweight adults (SEQUEL): a randomized, placebo-controlled, phase 3

extension study. Am J Clin Nutr. 2012;95(2):297–308.

Risk evaluation and mitigation strategy (REMS) qsymia® (phentermine and topiramate extended-release)

capsules CIV. http://www.qsymiarems.com/. Accessed July 25, 2015, 2015.

Belviq PI, ed. Belviq (lorcaserin hydrochloride) [prescribing information]. Woodcliff Lake, NJ: Eisai; 2014.

Thomsen WJ et al. Lorcaserin, a novel selective human 5-hydroxytryptamine2C agonist: In vitro and in vivo

pharmacological characterization. J Pharmacol Exp Ther. 2008;325(2):577–587.

Heisler LK et al. Serotonin reciprocally regulates melanocortin neurons to modulate food intake. Neuron.

100.

101.

102.

103.

104.

105.

106.

107.

108.

109.

110.

111.

112.

113.

114.

115.

116.

117.

118.

119.

120.

121.

122.

123.

2006;51(2):239–249.

Smith SR et al. Multicenter, placebo-controlled trial of lorcaserin for weight management. N Engl J Med.

2010;363(3):245–256.

Fidler MC et al. A one-year randomized trial of lorcaserin for weight loss in obese and overweight adults: the

BLOSSOM trial. J Clin Endocrinol Metab. 2011;96(10):3067–3077.

O’Neil PM et al. Randomized placebo-controlled clinical trial of lorcaserin for weight loss in type 2 diabetes

mellitus: the BLOOM-DM study. Obesity. 2012;20(7):1426–1436.

Smith SR et al. Lorcaserin (APD356), a selective 5-HT2C agonist, reduces body weight in obese men and

women. Obesity. 2009;17(3):494–503.

Weissman NJ et al. Echocardiographic assessment of cardiac valvular regurgitation with lorcaserin from

analysis of 3 phase 3 clinical trials. Circ Cardiovasc Imaging. 2013;6(4):560–567.

Contrave PI, ed. Contrave (naltrexone HCl and bupropion HCl) extended releast tablets [prescribing

information]. Deerfield, IL: Takeda Pharmaceuticals America; 2014.

Comments

Search This Blog

Archive

Show more

Popular posts from this blog

TRIPASS XR تري باس

CELEPHI 200 MG, Gélule

ZENOXIA 15 MG, Comprimé

VOXCIB 200 MG, Gélule

Kana Brax Laberax

فومي كايند

بعض الادويه نجد رموز عليها مثل IR ، MR, XR, CR, SR , DS ماذا تعني هذه الرموز

NIFLURIL 700 MG, Suppositoire adulte

Antifongiques مضادات الفطريات

Popular posts from this blog

علاقة البيبي بالفراولة بالالفا فيتو بروتين

التغيرات الخمس التي تحدث للجسم عند المشي

إحصائيات سنة 2020 | تعداد سكَان دول إفريقيا تنازليا :

ما هو الليمونير للأسنان ؟

ACUPAN 20 MG, Solution injectable

CELEPHI 200 MG, Gélule

الام الظهر

VOXCIB 200 MG, Gélule

ميبستان

Popular posts from this blog

TRIPASS XR تري باس

CELEPHI 200 MG, Gélule

Popular posts from this blog

TRIPASS XR تري باس

CELEPHI 200 MG, Gélule

ZENOXIA 15 MG, Comprimé

VOXCIB 200 MG, Gélule

Kana Brax Laberax

فومي كايند

بعض الادويه نجد رموز عليها مثل IR ، MR, XR, CR, SR , DS ماذا تعني هذه الرموز

NIFLURIL 700 MG, Suppositoire adulte

Antifongiques مضادات الفطريات

Popular posts from this blog

Kana Brax Laberax

TRIPASS XR تري باس

PARANTAL 100 MG, Suppositoire بارانتال 100 مجم تحاميل

الكبد الدهني Fatty Liver

الم اسفل الظهر (الحاد) الذي يظهر بشكل مفاجئ bal-agrisi

SEDALGIC 37.5 MG / 325 MG, Comprimé pelliculé [P] سيدالجيك 37.5 مجم / 325 مجم ، قرص مغلف [P]

نمـو الدمـاغ والتطـور العقـلي لـدى الطفـل

CELEPHI 200 MG, Gélule

أخطر أنواع المخدرات فى العالم و الشرق الاوسط

Archive

Show more