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Why should you buy Tramaden instead of a prescription pain medication like Tramadol?

Side Effects Of Tramadol:
This medication may cause dizziness, weakness, incoordination, nausea or vomiting, stomach upset, constipation, headache, drowsiness, anxiety, irritability, dry mouth, or increased sweating. If any of these effects persist or worsen, inform your doctor. Notify your doctor if you develop any of these serious effects while taking this medication: chest pain, rapid heart rate, skin rash or itching, mental confusion, disorientation, seizures, tingling of the hands or feet, trouble breathing. In the unlikely event you have an allergic reaction to this drug, seek immediate medical attention. Symptoms of an allergic reaction include: rash, itching, swelling, dizziness, breathing trouble. If you notice other effects not listed above, contact your doctor or pharmacist.

Side Effects Of Tramaden:
This medication will stop your pain and aches. It won't cause you drowsiness or your ability to think. You won't get depended on it either.


                          

                                                               

 

Tramaden ™, our pharmaceutical grade non-buy natural pain medicationprescription pain relief formula designed to produce effects similar to popular prescription drugs without the dangerous side effects!!

It gives you true relief! Buy tramaden for back pain, neck pain or any everyday pain that you want gone!

 
 

 

Tramaden™  is designed to produce effects similar to the most popular pain  medications  prescription .

Product Quanity Regular Price Sale PriceImage Order
Tramaden 1 month   60 caps $59.00 $53.00 Buy Tramaden now
Tramaden 3 months 180 caps $149.00 $129.00 Buy Tramaden now

With the FDA Public Health Advisory statement that clinical trials showed drugs such as Vioxx and Celebrex might be associated with an increased risk of serious health problems, people have been wondering where to turn for safe and effective pain relief.

Directions for Use: Take 2 capsules daily.

 

 

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TRAMADEN RESEARCH: A brief overview of some key ingredients: CELADRIN ® - Celadrin® is a medically and clinically proven all-natural pain management compound comprised of novel, targeted and proprietary cetylated fatty acid esters and select other active synergists, that has been shown to reduce inflammation and pain with no side effects. Celadrin has been proven to provide cumulative (continuous and restorative) benefit. In a double blind clinical trial, oral Celadrin showed significant benefit beyond the arthritic medication the subjects were taking - with cumulative improvement shown throughout the study The anti-inflammatory actions of Celadrin have been demonstrated by a double-blind, placebo controlled trial that showed Celadrin, when taken orally at recommended intake levels, decreased pain scores and increased walking distance compared to the group receiving placebo. The authors theorize that Celadrin may work by down-regulating the effect of certain precursors of the body's inflammatory response.1 In a double blind, matched pair study conducted at the University of Connecticut, 100% of the osteoarthritic subjects on Celadrin showed significant improvement in just 30 minutes and cumulative benefits throughout the remaining 30 days of the study. Patients were assessed for range of motion, pain levels, timed up and go, timed stair climbing and muscular endurance tests. Significance was demonstrated in every test. Along with other studies and scientific presentations, Celadrin has been published on two occasions in the internationally acclaimed Journal of Rheumatology. Among other benefits: *Celadrin has been shown to be very safe & efficacious as evidenced by gold standard, double-blind, placebo-controlled clinical & scientific studies. *Celadrin is FDA compliant and non prescriptive. *Celadrin is clinically proven effective in providing speedy relief to aching, painful joints and muscles. *Over 100 million Celadrin pills have been distributed to date with NO REPORTED ADVERSE SIDE EFFECTS! Loss of cell membrane integrity from both internal and external stressors precipitates a number of aging processes - including uncontrolled inflammation. Inflammation can occur as a result of aging, dietary habits, free radicals, stress or other factors which adversely affect cell membranes and in turn could lead to one or more forms of arthritis (bursitis and tendonitis included), periodontal disease, wrinkles, cardiovascular disease (CVD), rapid aging and other related maladies. Celadrin not only halts the cascade of inflammation but rapidly begins restoring the body on a cumulative basis. Flexibility is restored, pain is eliminated and appearance of wrinkles is reversed. Celadrin accomplishes these features by enhancing the lipid structure of the cell membrane and converting it to a super membrane enabling the cells to rapidly repair and regenerate. This unique enhancement of the cell membrane leads to the multitude of restorative, healing and age reversing attributes of Celadrin - including arthritis and inflammatory conditions. References: 1 .Hesslink R Jr., et al. Cetylated fatty acids improve knee function in patients with osteoarthritis. J Rheumatology 2002;8:1708-1712. 2. Kraemer WJ, et al. Effect of a cetylated fatty acid topical cream on functional mobility and quality of life of patients with osteoarthritis. J Rheumatology 2004;4:767-74. 3. Rovati LC. Clinical research in osteoarthritis: design and results of short-term and long-term trials with disease modifying drugs. Int J Tissue React 1992;14:243-51. MSM (Methylsulfonylmethane) is a naturally occurring substance used by the body to build connective tissue and amino acids. Research shows that MSM is a safe, non-toxic (its toxicity profile is similar to that of water) method of controlling the pain of arthritis. One study at Oregon Health Sciences University found that animals given MSM showed no degeneration of cartilage associated with rheumatoid arthritis. Studies in human volunteers with arthritis showed a 60 percent improvement in pain after taking MSM for four weeks. After six weeks, the improvement rate rose to 82 percent. References ; 1. Hucker HB and others. Studies on the absorption, excretion and metabolism of dimethylsulfoxide in man. Journal of Pharmacology and Experimental Therapeutics 155:309-317, 1967. 2. Jacob S, Lawrence RM, Zucker M. The Miracle of MSM: The Natural Solution for Pain. New York: Penguin-Putnam, 1999. 3. Herschler RJ. Dietary and pharmaceutical uses of methylsulfonylmethane and compositions comprising it. U.S. Patent 4,514,421. April 30, 1985. 4. Herschler RJ. Methylsulfonylmethane in dietary products. U.S. Patent 4,616,039. Oct 7, 1986. 5. Lignisul MSM (Methylsulfonylmethane) A Double Blind Study Of Its Use In Degenerative Arthritis by Ronald M. Lawrence, M.D., Ph.D.Assistant Clinical Professor U.C.L.A. School of Medicine Los Angeles, California 4/10/01 HYALURONIC ACID (Hyaluronan): A component of connective tissue whose function is to cushion and lubricate, it has the physiological functions of absorbing water into intercellular space, making jelly matrix, protecting the cell structure and defending against external threats and bacterial infections. Hyaluronic acid is used for relief of fibromylagia and tissue reconstruction. Hyaluronan occurs throughout the body in abundant amounts in many of the places people with hereditary connective tissue disorders have problems such as joints, heart valves and eyes. Hyaluronic acid abnormalities are a common thread in connective tissue disorders. Interestingly, they are also common biochemical anomalies in most of the individual features of connective tissue disorders such as mitral valve prolapse, TMJ, osteoarthritis, and keratoconus References: 1. Rheumataology (Oxford) 1999 Jul;38 (7):602-7 Hyaluronic acid in the treatment of osteoarthritis of the knee; Huskisson EC, Donnelly S. Department of Rheumatology, St Bartholomew's Hospital, West Smithfield, London, UK 2. George E. Intra-articular hyaluronan treatment for osteoarthritis. Ann Rheum Dis 1998;57:637-40. 3. Wobig M, Bach G, Beks P, Dickhut A, Runzheimer J, Schwieger G, et al. The role of elastoviscosity in the efficacy of viscosupplementation for osteoarthritis of the knee: a comparison of hylan G-F 20 and a lower-molecular-weight hyaluronan. Clin Ther 1999;21:1549-62. 4. Cohen MD. Hyaluronic acid treatment (viscosupplementation) for OA of the knee. Bull Rheum Dis 1998;47:4-7. 5. Balazs EA, Denlinger JL. Viscosupplementation: a new concept in the treatment of osteoarthritis. J Rheumatol 1993;20(suppl 39):3-9. 6. Peyron JG, Balazs EA. Preliminary clinical assessment of Na-hyaluronate injection into human arthritic joints. Pathol Biol [Paris] 1974;22:731-6. 7. Weiss C, Balazs EA, St. Onge R, Denlinger JL. Clinical studies of the intraarticular injection of HealonR (sodium hyaluronate) in the treatment of osteoarthritis of human knees. Osteoarthritis symposium. Palm Aire, Fla., October 20-22, 1980. Semin Arthritis Rheum. 1981;11(suppl 1):143-4. 8. Peyron JG. Intraarticular hyaluronan injections in the treatment of osteoarthritis: state-of-the-art review. J Rheumatol 1993;39(suppl):10-5. 9. Dahlberg L, Lohmander LS, Ryd L. Intraarticular injections of hyaluronan in patients with cartilage abnormalities and knee pain. A one-year double-blind, placebo-controlled study. Arthritis Rheum 1994;37:521-8. 10. Henderson EB, Smith EC, Pegley F, Blake DR. Intra-articular injections of 750 kD hyaluronan in the treatment of osteoarthritis: a randomised single centre double-blind placebo-controlled trial of 91 patients demonstrating lack of efficacy. Ann Rheum Dis 1994;53:529-34. 11. Lohmander LS, Dalen N, Englund G, Hamalainen M, Jensen EM, Karlsson K, et al. Intra-articular hyaluronan injections in the treatment of osteoarthritis of the knee: a randomised, double blind, placebo controlled multicentre trial. Hyaluronan Mulicentre Trial Group. Ann Rheum Dis 1996;55:424-31. 12. Dougados M, Nguyen M, Listrat V, Amor B. High molecular weight sodium hyaluronate (hyalectin) in osteoarthritis of the knee: a 1 year placebo-controlled trial. Osteoarthritis Cart 1993;1:97-103. 13. Puhl W, Bernau A, Greiling H, Kopcke W, Pforringer W, Steck KJ, et al. Intraarticular sodium hyaluronate in osteoarthritis of the knee: a multicentre double- blind study. Osteoarthritis Cart 1993;1:233-41. 14. Listrat V, Ayral X, Paternello F, Bonvarlet JP, Simonnet J, Amor B, et al. Arthroscopic evaluation of potential structure modifying activity of hyaluronan (Hyalgan) in osteoarthritis of the knee. Osteoarthritis Cart 1997;5:153-60. 15. Altman RD, Moskowitz R. Intraarticular sodium hyaluronate (Hyalgan) in the treatment of patients with osteoarthritis of the knee: a randomized clinical trial. J Rheumatol 1998;25:2203-12 [Published erratum appears in J Rheumatol 1999;26:1216]. 16. Adams ME. An analysis of clinical studies of the use of crosslinked hyaluronan, hylan, in the treatment of osteoarthritis. J Rheumatol (suppl) 1993;39:16-8. 17. Wobig M, Dickhut A, Maier R, Vetter G. Viscosupplementation with hylan G-F 20: a 26-week controlled trial of efficacy and safety in the osteoarthritic knee. Clin Ther 1998;20:410-23. 18. Adams ME, Atkinson MH, Lussier AJ, Schulz JI, Siminovitch KA, Wade JP, et al. The role of viscosupplementation with hylan G-F 20 (Synvisc) in the treatment of osteoarthritis of the knee: a Canadian multicenter trial comparing hylan G-F 20 alone, hylan G-F 20 with non-steroidal anti-inflammatory drugs (NSAIDs) and NSAIDs alone. Osteoarthritis Cart 1995;3:213-25. 19. Lussier A, Cividino AA, McFarlane CA, Olszynski WP, Potashner WJ, De Medicis R. Viscosupplementation with hylan for the treatment of osteoarthritis: findings from clinical practice in Canada. J Rheumatol 1996;23:1579-85. Maheu E. Hyaluronan in knee osteoarthritis: a review of the clinical trials with hyalgan. Eur J Rheumatol Inflamm 1995;15:17-24. BOSWELLIA SERRATA: Used for relief of bursitis, osteoarthritis and rheumatoid arthritis. Studies have shown that the boswellic acids have an inflammatory action, similar to conventional non-steroidal anti-inflammatory drugs (NSAIDS) but unlike NSAIDS, long term use of boswellia does not lead to irritation or ulceration of the stomach. Research done in India and Germany has recently confirmed Boswellias therapeutic efficacy; it has shown advantages over other nonsteroidal anti-inflammatory agents (NSAIDs) and has suggested a mechanism by which it acts. Much of the research has been conducted at the Regional Research Laboratory in Jammu, India. Here, investigators have subjected Boswellia extract, also referred to as alcohol extract of sallaki guggal (AESG), to many testing procedures. Acute, subacute, and chronic toxicity tests in three mammalian species, including a species of primate, revealed no significant changes in blood or tissue biochemistry. Under test conditions in the laboratory the LD-50 (a dose at which 50% of the test organisms die) of rats was greater than 2 grams per Kg, apparently making Boswellia extract safer than ibuprofen, which has an LD-50 of 1.6 grams per Kg. Boswellia and Arthritis: Researchers have found that the anti-inflammatory herb Boswellia serrata can relieve the pain of osteoarthritis of the knee. In a randomized, double-blind, placebo-controlled study, researchers gave Boswellia serrata Extract (BSE) to 30 patients with osteoarthritis of the knee. The study authors used a crossover design, which means that 15 patients received the Boswellia serrata for eight weeks while the other 15 received a placebo. At the end of the eight weeks, the subjects switched treatments so that the 15 who had been on the placebo began taking the Boswellia serrata and the 15 who had taken the herb began taking the placebo. All patients receiving the Boswellia serrata treatment reported decrease in knee pain, increased ability to bend the knee and increased walking distance. The frequency of swelling in the knee joint also was decreased. The improvement was statistically significant. The researchers recommended Boswellia serrata for the treatment of osteoarthritis of the knee and suggested that it might be equally effective in treating other types of arthritis. Reference: Kimmatkar N, Thawani V, Hingorani L, Khiyani R. Efficacy and tolerability of Boswellia serrata extract in treatment of osteoarthritis of knee--a randomized double blind placebo controlled trial. Phytomedicine. 2003 Jan;10(1):3-7. Additional Resources: Immunonodulatory activity of boswellic acids of Boswellia serrata - Indian J Exp Biol. 2003 Dietary support with Boswellia resin canine inflammatory joint and spinal disease - Schweiz Arch Tierheilkd. 2004 Boswellic acids as the active principle in treatment of chronic inflammatory diseases - Wien Med Wochenschr. 2002 BROMELAIN: The name of a group of proteolytic enzymes that are found in the pineapple plant (Ananas comosus). Bromelain is particularly useful for reducing muscle and tissue inflammation. It is a natural blood thinner and anti-inflammatory that works by breaking down fibrin, a blood-clotting protein that can impede good circulation and prevent tissues from draining properly. It also blocks the production of compounds that can cause swelling and pain. Bromelain is used to alleviate back pain and chronic joint pain associated with arthritis, to treat sprains, strains, and muscle aches, to reduce swelling and pain of gout, relieve carpal tunnel syndrome, and lessen the swelling and accelerate the healing of cuts and scrapes and insect bites and stings. 1. Heinicke RM, Van der Wal M, Yokoyama MM. Effect of bromelain on human platelet aggrega tion. Experientia 1972;28:844-845. 2. Morita AH, Uchida DA, Taussig SJ. Chromato graphic fractionation and characterization of the active platelet aggregation inhibitory factor from bromelain. Arch Inter Phar Ther 1979;239:340-350. 3. Livio M, Bertoni MP, De Gaetano G, et al. Effect of bromelain on fibrinogen level, prothrombin complex factors and platelet aggregation in the rat - A preliminary report. Drugs Expt Clin Res 1978;4:49-53. 4. De-Giuli M, Pirotta F. Bromelain: interaction with some protease inhibitors and rabbit specific antiserum. Drugs Exp Clin Res 1978;4:21-23. 5. Inoue K, Motonaga A, Dainaka J, et al. Effect of etodolac on prostaglandin E2 biosynthesis, active oxygen generation and bradykinin formation. Prostaglandins Leukot Essent Fatty Acids 1994;51:457-462. 6. Uhlig G, Seifert J. The effect of proteolytic enzymes (traumanase) on posttraumatic edema. Fortschr Med 1981;99:554-556. 7. Vellini M, Desideri D, Milanese A, et al. Possible involvement of eicosanoids in the pharmacological action of bromelain. Arzneimittelforschung 1986;36:110-112. 8. Yonehara N, Shibutani T, Inoki R. Contribution of substance P to heat-induced edema in rat paw. J Pharmacol Exp Ther 1987;242:1071-1076. 9. Kumakura S, Yamashita M, Tsurufuji S. Effect of bromelain on kaolin-induced inflammation in rats. Eur J Pharmacol 1988;150:295-301. 10. Uchida Y, Katori M. Independent consumption of high and low molecular weight kininogens in vivo. Adv Exp Med Biol 1986;198:113-118. 11. Taussig SJ, Batkin S. Bromelain, the enzyme complex of pineapple (Ananas comosus) and its clinical application. An update. J Ethnopharmacol 1988;22:191-203. HOLY BASIL: This herb is a natural substance that does essentially the same things as Vioxx and Celebrex. It inhibits the production of the Cox-2 enzyme primarily responsible for inflammation pain and it does so WITHOUT any side effects. References: Indian J Exp Biol. 1990 Nov;28(11):1008-11