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Buy Fosamax. Fosamax is a bisphosphonate used to prevent and treat osteoporosis.

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Uses

Fosamax is used to treat and prevent osteoporosis and to treat Paget's disease. Fosamax is also used to treat osteoporosis that is caused by treatment with a corticosteroid.

In osteoporosis it works by slowing down the process of old bone being removed, which allows the bone-forming cells time to rebuild normal bone. FOSAMAX not only helps prevent the loss of bone but actually helps to rebuild bone and makes bone less likely to fracture. Thus, FOSAMAX reverses the progression of osteoporosis. FOSAMAX starts working on the bone cells immediately, but measurable effects on bone mass may not be seen for several months or more.

FOSAMAX belongs to a group of non-hormonal medicines called bisphosphonates.

 

Directions

Take Fosamax only as prescribed

 

Possible Side Effects

Stop taking Fosamax and seek emergency medical attention or contact your doctor immediately if you experience any of the following serious side effects. An allergic reaction (difficulty breathing; closing of your throat; swelling of your lips, tongue, or face; or hives);

Tell your doctor if you are taking any other medicines, including medicines that you buy without a prescription from your pharmacy, supermarket or health food shop. Some medicines may affect the way other medicines work.

Some medicines are likely to interfere with the absorption of FOSAMAX if taken at the same time. These include:

antacids, such as Aludrox™, Aludrox Plus™, Amphojel™, Andrews Effervescent™, Eno™ powder, Gavisgon™, Mylanta™, Quickeze™, Roter™, Titralac™, Titralac-Sil™, Tums™, Ural™. calcium supplements.vitamins.

Therefore, take FOSAMAX at least 30 minutes before taking any of these or other medicines to make sure there is no problem with absorption. Check with your doctor or pharmacist if you are not sure whether you are taking an antacid.

You can take aspirin while you are being treated with FOSAMAX. However, both aspirin and FOSAMAX may increase the chance of stomach upsets.

Your doctor or pharmacist has more information on medicines to be careful with or avoid while taking FOSAMAX.

 

Overdose

The symptoms of an Fosamax overdose are unknown, but the following symptoms might be expected: nausea, heartburn, pain in your abdomen, other stomach-related symptoms, muscle cramps, uncontrollable facial grimacing, seizures, irritability, and abnormal behavior.

 

Storage

Keep your tablets in the blister pack until it is time to take them. If you take the tablets out of the blister pack they may not keep well.

Keep FOSAMAX in a cool dry place where the temperature stays below 30°C. Do not store it or any other medicine in the bathroom or near a sink.

Do not leave it in the car or on window sills. Heat and dampness can destroy some medicines.

Keep it where children cannot reach it. A locked cupboard at least one-and-a-half metres above the ground is a good place to store medicines.

 

 

 

 

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Evista

For the treatment and prevention of osteoporosis in postmenopausal women.
Evista (Raloxifene) is a selective estrogen receptor modulator (SERM) that belongs to the benzothiophene class of compounds. The SERM profile of raloxifene includes estrogen agonist effects on bone and lipid metabolism but not in uterine or breast tissues.
In women of childbearing potential. Evista (raloxifene) therapy during pregnancy may be associated with an increased risk of congenital defects in the fetus.
evista (Raloxifene) is contraindicated in women with active or past history of venous thromboembolic events, including deep vein thrombosis, pulmonary embolism and retinal vein thrombosis.
Evista (Raloxifene) is contraindicated in women known to be hypersensitive to raloxifene or other constituents of the tablets.

In clinical trials, raloxifene-treated women had an increased risk of venous thromboembolism (deep vein thrombosis and pulmonary embolism). Other venous thromboembolic events could also occur. A less serious event, superficial thrombophlebitis, also has been reported more frequently with raloxifene. The greatest risk for deep vein thrombosis and pulmonary embolism occurs during the first 4 months of treatment, and the magnitude of risk is similar to that associated with use of hormone replacement therapy. Evista (Raloxifene) should be discontinued at least 72 hours prior to and during prolonged immobilization (e.g., postsurgical recovery, prolonged bed rest) and raloxifene therapy should be resumed only after the patient is fully ambulatory. The risk-benefit balance should be considered in women at risk of thromboembolic disease for other reasons.
There is no indication for premenopausal use of Evista (Raloxifene). Safety of Evista (Raloxifene) in premenopausal women has not been established and its use is not recommended.
Evista (Raloxifene) was studied, as a single dose, in Child-Pugh Class A patients with cirrhosis and serum total bilirubin ranging from 0.6 to 2 mg/dL (10.3 to 34.2 µmol/L). Plasma raloxifene concentrations were approximately 2.5 times higher than in controls and correlated with total bilirubin concentrations. Safety and efficacy have not been evaluated further in patients with hepatic insufficiency.
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