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Fosamax (Alendronate)

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Fosamax is used to prevent and treat certain types of bone loss (osteoporosis) in adults. Osteoporosis causes bones to become thinner and break more easily. This medication works by slowing bone loss. Fosamax belongs to a class of drugs called bisphosphonates.

Other names for this medication:
Alant, Alendix, Alendronate, Alenost, Bifosa, Denfos, Osteofos, Ostogee, Poronil, Ralenost, Restofos, Zophost

Similar Products:
Phenergan, Requip, Differin, Neoral, Lioresal, Motrin, Xeloda

Also known as: Alendronate


Generic Fosamax is a drug which helps to fight with postmenopausal osteoporosis, steroid-induced osteoporosis, Pagets disease of bone. Generic Fosamax is a medicine which belongs to the group of medicines called bisphosphonates. Fosamax is also known as Alendronic acid, Alendronate sodium, Ostofos. Generic Fosamax works by preventing bone breakdown and increasing bone density (thickness). Generic name of Generic Fosamax is Alendronate. Brand name of Generic Fosamax is Fosamax.


Take Fosamax Plus D exactly as it was prescribed for you. Follow all directions on your prescription label. Do not take this medicine in larger or smaller amounts or for longer than recommended.

Fosamax Plus D tablets are taken once each week. Choose the day of the week that best fits your schedule. Every week, take one Fosamax Plus D tablet on your chosen day.

Take the Fosamax Plus D tablet first thing in the morning, at least 30 minutes before you eat or drink anything or take any other medicine.

Take the tablet with a full glass (6 to 8 ounces) of water. Use only plain water (not mineral water) when taking this medicine.

Do not crush, chew, or suck the tablet. Swallow the pill whole.

After taking an Fosamax Plus D tablet, carefully follow these instructions:

Do not lie down or recline for at least 30 minutes after taking Fosamax Plus D. Do not eat or drink anything other than plain water. Do not take any other medicines including vitamins, calcium, or antacids for at least 30 minutes after taking Fosamax Plus D. It may be best to take your other medicines at a different time of the day. Talk with your doctor about the best dosing schedule for your other medicines.

To be sure this medication is helping your condition, your bone mineral density will need to be tested on a regular basis. You may not need to take Fosamax Plus D for longer than 3 to 5 years if you take it for osteoporosis.

If you need to have any dental work (especially surgery), tell the dentist ahead of time that you are using Fosamax Plus D. You may need to stop using the medicine for a short time.

Fosamax Plus D is only part of a complete program of treatment that may also include diet changes, exercise, and taking calcium and vitamin supplements. Follow your diet, medication, and exercise routines very closely.

Store at room temperature away from moisture and heat.

Detailed Fosamax Plus D dosage information


Seek emergency medical attention or call the Poison Help line at 1-800-222-1222. Drink a full glass of milk and call your local poison control center or emergency room right away. Do not make yourself vomit and do not lie down.

Overdose symptoms may include muscle cramps, numbness or tingling, tight muscles in your face, seizure (convulsions), irritability, and unusual thoughts or behavior.


Store at room temperature between 15 and 30 degrees C (59 and 86 degrees F) away from moisture and heat. Throw away any unused medicine after the expiration date. Keep out of the reach of children.

Side effects

The most common side effects associated with Fosamax are:

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Side effect occurrence does not only depend on medication you are taking, but also on your overall health and other factors.


Do not take any other medicines including vitamins, calcium, or antacids for at least 30 minutes after taking Fosamax Plus D.

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The results show that mobility can both reduce and enhance the ability to track climate change that a narrow range can severely reduce this ability and that population range and total population size can both increase and decrease under a moving climate. We examined an upper abdominal phantom using a Somatom Definition Flash CT-Scanner (Siemens, Forchheim, Germany). Clinical situations falling outside existing mhGAP modules inspired the development of supplemental treatment protocols. The isolated lignin was then purified and undergone elemental analysis. This case was unusual as the disease had extended beyond the ear and we therefore wish to alert clinicians to cholesteatoma as a possible cause of facial swelling. Laboratory evaluation, genetic mutation analysis, bilateral gonadectomy, and hormone replacement.

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As an experimental model, we used Rat-1A fibroblasts that form vascular tumors upon transformation by Myc in immunocompromised mice. The chemical process allows the development of glass-ceramic powder at 600 degrees C which is the goal of the present paper. Department of Obstetrics and Gynaecology, Robert Ballanger Hospital, Aulnay-sous-Bois, France. These data indicate that Sna4p has two functional motifs, one for interaction with the AP-3 complex, followed by entry into the ALP pathway, and one for binding Rsp5p, which directs the protein to the MVB pathway. Relationship between tolerance to GABAA agonist and bursting properties in neocortical neurons during GABA-withdrawal syndrome. In vivo pharmacokinetics and organ distribution studies were performed to check the efficiency of the delivery system. Migration patterns have caused these conditions to be seen all around the world, not only in developing countries. In in vivo study, rats with R3230 breast adenocarcinoma were sacrificed 24 h post-treatment and gross coagulation areas were compared, and next, randomized into four treatment arms (control, quercetin alone, RF alone, and combination) for Kaplan-Meier analysis of defined endpoint survival.

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