Friday, September 30, 2016

Carbaglu


Generic Name: carglumic acid (kar GLOO mik AS id)

Brand Names: Carbaglu


What is carglumic acid?

Carglumic acid is a man-made form of an enzyme that occurs naturally in the liver. This enzyme is necessary for processing excess nitrogen produced when the body metabolizes proteins. Without this enzyme, nitrogen builds up in the form of ammonia and is not removed from the body. Ammonia is very toxic when it circulates in blood and tissues and can cause permanent brain damage, coma, or death.


Carglumic acid is used to treat hyperammonemia (HYE-per-AM-moe-NEE-mee-a), a urea cycle disorder caused by lack of a certain liver enzyme. Carglumic acid is usually given with other medications to treat this lifelong disorder.


Carglumic acid may also be used for purposes not listed in this medication guide.


What is the most important information I should know about carglumic acid?


Avoid eating foods that are high in protein when you first start taking carglumic acid. Follow your doctor's instructions about any other restrictions on food, beverages, or activity.

Your doctor may occasionally change your dose to make sure you get the best results. Dose adjustments are especially important as your child grows.


To be sure this medicine is helping your condition and is not causing harmful effects, your blood will need to be tested often. A buildup of ammonia in the blood can quickly cause brain injury or death. Do not miss any follow up visits to your doctor for blood tests. Every person with a urea cycle disorder should remain under the care of a doctor.

If you skip a meal, do not take your dose of carglumic acid. Wait until your next meal.


Carglumic acid is only part of a complete program of treatment that may also include a special diet and other medications. It is very important to follow the diet plan created for you by your doctor or nutrition counselor. You should become very familiar with the list of foods you should eat or avoid to help control your condition.

What should I discuss with my healthcare provider before taking carglumic acid?


Tell your doctor about all of your medical conditions.


Carglumic acid is only part of a complete program of treatment that may also include a special diet and other medications. It is very important to follow the diet plan created for you by your doctor or nutrition counselor. You should become very familiar with the list of foods you should eat or avoid to help control your condition. FDA pregnancy category C. It is not known whether carglumic acid will harm an unborn baby. Tell your doctor if you are pregnant or plan to become pregnant while using this medication. It is not known whether carglumic acid passes into breast milk or if it could harm a nursing baby. You should not breast-feed while you are using carglumic acid.

How should I take carglumic acid?


Take exactly as prescribed by your doctor. Do not take in larger or smaller amounts or for longer than recommended. Follow the directions on your prescription label.


Your doctor may occasionally change your dose to make sure you get the best results. Dose adjustments are especially important as your child grows.


Carglumic acid is usually taken 2 to 4 times each day, just before each meal or feeding. Follow your doctor's instructions.


Do not chew, crush, or swallow the carglumic acid tablet whole. Place it into a glass of water and allow the tablet to disperse in the liquid. The tablet will not dissolve completely. Drink this mixture right away. To make sure you get the entire dose, add a little more liquid to the same glass, swirl gently and drink right away.

The carglumic acid tablet may be taken with an oral syringe as follows: Place a 200-milligram tablet into an oral syringe and draw 2.5 milliliters of water into the syringe. Shake until the tablet is dispersed and then empty the syringe into your mouth. Refill the syringe with water, shake gently, and empty into your mouth.


The carglumic acid tablet can also be given through a nasogastric (NG) feeding tube as follows: Disperse the tablet in an oral syringe as directed above. Attach the syringe to the NG tube and push the plunger down to empty the syringe into the tube. Then flush the tube with more water to wash the contents down.


To be sure this medicine is helping your condition and is not causing harmful effects, your blood will need to be tested often. A buildup of ammonia in the blood can quickly cause brain injury or death. Do not miss any follow up visits to your doctor for blood tests. Every person with a urea cycle disorder should remain under the care of a doctor. Store unopened bottles of carglumic acid tablets in the refrigerator, do not freeze. After opening the bottle, store at room temperature away from moisture and heat. Do not store opened bottles in the refrigerator. Keep the bottle tightly closed when not in use.

When you open the bottle, write the date on the bottle. Throw away any unused tablets 1 month (30 days) after the date of opening, or if the expiration date printed on the label has passed.


What happens if I miss a dose?


Take the missed dose as soon as you remember, but only if you are getting ready to eat a meal. Skip the missed dose if it is almost time for your next scheduled dose. Do not take extra medicine to make up the missed dose.


If you skip a meal, do not take your dose of carglumic acid. Wait until your next meal.


What happens if I overdose?


Seek emergency medical attention or call the Poison Help line at 1-800-222-1222.

Overdose symptoms may include fever, heavy sweating, fast heart rate, coughing up mucus, and feeling restless.


What should I avoid while taking carglumic acid?


Avoid eating foods that are high in protein when you first start taking carglumic acid.

Follow your doctor's instructions about any other restrictions on food, beverages, or activity.


Carglumic acid side effects


Get emergency medical help if you have any of these signs of an allergic reaction: hives; difficult breathing; swelling of your face, lips, tongue, or throat. Call your doctor at once if you have a serious side effect such as:

  • fever, chills, body aches, flu symptoms, sores in your mouth and throat;




  • pale skin, feeling light-headed or short of breath, rapid heart rate, trouble concentrating; or




  • pain or fullness in your ear, hearing problems.



Less serious side effects may include:



  • vomiting, diarrhea, stomach pain;




  • headache; or




  • stuffy nose, sore throat.



This is not a complete list of side effects and others may occur. Call your doctor for medical advice about side effects. You may report side effects to FDA at 1-800-FDA-1088.


What other drugs will affect carglumic acid?


There may be other drugs that can interact with carglumic acid. Tell your doctor about all the prescription and over-the-counter medications you use. This includes vitamins, minerals, herbal products, and drugs prescribed by other doctors. Do not start using a new medication without telling your doctor.



More Carbaglu resources


  • Carbaglu Side Effects (in more detail)
  • Carbaglu Use in Pregnancy & Breastfeeding
  • Carbaglu Support Group
  • 0 Reviews for Carbaglu - Add your own review/rating


  • Carbaglu Consumer Overview

  • Carbaglu MedFacts Consumer Leaflet (Wolters Kluwer)

  • Carbaglu Prescribing Information (FDA)

  • carglumic acid Advanced Consumer (Micromedex) - Includes Dosage Information

  • Carglumic Acid Professional Patient Advice (Wolters Kluwer)



Compare Carbaglu with other medications


  • Hyperammonemia


Where can I get more information?


  • Your pharmacist can provide more information about carglumic acid.

See also: Carbaglu side effects (in more detail)


Celontin


Generic Name: methsuximide (meth SUX i mide)

Brand Names: Celontin


What is Celontin (methsuximide)?

Methsuximide is an anti-epileptic medication, also called an anticonvulsant.


Methsuximide is used alone or in combination with other medications to treat absence seizures (also called "petit mal" seizures) in adults and children.


Methsuximide may also be used for purposes not listed in this medication guide.


What is the most important information I should know about Celontin (methsuximide)?


Methsuximide can cause a decrease in many types of blood cells (white cells, red cells, platelets). Call your doctor at once if you have any unusual bleeding, weakness, or any signs of infection, even if these symptoms first occur after you have been using the medication for several months.

Methsuximide may also cause liver damage. Call your doctor if you have symptoms such as loss of appetite, stomach pain, or jaundice (yellowing of the skin or eyes).


You may have thoughts about suicide while taking this medication. Your doctor will need to check you at regular visits. Do not miss any scheduled appointments.


Report any new or worsening symptoms to your doctor, such as: mood or behavior changes, anxiety, panic attacks, trouble sleeping, or if you feel impulsive, irritable, agitated, hostile, aggressive, restless, hyperactive (mentally or physically), depressed, or have thoughts about suicide or hurting yourself.


Do not stop using methsuximide without first talking to your doctor, even if you feel fine. You may have increased seizures if you stop using methsuximide suddenly. You may need to use less and less before you stop the medication completely.

Contact your doctor if your seizures get worse or you have them more often while taking methsuximide.


Wear a medical alert tag or carry an ID card stating that you take methsuximide. Any doctor, dentist, or emergency medical care provider who treats you should know that you take seizure medication.

What should I discuss with my healthcare provider before taking Celontin (methsuximide)?


You should not use this medication if you are allergic to methsuximide or to other seizure medications.

To make sure you can safely take methsuximide, tell your doctor if you have any of these other conditions:



  • lupus;




  • liver disease;




  • kidney disease; or




  • a history of depression, mental illness, or suicidal thoughts or actions.



You may have thoughts about suicide while taking this medication. Tell your doctor if you have new or worsening depression or suicidal thoughts during the first several months of treatment, or whenever your dose is changed.


Your family or other caregivers should also be alert to changes in your mood or symptoms. Your doctor will need to check you at regular visits. Do not miss any scheduled appointments.


It is not known whether methsuximide will harm an unborn baby. Tell your doctor if you are pregnant or plan to become pregnant while using this medication. Although methsuximide might harm an unborn baby, having a seizure during pregnancy could harm both mother and baby. If you become pregnant while taking methsuximide, do not stop taking it without your doctor's advice. If you are pregnant, your name may be listed on a pregnancy registry. This is to track the outcome of the pregnancy and to evaluate any effects of methsuximide on the baby. It is not known whether methsuximide passes into breast milk or if it could harm a nursing baby. Do not use this medication without telling your doctor if you are breast-feeding a baby.

How should I take Celontin (methsuximide)?


Take exactly as prescribed by your doctor. Do not take in larger or smaller amounts or for longer than recommended. Follow the directions on your prescription label.


Methsuximide can lower blood cells that help your body fight infections. This can make it easier for you to bleed from an injury or get sick from being around others who are ill. Your blood may need to be tested often. Visit your doctor regularly.

Call your doctor at once if you have any unusual bleeding, weakness, or any signs of infection, including flu-like symptoms. These symptoms may first develop even after you have been using the medication for several months.


Do not stop using methsuximide without first talking to your doctor, even if you feel fine. You may have increased seizures if you stop using methsuximide suddenly. You may need to use less and less before you stop the medication completely.

Contact your doctor if your seizures get worse or you have them more often while taking methsuximide.


Wear a medical alert tag or carry an ID card stating that you take methsuximide. Any medical care provider who treats you should know that you take seizure medication.

Use methsuximide regularly to get the most benefit. Get your prescription refilled before you run out of medicine completely.


Store at room temperature away from moisture, heat, and light. High heat can cause a methsuximide capsule to melt.

See also: Celontin dosage (in more detail)

What happens if I miss a dose?


Take the missed dose as soon as you remember. Skip the missed dose if it is almost time for your next scheduled dose. Do not take extra medicine to make up the missed dose.


What happens if I overdose?


Seek emergency medical attention or call the Poison Help line at 1-800-222-1222.

Overdose symptoms may include vomiting, extreme drowsiness, and weak or shallow breathing.


What should I avoid while taking Celontin (methsuximide)?


Methsuximide can cause side effects that may impair your thinking or reactions. Be careful if you drive or do anything that requires you to be awake and alert. Drinking alcohol can increase certain drowsiness or dizziness caused by methsuximide.

Celontin (methsuximide) side effects


Get emergency medical help if you have any of these signs of an allergic reaction: hives; difficult breathing; swelling of your face, lips, tongue, or throat.

Report any new or worsening symptoms to your doctor, such as: mood or behavior changes, anxiety, panic attacks, trouble sleeping, or if you feel impulsive, irritable, agitated, hostile, aggressive, restless, hyperactive (mentally or physically), depressed, or have thoughts about suicide or hurting yourself.


Call your doctor at once if you have a serious side effect such as:

  • signs of infection such as fever, chills, sore throat, flu symptoms, easy bruising or bleeding (nosebleeds, bleeding gums), mouth sores, feeling very weak or tired;




  • signs of liver damage, such as nausea, stomach pain, low fever, loss of appetite, dark urine, clay-colored stools, jaundice (yellowing of the skin or eyes);




  • joint pain or swelling with fever, swollen glands, muscle aches, chest pain;




  • patchy skin color, red spots, or a butterfly-shaped skin rash over your cheeks and nose (worsens in sunlight);




  • severe skin reaction -- fever, sore throat, swelling in your face or tongue, burning in your eyes, skin pain, followed by a red or purple skin rash that spreads (especially in the face or upper body) and causes blistering and peeling; or




  • worsening of seizures.



Less serious side effects may include:



  • diarrhea, constipation;




  • stomach pain, nausea, weight loss;




  • dizziness, drowsiness, nervousness, confusion;




  • headache;




  • blurred vision; or




  • loss of balance or coordination.



This is not a complete list of side effects and others may occur. Call your doctor for medical advice about side effects. You may report side effects to FDA at 1-800-FDA-1088.


What other drugs will affect Celontin (methsuximide)?


Cold or allergy medicine, sedatives, narcotic pain medicine, sleeping pills, muscle relaxers, and medicine for depression or anxiety can add to sleepiness caused by methsuximide. Tell your doctor if you regularly use any of these medicines..

Tell your doctor about all other seizure medication you use, especially:



  • phenobarbital (Luminal, Solfoton); or




  • phenytoin (Dilantin).



This list is not complete and other drugs may interact with methsuximide. Tell your doctor about all medications you use. This includes prescription, over-the-counter, vitamin, and herbal products. Do not start a new medication without telling your doctor.



More Celontin resources


  • Celontin Side Effects (in more detail)
  • Celontin Dosage
  • Celontin Use in Pregnancy & Breastfeeding
  • Drug Images
  • Celontin Drug Interactions
  • Celontin Support Group
  • 0 Reviews for Celontin - Add your own review/rating


  • Celontin MedFacts Consumer Leaflet (Wolters Kluwer)

  • Celontin Prescribing Information (FDA)

  • methsuximide Advanced Consumer (Micromedex) - Includes Dosage Information

  • Methsuximide Professional Patient Advice (Wolters Kluwer)



Compare Celontin with other medications


  • Seizures


Where can I get more information?


  • Your pharmacist can provide more information about methsuximide.

See also: Celontin side effects (in more detail)


Conjugated Estrogens/Medroxyprogesterone


Pronunciation: KON-joo-GAY-ted ES-troe-jenz/me-DROX-ee-proe-JES-ter-one
Generic Name: Conjugated Estrogens/Medroxyprogesterone
Brand Name: Examples include Premphase and Prempro

Do not use Conjugated Estrogens/Medroxyprogesterone to prevent heart disease, heart attacks, strokes, or dementia. Conjugated Estrogens/Medroxyprogesterone may increase the risk of heart disease (including heart attack), stroke, dementia, serious blood clots in the lung or leg, or breast cancer. Talk with your doctor regularly about whether you still need treatment with Conjugated Estrogens/Medroxyprogesterone.





Conjugated Estrogens/Medroxyprogesterone is used for:

Treating menopausal symptoms (eg, hot flashes, vaginal dryness). If you are only being treated for vaginal menopause symptoms, products applied locally, such as vaginal creams, tablets, or rings, should be considered before products taken by mouth or absorbed through the skin. Conjugated Estrogens/Medroxyprogesterone is also used to prevent bone loss (osteoporosis) in women at high risk.


Conjugated Estrogens/Medroxyprogesterone is a combination of estrogen and progestin hormones. It works by replacing these hormones in the body when the body does not make enough on its own.


Do NOT use Conjugated Estrogens/Medroxyprogesterone if:


  • you are allergic to any ingredient in Conjugated Estrogens/Medroxyprogesterone

  • you are pregnant or think you may be pregnant

  • you have abnormal vaginal bleeding, an estrogen-dependent tumor, a history of blood clots, circulation problems, active/recent stroke or heart attack, or liver disease

  • you have or have had breast, uterine, ovarian, or vaginal cancer; or have had a hysterectomy (removal of the uterus)

Contact your doctor or health care provider right away if any of these apply to you.



Before using Conjugated Estrogens/Medroxyprogesterone:


Some medical conditions may interact with Conjugated Estrogens/Medroxyprogesterone. Tell your doctor or pharmacist if you have any medical conditions, especially if any of the following apply to you:


  • if you are pregnant, planning to become pregnant, or are breast-feeding

  • if you are taking any prescription or nonprescription medicine, herbal preparation, or dietary supplement

  • if you have allergies to medicines, foods, or other substances

  • if you have a family history of breast cancer or have had an abnormal breast mammogram or x-ray, a noncancerous lump on the breast, or bone cancer

  • if you have asthma, diabetes, seizures, dementia, migraine headaches, heart disease (eg, high blood pressure, heart attacks, heart failure), kidney disease, an underactive thyroid, lupus, pancreatitis, or abnormal calcium levels in the blood

  • if you have depression, uterus problems (eg, uterine fibroids, endometriosis), cholesterol or lipid problems, gallbladder disease, excessive weight gain, or a blood disorder (eg, porphyria), or if you are significantly overweight

  • if you have had high blood pressure during pregnancy or yellowing of the skin or eyes during pregnancy or with past estrogen use

  • if you are scheduled for surgery or will be on bed rest

  • if you smoke cigarettes or use tobacco

Some MEDICINES MAY INTERACT with Conjugated Estrogens/Medroxyprogesterone. Tell your health care provider if you are taking any other medicines, especially any of the following:


  • Aminogluthethimide, hydantoins (eg, phenytoin), or rifampin because they may decrease Conjugated Estrogens/Medroxyprogesterone's effectiveness

  • Anticoagulants (eg, warfarin) because their effectiveness may be decreased or their risk of side effects may be increased by Conjugated Estrogens/Medroxyprogesterone

  • Corticosteroids (eg, prednisone) or succinylcholine because the risk of their side effects may be increased by Conjugated Estrogens/Medroxyprogesterone

This may not be a complete list of all interactions that may occur. Ask your health care provider if Conjugated Estrogens/Medroxyprogesterone may interact with other medicines that you take. Check with your health care provider before you start, stop, or change the dose of any medicine.


How to use Conjugated Estrogens/Medroxyprogesterone:


Use Conjugated Estrogens/Medroxyprogesterone as directed by your doctor. Check the label on the medicine for exact dosing instructions.


  • An extra patient leaflet is available with Conjugated Estrogens/Medroxyprogesterone. Talk to your pharmacist if you have questions about this information.

  • Take Conjugated Estrogens/Medroxyprogesterone by mouth with food or right after a meal to prevent stomach upset.

  • Conjugated Estrogens/Medroxyprogesterone works best if it is taken at the same time each day.

  • Continue to take Conjugated Estrogens/Medroxyprogesterone even if you feel well. Do not miss any doses.

  • If you miss a dose of Conjugated Estrogens/Medroxyprogesterone, take it as soon as possible. If it is almost time for your next dose, skip the missed dose and go back to your regular dosing schedule. Do not take 2 doses at once.

Ask your health care provider any questions you may have about how to use Conjugated Estrogens/Medroxyprogesterone.



Important safety information:


  • Conjugated Estrogens/Medroxyprogesterone may cause dizziness or lightheadedness. These effects may be worse if you take it with alcohol or certain medicines. Use Conjugated Estrogens/Medroxyprogesterone with caution. Do not drive or perform other possibly unsafe tasks until you know how you react to it.

  • Conjugated Estrogens/Medroxyprogesterone may cause dark skin patches on your face (melasma). Exposure to the sun may make these patches darker. If patches develop, consult your doctor about the use of sunscreen or protective clothing when your skin is exposed to the sun, sunlamps, or tanning booths.

  • Conjugated Estrogens/Medroxyprogesterone may increase the risk of stroke, heart attack, blood clots, high blood pressure, or similar problems. The risk may be greater if you smoke (especially in women older than 35 years of age).

  • You should talk to your doctor about instructions for examining your own breasts, and report any lumps to your doctor immediately.

  • Before you have surgery or will be confined to a chair or bed for a long period of time (eg, a long plane flight), talk to your doctor about your use of Conjugated Estrogens/Medroxyprogesterone.

  • Tell your doctor or dentist that you take Conjugated Estrogens/Medroxyprogesterone before you receive any medical or dental care, emergency care, or surgery.

  • Conjugated Estrogens/Medroxyprogesterone may interfere with certain lab tests. Be sure your doctors and lab personnel know that you are using Conjugated Estrogens/Medroxyprogesterone.

  • Diabetes patients - Conjugated Estrogens/Medroxyprogesterone may affect your blood sugar. Check blood sugar levels closely. Ask your doctor before you change the dose of your diabetes medicine.

  • Lab tests, including blood pressure monitoring and Pap smears, may be performed while you use Conjugated Estrogens/Medroxyprogesterone. These tests may be used to monitor your condition or check for side effects. Be sure to keep all doctor and lab appointments.

  • Use Conjugated Estrogens/Medroxyprogesterone with caution in the ELDERLY; they may be more sensitive to its effects.

  • Conjugated Estrogens/Medroxyprogesterone should not be used in CHILDREN; safety and effectiveness in children have not been confirmed.

  • PREGNANCY and BREAST-FEEDING: Do not use Conjugated Estrogens/Medroxyprogesterone if you are pregnant. If you think you may be pregnant, contact your doctor right away. Conjugated Estrogens/Medroxyprogesterone is found in breast milk. Do not breast-feed while using Conjugated Estrogens/Medroxyprogesterone.


Possible side effects of Conjugated Estrogens/Medroxyprogesterone:


All medicines may cause side effects, but many people have no, or minor, side effects. Check with your doctor if any of these most COMMON side effects persist or become bothersome:



Abnormal hair growth; bloating; breast tenderness or pain; changes in sleep patterns; darkening of the skin; dizziness; fatigue; hair loss; headache; irritability; increased or decreased sex drive; lightheadedness; nausea; stomach cramps; stomach upset; weight changes.



Seek medical attention right away if any of these SEVERE side effects occur:

Severe allergic reactions (rash; hives; itching; difficulty breathing; tightness in the chest; swelling of the mouth, face, lips, or tongue); breast lumps; calf pain or swelling; changes in vaginal bleeding (eg, spotting, breakthrough bleeding, prolonged bleeding); chest pain; faintness; leg pain; mental or mood changes (eg, severe depression, memory loss); one-sided weakness; shortness of breath; slurred speech; sudden severe headache; swelling of hands or feet; unusual vaginal discharge, itching, or odor; vision changes; vomiting; yellowing of the skin or eyes.



This is not a complete list of all side effects that may occur. If you have questions about side effects, contact your health care provider. Call your doctor for medical advice about side effects. To report side effects to the appropriate agency, please read the Guide to Reporting Problems to FDA.


See also: Conjugated Estrogens/Medroxyprogesterone side effects (in more detail)


If OVERDOSE is suspected:


Contact 1-800-222-1222 (the American Association of Poison Control Centers), your local poison control center, or emergency room immediately. Symptoms may include excessive vaginal bleeding; severe nausea and vomiting.


Proper storage of Conjugated Estrogens/Medroxyprogesterone:

Store Conjugated Estrogens/Medroxyprogesterone at room temperature, between 68 and 77 degrees F (20 and 20 degrees C). Brief storage at temperatures between 59 and 86 degrees F (15 and 30 degrees C) is permitted. Store away from heat, moisture, and light. Do not store in the bathroom. Keep Conjugated Estrogens/Medroxyprogesterone out of the reach of children and away from pets.


General information:


  • If you have any questions about Conjugated Estrogens/Medroxyprogesterone, please talk with your doctor, pharmacist, or other health care provider.

  • Conjugated Estrogens/Medroxyprogesterone is to be used only by the patient for whom it is prescribed. Do not share it with other people.

  • If your symptoms do not improve or if they become worse, check with your doctor.

  • Check with your pharmacist about how to dispose of unused medicine.

This information is a summary only. It does not contain all information about Conjugated Estrogens/Medroxyprogesterone. If you have questions about the medicine you are taking or would like more information, check with your doctor, pharmacist, or other health care provider.



Issue Date: February 1, 2012

Database Edition 12.1.1.002

Copyright © 2012 Wolters Kluwer Health, Inc.

More Conjugated Estrogens/Medroxyprogesterone resources


  • Conjugated Estrogens/Medroxyprogesterone Side Effects (in more detail)
  • Conjugated Estrogens/Medroxyprogesterone Use in Pregnancy & Breastfeeding
  • Conjugated Estrogens/Medroxyprogesterone Drug Interactions
  • Conjugated Estrogens/Medroxyprogesterone Support Group
  • 6 Reviews for Conjugated Estrogens/Medroxyprogesterone - Add your own review/rating


Compare Conjugated Estrogens/Medroxyprogesterone with other medications


  • Atrophic Urethritis
  • Atrophic Vaginitis
  • Oophorectomy
  • Osteoporosis
  • Postmenopausal Symptoms
  • Primary Ovarian Failure

Fosamax




Generic Name: alendronate sodium

Dosage Form: tablets, oral solution
Fosamax®

(ALENDRONATE SODIUM) TABLETS AND ORAL SOLUTION

Fosamax Description


Fosamax® (alendronate sodium) is a bisphosphonate that acts as a specific inhibitor of osteoclast-mediated bone resorption. Bisphosphonates are synthetic analogs of pyrophosphate that bind to the hydroxyapatite found in bone.


Alendronate sodium is chemically described as (4-amino-1-hydroxybutylidene) bisphosphonic acid monosodium salt trihydrate.


The empirical formula of alendronate sodium is C4H12NNaO7P2•3H2O and its formula weight is 325.12. The structural formula is:



Alendronate sodium is a white, crystalline, nonhygroscopic powder. It is soluble in water, very slightly soluble in alcohol, and practically insoluble in chloroform.


Tablets Fosamax for oral administration contain 6.53, 13.05, 45.68, 52.21 or 91.37 mg of alendronate monosodium salt trihydrate, which is the molar equivalent of 5, 10, 35, 40 and 70 mg, respectively, of free acid, and the following inactive ingredients: microcrystalline cellulose, anhydrous lactose, croscarmellose sodium, and magnesium stearate. Tablets Fosamax 10 mg also contain carnauba wax.


Each bottle of the oral solution contains 91.35 mg of alendronate monosodium salt trihydrate, which is the molar equivalent to 70 mg of free acid. Each bottle also contains the following inactive ingredients: sodium citrate dihydrate and citric acid anhydrous as buffering agents, sodium saccharin, artificial raspberry flavor, and purified water. Added as preservatives are sodium propylparaben 0.0225% and sodium butylparaben 0.0075%.



Fosamax - Clinical Pharmacology



Mechanism of Action


Animal studies have indicated the following mode of action. At the cellular level, alendronate shows preferential localization to sites of bone resorption, specifically under osteoclasts. The osteoclasts adhere normally to the bone surface but lack the ruffled border that is indicative of active resorption. Alendronate does not interfere with osteoclast recruitment or attachment, but it does inhibit osteoclast activity. Studies in mice on the localization of radioactive [3H]alendronate in bone showed about 10-fold higher uptake on osteoclast surfaces than on osteoblast surfaces. Bones examined 6 and 49 days after [3H]alendronate administration in rats and mice, respectively, showed that normal bone was formed on top of the alendronate, which was incorporated inside the matrix. While incorporated in bone matrix, alendronate is not pharmacologically active. Thus, alendronate must be continuously administered to suppress osteoclasts on newly formed resorption surfaces. Histomorphometry in baboons and rats showed that alendronate treatment reduces bone turnover (i.e., the number of sites at which bone is remodeled). In addition, bone formation exceeds bone resorption at these remodeling sites, leading to progressive gains in bone mass.



Pharmacokinetics


Absorption

Relative to an intravenous (IV) reference dose, the mean oral bioavailability of alendronate in women was 0.64% for doses ranging from 5 to 70 mg when administered after an overnight fast and two hours before a standardized breakfast. Oral bioavailability of the 10 mg tablet in men (0.59%) was similar to that in women when administered after an overnight fast and 2 hours before breakfast.


Fosamax 70 mg oral solution and Fosamax 70 mg tablet are equally bioavailable.


A study examining the effect of timing of a meal on the bioavailability of alendronate was performed in 49 postmenopausal women. Bioavailability was decreased (by approximately 40%) when 10 mg alendronate was administered either 0.5 or 1 hour before a standardized breakfast, when compared to dosing 2 hours before eating. In studies of treatment and prevention of osteoporosis, alendronate was effective when administered at least 30 minutes before breakfast.


Bioavailability was negligible whether alendronate was administered with or up to two hours after a standardized breakfast. Concomitant administration of alendronate with coffee or orange juice reduced bioavailability by approximately 60%.


Distribution

Preclinical studies (in male rats) show that alendronate transiently distributes to soft tissues following 1 mg/kg IV administration but is then rapidly redistributed to bone or excreted in the urine. The mean steady-state volume of distribution, exclusive of bone, is at least 28 L in humans. Concentrations of drug in plasma following therapeutic oral doses are too low (less than 5 ng/mL) for analytical detection. Protein binding in human plasma is approximately 78%.


Metabolism

There is no evidence that alendronate is metabolized in animals or humans.


Excretion

Following a single IV dose of [14C]alendronate, approximately 50% of the radioactivity was excreted in the urine within 72 hours and little or no radioactivity was recovered in the feces. Following a single 10 mg IV dose, the renal clearance of alendronate was 71 mL/min (64, 78; 90% confidence interval [CI]), and systemic clearance did not exceed 200 mL/min. Plasma concentrations fell by more than 95% within 6 hours following IV administration. The terminal half-life in humans is estimated to exceed 10 years, probably reflecting release of alendronate from the skeleton. Based on the above, it is estimated that after 10 years of oral treatment with Fosamax (10 mg daily) the amount of alendronate released daily from the skeleton is approximately 25% of that absorbed from the gastrointestinal tract.


Special Populations

Pediatric:


The oral bioavailability in children was similar to that observed in adults; however, Fosamax is not indicated for use in children (see PRECAUTIONS, Pediatric Use).



Gender:


Bioavailability and the fraction of an IV dose excreted in urine were similar in men and women.



Geriatric:


Bioavailability and disposition (urinary excretion) were similar in elderly and younger patients. No dosage adjustment is necessary (see DOSAGE AND ADMINISTRATION).



Race:


Pharmacokinetic differences due to race have not been studied.



Renal Insufficiency:


Preclinical studies show that, in rats with kidney failure, increasing amounts of drug are present in plasma, kidney, spleen, and tibia. In healthy controls, drug that is not deposited in bone is rapidly excreted in the urine. No evidence of saturation of bone uptake was found after 3 weeks dosing with cumulative IV doses of 35 mg/kg in young male rats. Although no clinical information is available, it is likely that, as in animals, elimination of alendronate via the kidney will be reduced in patients with impaired renal function. Therefore, somewhat greater accumulation of alendronate in bone might be expected in patients with impaired renal function.


No dosage adjustment is necessary for patients with mild-to-moderate renal insufficiency (creatinine clearance 35 to 60 mL/min). Fosamax is not recommended for patients with more severe renal insufficiency (creatinine clearance <35 mL/min) due to lack of experience with alendronate in renal failure.



Hepatic Insufficiency:


As there is evidence that alendronate is not metabolized or excreted in the bile, no studies were conducted in patients with hepatic insufficiency. No dosage adjustment is necessary.



Drug Interactions


(also see PRECAUTIONS, Drug Interactions)


Intravenous ranitidine was shown to double the bioavailability of oral alendronate. The clinical significance of this increased bioavailability and whether similar increases will occur in patients given oral H2-antagonists is unknown.


In healthy subjects, oral prednisone (20 mg three times daily for five days) did not produce a clinically meaningful change in the oral bioavailability of alendronate (a mean increase ranging from 20 to 44%).


Products containing calcium and other multivalent cations are likely to interfere with absorption of alendronate.



Pharmacodynamics


Alendronate is a bisphosphonate that binds to bone hydroxyapatite and specifically inhibits the activity of osteoclasts, the bone-resorbing cells. Alendronate reduces bone resorption with no direct effect on bone formation, although the latter process is ultimately reduced because bone resorption and formation are coupled during bone turnover.



Osteoporosis in postmenopausal women


Osteoporosis is characterized by low bone mass that leads to an increased risk of fracture. 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 (spinal) fracture. Osteoporosis occurs in both males and females but is most common among women following the menopause, when bone turnover increases and the rate of bone resorption exceeds that of bone formation. These changes result in progressive bone loss and lead to osteoporosis in a significant proportion of women over age 50. Fractures, usually of the spine, hip, and wrist, are the common consequences. From age 50 to age 90, the risk of hip fracture in white women increases 50-fold and the risk of vertebral fracture 15- to 30-fold. It is estimated that approximately 40% of 50-year-old women will sustain one or more osteoporosis-related fractures of the spine, hip, or wrist during their remaining lifetimes. Hip fractures, in particular, are associated with substantial morbidity, disability, and mortality.


Daily oral doses of alendronate (5, 20, and 40 mg for six weeks) in postmenopausal women produced biochemical changes indicative of dose-dependent inhibition of bone resorption, including decreases in urinary calcium and urinary markers of bone collagen degradation (such as deoxypyridinoline and cross-linked N-telopeptides of type I collagen). These biochemical changes tended to return toward baseline values as early as 3 weeks following the discontinuation of therapy with alendronate and did not differ from placebo after 7 months.


Long-term treatment of osteoporosis with Fosamax 10 mg/day (for up to five years) reduced urinary excretion of markers of bone resorption, deoxypyridinoline and cross-linked N-telopeptides of type l collagen, by approximately 50% and 70%, respectively, to reach levels similar to those seen in healthy premenopausal women. Similar decreases were seen in patients in osteoporosis prevention studies who received Fosamax 5 mg/day. The decrease in the rate of bone resorption indicated by these markers was evident as early as one month and at three to six months reached a plateau that was maintained for the entire duration of treatment with Fosamax. In osteoporosis treatment studies Fosamax 10 mg/day decreased the markers of bone formation, osteocalcin and bone specific alkaline phosphatase by approximately 50%, and total serum alkaline phosphatase by approximately 25 to 30% to reach a plateau after 6 to 12 months. In osteoporosis prevention studies Fosamax 5 mg/day decreased osteocalcin and total serum alkaline phosphatase by approximately 40% and 15%, respectively. Similar reductions in the rate of bone turnover were observed in postmenopausal women during one-year studies with once weekly Fosamax 70 mg for the treatment of osteoporosis and once weekly Fosamax 35 mg for the prevention of osteoporosis. These data indicate that the rate of bone turnover reached a new steady-state, despite the progressive increase in the total amount of alendronate deposited within bone.


As a result of inhibition of bone resorption, asymptomatic reductions in serum calcium and phosphate concentrations were also observed following treatment with Fosamax. In the long-term studies, reductions from baseline in serum calcium (approximately 2%) and phosphate (approximately 4 to 6%) were evident the first month after the initiation of Fosamax 10 mg. No further decreases in serum calcium were observed for the five-year duration of treatment; however, serum phosphate returned toward prestudy levels during years three through five. Similar reductions were observed with Fosamax 5 mg/day. In one-year studies with once weekly Fosamax 35 and 70 mg, similar reductions were observed at 6 and 12 months. The reduction in serum phosphate may reflect not only the positive bone mineral balance due to Fosamax but also a decrease in renal phosphate reabsorption.



Osteoporosis in men


Treatment of men with osteoporosis with Fosamax 10 mg/day for two years reduced urinary excretion of cross-linked N-telopeptides of type I collagen by approximately 60% and bone-specific alkaline phosphatase by approximately 40%. Similar reductions were observed in a one-year study in men with osteoporosis receiving once weekly Fosamax 70 mg.



Glucocorticoid-induced Osteoporosis


Sustained use of glucocorticoids is commonly associated with development of osteoporosis and resulting fractures (especially vertebral, hip, and rib). It occurs both in males and females of all ages. Osteoporosis occurs as a result of inhibited bone formation and increased bone resorption resulting in net bone loss. Alendronate decreases bone resorption without directly inhibiting bone formation.


In clinical studies of up to two years' duration, Fosamax 5 and 10 mg/day reduced cross-linked N-telopeptides of type I collagen (a marker of bone resorption) by approximately 60% and reduced bone-specific alkaline phosphatase and total serum alkaline phosphatase (markers of bone formation) by approximately 15 to 30% and 8 to 18%, respectively. As a result of inhibition of bone resorption, Fosamax 5 and 10 mg/day induced asymptomatic decreases in serum calcium (approximately 1 to 2%) and serum phosphate (approximately 1 to 8%).



Paget's disease of bone


Paget's disease of bone is a chronic, focal skeletal disorder characterized by greatly increased and disorderly bone remodeling. Excessive osteoclastic bone resorption is followed by osteoblastic new bone formation, leading to the replacement of the normal bone architecture by disorganized, enlarged, and weakened bone structure.


Clinical manifestations of Paget's disease range from no symptoms to severe morbidity due to bone pain, bone deformity, pathological fractures, and neurological and other complications. Serum alkaline phosphatase, the most frequently used biochemical index of disease activity, provides an objective measure of disease severity and response to therapy.


Fosamax decreases the rate of bone resorption directly, which leads to an indirect decrease in bone formation. In clinical trials, Fosamax 40 mg once daily for six months produced significant decreases in serum alkaline phosphatase as well as in urinary markers of bone collagen degradation. As a result of the inhibition of bone resorption, Fosamax induced generally mild, transient, and asymptomatic decreases in serum calcium and phosphate.



Clinical Studies


Treatment of osteoporosis

Postmenopausal women



Effect on bone mineral density

The efficacy of Fosamax 10 mg once daily in postmenopausal women, 44 to 84 years of age, with osteoporosis (lumbar spine bone mineral density [BMD] of at least 2 standard deviations below the premenopausal mean) was demonstrated in four double-blind, placebo-controlled clinical studies of two or three years' duration. These included two three-year, multicenter studies of virtually identical design, one performed in the United States (U.S.) and the other in 15 different countries (Multinational), which enrolled 478 and 516 patients, respectively. The following graph shows the mean increases in BMD of the lumbar spine, femoral neck, and trochanter in patients receiving Fosamax 10 mg/day relative to placebo-treated patients at three years for each of these studies.


Osteoporosis Treatment Studies in Postmenopausal Women: Increase in BMD: Fosamax 10mg/day at Three Years



At three years significant increases in BMD, relative both to baseline and placebo, were seen at each measurement site in each study in patients who received Fosamax 10 mg/day. Total body BMD also increased significantly in each study, suggesting that the increases in bone mass of the spine and hip did not occur at the expense of other skeletal sites. Increases in BMD were evident as early as three months and continued throughout the three years of treatment. (See figures below for lumbar spine results.) In the two-year extension of these studies, treatment of 147 patients with Fosamax 10 mg/day resulted in continued increases in BMD at the lumbar spine and trochanter (absolute additional increases between years 3 and 5: lumbar spine, 0.94%; trochanter, 0.88%). BMD at the femoral neck, forearm and total body were maintained. Fosamax was similarly effective regardless of age, race, baseline rate of bone turnover, and baseline BMD in the range studied (at least 2 standard deviations below the premenopausal mean).


Osteoporosis Treatment Studies in Postmenopausal Women: Time Course of Effect of Fosamax 10 mg/day Versus Placebo: Lumbar Spine BMD Percent Change From Baseline



In patients with postmenopausal osteoporosis treated with Fosamax 10 mg/day for one or two years, the effects of treatment withdrawal were assessed. Following discontinuation, there were no further increases in bone mass and the rates of bone loss were similar to those of the placebo groups.


The therapeutic equivalence of once weekly Fosamax 70 mg (n=519) and Fosamax 10 mg daily (n=370) was demonstrated in a one-year, double-blind, multicenter study of postmenopausal women with osteoporosis. In the primary analysis of completers, the mean increases from baseline in lumbar spine BMD at one year were 5.1% (4.8, 5.4%; 95% CI) in the 70-mg once-weekly group (n=440) and 5.4% (5.0, 5.8%; 95% CI) in the 10-mg daily group (n=330). The two treatment groups were also similar with regard to BMD increases at other skeletal sites. The results of the intention-to-treat analysis were consistent with the primary analysis of completers.



Effect on fracture incidence

Data on the effects of Fosamax on fracture incidence are derived from three clinical studies: 1) U.S. and Multinational combined: a study of patients with a BMD T-score at or below minus 2.5 with or without a prior vertebral fracture, 2) Three-Year Study of the Fracture Intervention Trial (FIT): a study of patients with at least one baseline vertebral fracture, and 3) Four-Year Study of FIT: a study of patients with low bone mass but without a baseline vertebral fracture.


To assess the effects of Fosamax on the incidence of vertebral fractures (detected by digitized radiography; approximately one third of these were clinically symptomatic), the U.S. and Multinational studies were combined in an analysis that compared placebo to the pooled dosage groups of Fosamax (5 or 10 mg for three years or 20 mg for two years followed by 5 mg for one year). There was a statistically significant reduction in the proportion of patients treated with Fosamax experiencing one or more new vertebral fractures relative to those treated with placebo (3.2% vs. 6.2%; a 48% relative risk reduction). A reduction in the total number of new vertebral fractures (4.2 vs. 11.3 per 100 patients) was also observed. In the pooled analysis, patients who received Fosamax had a loss in stature that was statistically significantly less than was observed in those who received placebo (-3.0 mm vs. -4.6 mm).


The Fracture Intervention Trial (FIT) consisted of two studies in postmenopausal women: the Three-Year Study of patients who had at least one baseline radiographic vertebral fracture and the Four-Year Study of patients with low bone mass but without a baseline vertebral fracture. In both studies of FIT, 96% of randomized patients completed the studies (i.e., had a closeout visit at the scheduled end of the study); approximately 80% of patients were still taking study medication upon completion.



Fracture Intervention Trial: Three-Year Study (patients with at least one baseline radiographic vertebral fracture)

This randomized, double-blind, placebo-controlled, 2027-patient study (Fosamax, n=1022; placebo, n=1005) demonstrated that treatment with Fosamax resulted in statistically significant reductions in fracture incidence at three years as shown in the table below.


























































Effect of Fosamax on Fracture Incidence in the Three-Year Study of FIT (patients with vertebral fracture at baseline)
Percent of Patients
Fosamax

(n=1022)
Placebo

(n=1005)
Absolute

Reduction

in Fracture

Incidence
Relative

Reduction in Fracture

Risk %

*

Number evaluable for vertebral fractures: Fosamax, n=984; placebo, n=966


p<0.001


p=0.007

§

p<0.01


p<0.05

Patients with:
Vertebral fractures (diagnosed by X-ray)*
     ≥ 1 new vertebral fracture7.915.07.147
     ≥ 2 new vertebral fractures0.54.94.490
Clinical (symptomatic) fractures
     Any clinical (symptomatic) fracture13.818.14.326
     ≥ 1 clinical (symptomatic) vertebral fracture2.35.02.754§
Hip fracture1.12.21.151
Wrist (forearm) fracture2.24.11.948

Furthermore, in this population of patients with baseline vertebral fracture, treatment with Fosamax significantly reduced the incidence of hospitalizations (25.0% vs. 30.7%).


In the Three-Year Study of FIT, fractures of the hip occurred in 22 (2.2%) of 1005 patients on placebo and 11 (1.1%) of 1022 patients on Fosamax, p=0.047. The figure below displays the cumulative incidence of hip fractures in this study.


Cumulative Incidence of Hip Fractures in the Three-Year Study of FIT (patients with radiographic vertebral fracture at baseline)




Fracture Intervention Trial: Four-Year Study (patients with low bone mass but without a baseline radiographic vertebral fracture)

This randomized, double-blind, placebo-controlled, 4432-patient study (Fosamax, n=2214; placebo, n=2218) further investigated the reduction in fracture incidence due to Fosamax. The intent of the study was to recruit women with osteoporosis, defined as a baseline femoral neck BMD at least two standard deviations below the mean for young adult women. However, due to subsequent revisions to the normative values for femoral neck BMD, 31% of patients were found not to meet this entry criterion and thus this study included both osteoporotic and non-osteoporotic women. The results are shown in the table below for the patients with osteoporosis.


























































Effect of Fosamax on Fracture Incidence in Osteoporotic* Patients in the Four-Year Study of FIT (patients without vertebral fracture at baseline)
Percent of Patients
Fosamax

(n=1545)
Placebo

(n=1521)
Absolute

Reduction

in Fracture

Incidence
Relative

Reduction in Fracture Risk (%)

*

Baseline femoral neck BMD at least 2 SD below the mean for young adult women


Number evaluable for vertebral fractures: Fosamax, n=1426; placebo, n=1428


p<0.001

§

p=0.035


p=0.01

#

Not significant. This study was not powered to detect differences at these sites.

Patients with:
Vertebral fractures (diagnosed by X-ray)
     ≥ 1 new vertebral fracture2.54.82.348
     ≥ 2 new vertebral fractures0.10.60.578§
Clinical (symptomatic) fractures
     Any clinical (symptomatic) fracture12.916.23.322
     ≥ 1 clinical (symptomatic) vertebral fracture1.01.60.641(NS)#
Hip fracture1.01.40.429 (NS)#
Wrist (forearm) fracture3.93.8-0.1NS#

Fracture results across studies

In the Three-Year Study of FIT, Fosamax reduced the percentage of women experiencing at least one new radiographic vertebral fracture from 15.0% to 7.9% (47% relative risk reduction, p<0.001); in the Four-Year Study of FIT, the percentage was reduced from 3.8% to 2.1% (44% relative risk reduction, p=0.001); and in the combined U.S./Multinational studies, from 6.2% to 3.2% (48% relative risk reduction, p=0.034).


Fosamax reduced the percentage of women experiencing multiple (two or more) new vertebral fractures from 4.2% to 0.6% (87% relative risk reduction, p<0.001) in the combined U.S./Multinational studies and from 4.9% to 0.5% (90% relative risk reduction, p<0.001) in the Three-Year Study of FIT. In the Four-Year Study of FIT, Fosamax reduced the percentage of osteoporotic women experiencing multiple vertebral fractures from 0.6% to 0.1% (78% relative risk reduction, p=0.035).


Thus, Fosamax reduced the incidence of radiographic vertebral fractures in osteoporotic women whether or not they had a previous radiographic vertebral fracture.


Fosamax, over a three- or four-year period, was associated with statistically significant reductions in loss of height vs. placebo in patients with and without baseline radiographic vertebral fractures. At the end of the FIT studies the between-treatment group differences were 3.2 mm in the Three-Year Study and 1.3 mm in the Four-Year Study.



Bone histology

Bone histology in 270 postmenopausal patients with osteoporosis treated with Fosamax at doses ranging from 1 to 20 mg/day for one, two, or three years revealed normal mineralization and structure, as well as the expected decrease in bone turnover relative to placebo. These data, together with the normal bone histology and increased bone strength observed in rats and baboons exposed to long-term alendronate treatment, support the conclusion that bone formed during therapy with Fosamax is of normal quality.



Men


The efficacy of Fosamax in men with hypogonadal or idiopathic osteoporosis was demonstrated in two clinical studies.


A two-year, double-blind, placebo-controlled, multicenter study of Fosamax 10 mg once daily enrolled a total of 241 men between the ages of 31 and 87 (mean, 63). All patients in the trial had either: 1) a BMD T-score ≤-2 at the femoral neck and ≤-1 at the lumbar spine, or 2) a baseline osteoporotic fracture and a BMD T-score ≤-1 at the femoral neck. At two years, the mean increases relative to placebo in BMD in men receiving Fosamax 10 mg/day were significant at the following sites: lumbar spine, 5.3%; femoral neck, 2.6%; trochanter, 3.1%; and total body, 1.6%. Treatment with Fosamax also reduced height loss (Fosamax, -0.6 mm vs. placebo, -2.4 mm).


A one-year, double-blind, placebo-controlled, multicenter study of once weekly Fosamax 70 mg enrolled a total of 167 men between the ages of 38 and 91 (mean, 66). Patients in the study had either: 1) a BMD T-score ≤-2 at the femoral neck and ≤-1 at the lumbar spine, 2) a BMD T-score ≤-2 at the lumbar spine and ≤-1 at the femoral neck, or 3) a baseline osteoporotic fracture and a BMD T-score ≤-1 at the femoral neck. At one year, the mean increases relative to placebo in BMD in men receiving Fosamax 70 mg once weekly were significant at the following sites: lumbar spine, 2.8%; femoral neck, 1.9%; trochanter, 2.0%; and total body, 1.2%. These increases in BMD were similar to those seen at one year in the 10 mg once-daily study.


In both studies, BMD responses were similar regardless of age (≥65 years vs. <65 years), gonadal function (baseline testosterone <9 ng/dL vs. ≥9 ng/dL), or baseline BMD (femoral neck and lumbar spine T-score ≤-2.5 vs. >-2.5).


Prevention of osteoporosis in postmenopausal women

Prevention of bone loss was demonstrated in two double-blind, placebo-controlled studies of postmenopausal women 40-60 years of age. One thousand six hundred nine patients (Fosamax 5 mg/day; n=498) who were at least six months postmenopausal were entered into a two-year study without regard to their baseline BMD. In the other study, 447 patients (Fosamax 5 mg/day; n=88), who were between six months and three years postmenopause, were treated for up to three years. In the placebo-treated patients BMD losses of approximately 1% per year were seen at the spine, hip (femoral neck and trochanter) and total body. In contrast, Fosamax 5 mg/day prevented bone loss in the majority of patients and induced significant increases in mean bone mass at each of these sites (see figures below). In addition, Fosamax 5 mg/day reduced the rate of bone loss at the forearm by approximately half relative to placebo. Fosamax 5 mg/day was similarly effective in this population regardless of age, time since menopause, race and baseline rate of bone turnover.


Osteoporosis Prevention Studies in Postmenopausal Women



The therapeutic equivalence of once weekly Fosamax 35 mg (n=362) and Fosamax 5 mg daily (n=361) was demonstrated in a one-year, double-blind, multicenter study of postmenopausal women without osteoporosis. In the primary analysis of completers, the mean increases from baseline in lumbar spine BMD at one year were 2.9% (2.6, 3.2%; 95% CI) in the 35-mg once-weekly group (n=307) and 3.2% (2.9, 3.5%; 95% CI) in the 5-mg daily group (n=298). The two treatment groups were also similar with regard to BMD increases at other skeletal sites. The results of the intention-to-treat analysis were consistent with the primary analysis of completers.



Bone histology


Bone histology was normal in the 28 patients biopsied at the end of three years who received Fosamax at doses of up to 10 mg/day.


Concomitant use with estrogen/hormone replacement therapy (HRT)

The effects on BMD of treatment with Fosamax 10 mg once daily and conjugated estrogen (0.625 mg/day) either alone or in combination were assessed in a two-year, double-blind, placebo-controlled study of hysterectomized postmenopausal osteoporotic women (n=425). At two years, the increases in lumbar spine BMD from baseline were significantly greater with the combination (8.3%) than with either estrogen or Fosamax alone (both 6.0%).


The effects on BMD when Fosamax was added to stable doses (for at least one year) of HRT (estrogen ± progestin) were assessed in a one-year, double-blind, placebo-controlled study in postmenopausal osteoporotic women (n=428). The addition of Fosamax 10 mg once daily to HRT produced, at one year, significantly greater increases in lumbar spine BMD (3.7%) vs. HRT alone (1.1%).


In these studies, significant increases or favorable trends in BMD for combined therapy compared with HRT alone were seen at the total hip, femoral neck, and trochanter. No significant effect was seen for total body BMD.


Histomorphometric studies of transiliac biopsies in 92 subjects showed normal bone architecture. Compared to placebo there was a 98% suppression of bone turnover (as assessed by mineralizing surface) after 18 months of combined treatment with Fosamax and HRT, 94% on Fosamax alone, and 78% on HRT alone. The long-term effects of combined Fosamax and HRT on fracture occurrence and fracture healing have not been studied.


Glucocorticoid-induced osteoporosis

The efficacy of Fosamax 5 and 10 mg once daily in men and women receiving glucocorticoids (at least 7.5 mg/day of prednisone or equivalent) was demonstrated in two, one-year, double-blind, randomized, placebo-controlled, multicenter studies of virtually identical design, one performed in the United States and the other in 15 different countries (Multinational [which also included Fosamax 2.5 mg/day]). These studies enrolled 232 and 328 patients, respectively, between the ages of 17 and 83 with a variety of glucocorticoid-requiring diseases. Patients received supplemental calcium and vitamin D. The following figure shows the mean increases relative to placebo in BMD of the lumbar spine, femoral neck, and trochanter in patients receiving Fosamax 5 mg/day for each study.


Studies in Glucocorticoid-Treated Patients: Increase in BMD: Fosamax 5 mg/day at One Year



After one year, significant increases relative to placebo in BMD were seen in the combined studies at each of these sites in patients who received Fosamax 5 mg/day. In the placebo-treated patients, a significant decrease in BMD occurred at the femoral neck (-1.2%), and smaller decreases were seen at the lumbar spine and trochanter. Total body BMD was maintained with Fosamax 5 mg/day. The increases in BMD with Fosamax 10 mg/day were similar to those with Fosamax 5 mg/day in all patients except for postmenopausal women not receiving estrogen therapy. In these women, the increases (relative to placebo) with Fosamax 10 mg/day were greater than those with Fosamax 5 mg/day at the lumbar spine (4.1% vs. 1.6%) and trochanter (2.8% vs. 1.7%), but not at other sites. Fosamax was effective regardless of dose or duration of glucocorticoid use. In addition, Fosamax was similarly effective regardless of age (<65 vs. ≥65 years), race (Caucasian vs. other races), gender, underlying disease, baseline BMD, baseline bone turnover, and use with a variety of common medications.


Bone histology was normal in the 49 patients biopsied at the end of one year who received Fosamax at doses of up to 10 mg/day.


Of the original 560 patients in these studies, 208 patients who remained on at least 7.5 mg/day of prednisone or equivalent continued into a one-year double-blind extension. After two years of treatment, spine BMD increased by 3.7% and 5.0% relative to placebo with Fosamax 5 and 10 mg/day, respectively. Significant increases in BMD (relative to placebo) were also observed at the femoral neck, trochanter, and total body.


After one year, 2.3% of patients treated with Fosamax 5 or 10 mg/day (pooled) vs. 3.7% of those treated with placebo experienced a new vertebral fracture (not significant). However, in the population studied for two years, treatment with Fosamax (pooled dosage groups: 5 or 10 mg for two years or 2.5 mg for one year followed by 10 mg for one year) significantly reduced the incidence of patients with a new vertebral fracture (Fosamax 0.7% vs. placebo 6.8%).


Paget's disease of bone

The efficacy of Fosamax 40 mg once daily for six months was demonstrated in two double-blind clinical studies of male and female patients with moderate to severe Paget's disease (alkaline phosphatase at least twice the upper limit of normal): a placebo-controlled, multinational study and a U.S. comparative study with etidronate disodium 400 mg/day. The following figure shows the mean percent changes from baseline in serum alkaline phosphatase for up to six months of randomized treatment.


Studies in Paget's Disease of Bone: Effect on Serum Alkaline Phosphatase of Fosamax 40 mg/day Versus Placebo or Etidronate 400 mg/day



At six months the suppression in alkaline phosphatase in patients treated with Fosamax was significantly greater than that achieved with etidronate and contrasted with the complete lack of response in placebo-treated patients. Response (defined as either normalization of serum alkaline phosphatase or decrease from baseline ≥60%) occurred in approximately 85% of patients treated with Fosamax in the combined studies vs. 30% in the etidronate group and 0% in the placebo group. Fosamax was similarly effective regardless of age, gender, race, prior use of other bisphosphonates, or baseline alkaline phosphatase within the range studied (at least twice the upper limit of normal).


Bone histology was evaluated in 33 patients with Paget's disease treated with Fosamax 40 mg/day for 6 months. As in patients treated for osteoporosis (see Clinical Studies, Treatment of osteoporosis in postmenopausal women, Bone histology), Fosamax did not impair mineralization, and the expected decrease in the rate of bone turnover was observed. Normal lamellar bone was produced during treatment with Fosamax, even where preexisting bone was woven and disorganized. Overall, bone histology data support the conclusion that bone formed during treatment with Fosamax is of normal quality.



Animal Pharmacology


The relative inhibitory activities on bone resorption and mineralization of alendronate and etidronate were compared in the Schenk assay, which is based on histological examination of the epiphyses of growing rats. In this assay, the lowest dose of alendronate that interfered with bone mineralization (leading to osteomalacia) was 6000-fold the antiresorptive dose. The corresponding ratio for etidronate was one to one. These data suggest that alendronate administered in therapeutic doses is highly unlikely to induce osteomalacia.



Indications and Usage for Fosamax


Fosamax is indicated for:


  • Treatment and prevention of osteoporosis in postmenopausal women

    • For the treatment of osteoporosis, Fosamax increases bone mass and reduces the incidence of fractures, including those of the hip and spine (vertebral compression fractures). Osteoporosis may be confirmed by the finding of low bone mass (for example, at least 2 standard deviations below the premenopausal mean) or by the presence or history of osteoporotic fracture. (See CLINICAL PHARMACOLOGY, Pharmacodynamics.)


    • For the pr

Isuprel


Isuprel is a brand name of isoproterenol, approved by the FDA in the following formulation(s):


ISUPREL (isoproterenol hydrochloride - injectable; injection)



  • Manufacturer: HOSPIRA

    Approved Prior to Jan 1, 1982

    Strength(s): 0.2MG/ML [RLD][AP]

Has a generic version of Isuprel been approved?


Yes. The following products are equivalent to Isuprel:


isoproterenol hydrochloride injectable; injection



  • Manufacturer: INTL MEDICATION

    Approved Prior to Jan 1, 1982

    Strength(s): 0.2MG/ML [AP]

Note: Fraudulent online pharmacies may attempt to sell an illegal generic version of Isuprel. These medications may be counterfeit and potentially unsafe. If you purchase medications online, be sure you are buying from a reputable and valid online pharmacy. Ask your health care provider for advice if you are unsure about the online purchase of any medication.

See also: About generic drugs.




Related Patents

There are no current U.S. patents associated with Isuprel.

See also...

  • Isuprel Consumer Information (Wolters Kluwer)
  • Isoproterenol Consumer Information (Wolters Kluwer)
  • Isoproterenol inhalation Consumer Information (Cerner Multum)
  • Isoproterenol Hydrochloride AHFS DI Monographs (ASHP)

Thursday, September 29, 2016

Indium Oxyquinoline





Dosage Form: Solution

For the Radiolabeling of Autologous Leukocytes


Rx ONLY


Diagnostic—For intravenous use

For single dose, single use only



Indium Oxyquinoline Description


Indium In 111 oxyquinoline (oxine) is a diagnostic radiopharmaceutical intended for radiolabeling autologous leukocytes. It is supplied as a sterile, non-pyrogenic, isotonic aqueous solution with a pH range of 6.5 to 7.5. Each mL of the solution contains 37 MBq, 1 mCi of indium In 111 [no carrier added, >1.85 GBq/µg indium (>50 mCi/µg indium)] at calibration time, 50 µg oxyquinoline, 100 µg polysorbate 80, and 6 mg of HEPES (N-2-hydroxyethylpiperazine-N'-2-ethane sulfonic acid) buffer in 0.75% sodium chloride solution. The drug is intended for single use only and contains no bacteriostatic agent. The radionuclidic impurity limit for indium 114m is not greater than 37 kBq, 1 µCi of indium 114m per 37 MBq, 1 mCi of indium In 111 at the time of calibration. The radionuclidic composition at expiration time is not less than 99.75% of indium In 111 and not more than 0.25% of indium In 114m/114.


Chemical name: Indium In 111 Oxyquinoline.


The precise structure of the indium In 111 oxyquinoline complex is unknown at this time. The empirical formula is (C9H6NO)3 In 111.



PHYSICAL CHARACTERISTICS


Indium In 111 decays by electron capture with a physical half-life of 67.2 hours (2.8 days). The energies of the photons that are useful for detection and imaging studies are listed in Table 1.













Table 1. Principal Radiation Emission Data*
RadiationMean %/

Disintegration
Mean Energy

(keV)

*

Kocher, David C., "Radioactive Decay Data Tables", DOE/TIC-11026, 115 (1981).

Gamma 290.2171.3
Gamma 394245.4

EXTERNAL RADIATION


The exposure rate constant for 37 MBq, 1 mCi indium In 111 is 8.3 × 10-4 C/kg/h (3.21 R/h) at 1 cm. The first half value thickness of lead (Pb) for indium In 111 is 0.023 cm. A range of values for the relative attenuation of the radiation emitted by this radionuclide that results from the interposition of various thicknesses of Pb is shown in Table 2. For example, the use of 0.834 cm of lead will decrease the external radiation exposure by a factor of about 1,000.
















Table 2. Radiation Attenuation by Lead Shielding*
Shield Thickness

(Pb) cm
Coefficient of

Attenuation

*

Data supplied by Oak Ridge Associated Universities, Radiopharmaceutical Internal Dose Information Center, 1984.

0.0230.5
0.20310-1
0.51310-2
0.83410-3
1.12  10-4

These estimates of attenuation do not take into consideration the presence of longer-lived contaminants with higher energy photons, namely indium In 114m/114.


To allow correction for physical decay of indium In 111, the fractions that remain at selected intervals before and after the time of calibration are shown in Table 3.
























Table 3. Physical Decay Chart for Indium In 111, Half-life 67.2 hours
DayFraction RemainingDayFraction Remaining

*

Calibration Time

-21.64120.610
-11.28130.476
  0*1.00040.372
10.78150.290

Indium Oxyquinoline - Clinical Pharmacology



Indium forms a saturated (1:3) complex with oxyquinoline. The complex is neutral and lipid-soluble, which enables it to penetrate the cell membrane. Within the cell, indium becomes firmly attached to cytoplasmic components; the liberated oxyquinoline is released by the cell. It is thought likely that the mechanism of labeling cells with indium In 111 oxyquinoline involves an exchange reaction between the oxyquinoline carrier and subcellular components which chelate indium more strongly than oxyquinoline. The low stability constant of the oxyquinoline complex, estimated at approximately 10, supports this theory.


Following the recommended leukocyte cell labeling procedure, approximately 77% of the added indium In 111 oxyquinoline is incorporated in the resulting cell pellet (which represents approximately 3-4 × 108 WBC).


Cell clumping can occur and was found in about one fifth of the leukocyte preparations examined. The presence of red blood cells or plasma will lead to reduced leukocyte labeling efficiency. Transferrin in plasma competes for indium In 111 oxyquinoline.


After injection of labeled leukocytes into normal volunteers, about 30% of the dose is taken up by spleen and 30% by liver, reaching a plateau at 2-48 hours after injection. No significant clearance of radioactivity is observed at 72 hours in these two organs. Pulmonary uptake is 4-7.5% at 10 minutes but is lost rapidly; pulmonary radioactivity is usually visible in scans only up to about 4 hours after injection.


The human biodistribution studies in three normal subjects injected with indium In 111 oxyquinoline labeled leukocytes indicate a biexponential disappearance of indium In 111 from the blood when monitored for up to 72 hours. Between 9.5 to 24.4% of the injected dose remains in whole blood and clears with a biological half-time of 2.8 to 5.5 hours. The remainder (13-18%) clears from blood with a biological half-time of 64 to 116 hours.


Elimination from the body of injected indium In 111 oxyquinoline is probably mainly through decay to stable cadmium since only a negligible amount (less than 1%) of the dose is excreted in feces and urine in 24 hours.


Clearance from whole blood and biological distribution can vary considerably with the individual recipient, the condition of the injected cells and labeling techniques used.


Release of radioactivity from the labeled cells is about 3% at 1 hour and 24% at 24 hours.


Clearance from liver and spleen, for the purpose of calculating the radiation dose, is assumed to be equal to the physical half-life of indium In 111 (67.2 hours).



Indications and Usage for Indium Oxyquinoline


Indium In 111 oxyquinoline is indicated for radiolabeling autologous leukocytes.


Indium In 111 oxyquinoline labeled leukocytes may be used as an adjunct in the detection of inflammatory processes to which leukocytes migrate, such as those associated with abscesses or other infection, following reinjection and detection by appropriate imaging procedures. The degree of accuracy may vary with labeling techniques and with the size, location and nature of the inflammatory process.


Indium In 111 oxyquinoline labeled leukocyte imaging is not the preferred technique for the initial evaluation of patients with a high clinical probability of an abscess in a known location. Ultrasound or computed tomography may provide a better anatomical delineation of the infectious process and information may be obtained more quickly than with labeled leukocytes. If localization by these techniques is successful, labeled leukocytes should not be used as a confirmatory procedure. If localization or diagnosis by these methods fails or is ambiguous, indium In 111 oxyquinoline labeled leukocyte imaging may be appropriate.



Contraindications


None known.



Warnings


The content of the vial of indium In 111 oxyquinoline solution is intended only for use in the preparation of indium In 111 oxyquinoline labeled autologous leukocytes, and is not to be administered directly. Autologous leukocyte labeling is not recommended in leukopenic patients because of the small number of available leukocytes.


Due to radiation exposure, indium In 111 oxyquinoline labeled leukocytes could cause fetal harm when administered to pregnant women. If this radiopharmaceutical is used during pregnancy, the patient should be informed of the potential hazard to the fetus.


Indium In 111 oxyquinoline labeled autologous leukocytes should be used only when the benefit to be obtained exceeds the risks involved in children under eighteen years of age owing to the high radiation burden and the potential for delayed manifestation of long-term adverse effects.



Precautions


Clumping of cells may produce focal accumulations of radioactivity in lungs which do not wash out in 24 hours and thus may lead to false positive results. This phenomenon can be detected by imaging the chest immediately after injection.


The normally high uptake of indium In 111 oxyquinoline labeled leukocytes by spleen and liver may mask inflammatory lesions in these organs. Labeled leukocytes have been observed to accumulate in the colon and accessory spleens of patients with or without disease.


Chemotaxis of granulocytes deteriorates during storage and loss of chemotaxis may cause false negative scans. The spontaneous release of indium In 111 has been reported to range from about 3% at one hour to 24% at 24 hours [ten Berge, R.J.M., Natarajan, A.T., Hardeman, M.R., et al, Labeling with indium In 111 has detrimental effects on human lymphocytes, Journal of Nuclear Medicine, 24, 615-620 (1983)]. The maximum amount of time recommended between drawing the blood and reinjection should not exceed 5 hours. It is recommended that the labeled cells be used within one hour of preparation, if possible and in no case more than three hours after preparation.


Plasma and red cell contamination impairs labeling efficiency of leukocytes. Hemolyzed blood in labeled leukocytes may produce heart pool activity and should be avoided.


Cell aggregates of various degrees have been reported. Cell labeling techniques and standing of cell preparation may be contributing factors.


Nuclear medicine procedures involving withdrawal and reinjection of blood have the potential for transmission of blood borne pathogens. Procedures should be implemented to avoid administration errors and viral contamination of personnel during blood product labeling. A system of checks similar to the ones used for administering blood transfusions should be routine.



General


Strict aseptic techniques should be used to maintain sterility throughout the procedures for using this product.


Do not use after the expiration time and date (5 days after calibration time) stated on the label.


The contents of the vial are radioactive. Adequate shielding of the preparation must be maintained at all times.


Indium In 111 oxyquinoline, like other radioactive drugs, must be handled with care and appropriate safety measures should be used to minimize radiation exposure to clinical personnel. Care should also be taken to minimize radiation exposure to the patient consistent with proper patient management.


Radiopharmaceuticals should be used only by physicians who are qualified by training and experience in the safe use and handling of radionuclides and whose experience and training have been approved by the appropriate governmental agency authorized to license the use of radio-nuclides.



Carcinogenesis, Mutagenesis, Impairment of Fertility


Although earlier studies suggested that oxyquinoline (oxine) might have carcinogenic potential, recent studies have found no evidence of carcinogenicity in either rats or mice given oxyquinoline in feed at concentrations of 1,500 or 3,000 ppm for 103 weeks.


It has been reported [ten Berge, R.J.M., Natarajan, A.T., Hardeman, M.R., et al, Labeling with indium In 111 has detrimental effects on human lymphocytes, Journal of Nuclear Medicine, 24, 615-620 (1983)] that human lymphocytes labeled with recommended concentrations of indium In 111 oxyquinoline showed chromosome aberrations consisting of gaps, breaks and exchanges that appear to be radiation induced. At 555 kBq/107, 15 µCi/107 lymphocytes 93% of the cells were reported to be abnormal. The oncogenic potential of such lymphocytes has not been studied. It has been reported that the radiation dose to 108 leukocytes is 9 × 104 mGy (0.9 × 104 rads) from 18.5 MBq, 500 µCi [Goodwin, David A., Cell labeling with oxine chelates of radioactive metal ions: Techniques and clinical implications, Journal of Nuclear Medicine, 19, 557-559 (1978)].


Studies have not been performed to evaluate whether indium In 111 oxyquinoline affects fertility in male or female laboratory animals or humans.



Pregnancy Category C


Animal reproduction studies have not been conducted with Indium In 111 Oxyquinoline labeled leukocytes. It is also not known whether Indium In 111 Oxyquinoline labeled leukocytes can cause fetal harm when administered to a pregnant woman or can affect reproduction capacity.


However, Indium Nitrate, a closely related compound, was teratogenic and embryopathic in hamsters. Indium In 111 Oxyquinoline labeled leukocytes should be given to a pregnant woman only if clearly needed.


Ideally, examinations using radiopharmaceuticals, especially those elective in nature, in women of childbearing capability should be performed during the first few (approximately ten) days following the onset of menses.



Nursing Mothers


It is reported that indium 111 is secreted in human milk following administration of indium In 111 labeled leukocytes. Therefore, formula feedings should be substituted for breast feedings.



Pediatric Use


Safety and effectiveness in pediatric patients below age 18 have not been established (See Warnings).



Adverse Reactions


Sensitivity reactions (urticaria) have been reported. The presence of fever may mask pyrogenic reactions from indium In 111 oxyquinoline labeled leukocytes. The possibility of delayed adverse reactions has not been studied.



Indium Oxyquinoline Dosage and Administration


The recommended adult (70 kg) dose of indium In 111 oxyquinoline labeled autologous leukocytes is 7.4 to 18.5 MBq, 200-500 µCi. Indium In 111 oxyquinoline solution is intended for the radiolabeling of autologous leukocytes. The indium In 111 oxyquinoline labeled autologous leukocytes are administered intravenously.


Imaging is recommended at approximately 24 hours post injection. Typically, anterior and posterior views of the chest, abdomen and pelvis should be obtained with other views as required.


Aseptic procedures and a shielded syringe should be employed in the withdrawal of indium In 111 oxyquinoline from the vial. Similar procedures should be employed during the labeling procedure and the administration of the labeled leukocytes to the patient. The user should wear waterproof gloves during the entire procedure. The patient's dose should be measured by a suitable radioactivity calibration system immediately before administration. At this time, the leukocyte preparation should be checked for gross clumping and red blood cell contamination.



RADIATION DOSIMETRY


The estimated absorbed radiation doses to an adult patient weighing 70 kg from an intravenous dose of 18.5 MBq, 500 µCi of indium In 111 oxyquinoline labeled leukocytes including contributions from indium In 114m/114 as a radionuclidic impurity are shown in Table 4.


















































































Table 4. Radiation Dose Estimate in a 70 kg Human for 18.5 MBq, 500 µCi at Expiry of Indium In 111 (99.75%) Oxyquinoline labeled leukocytes with Indium In 114m/114 (0.25%)
Assumptions: 30% to spleen, 30% to liver, 34% to red marrow, 6% to remainder of body, with no excretion.
OrganmGy/18.5 MBq

In 111
Rads/500 µCi

In 111
Spleen13013
Liver191.9
Red Marrow131.3
Skeleton3.640.364
Testes0.10.01
Ovaries1.90.19
Total Body3.10.31
 
OrganmGy/46.25 kBq

In 114m/114
Rads/1.25 µCi

In 114m/114
Spleen707
Liver7.10.71
Red Marrow6.90.69
Skeleton0.850.085
Testes0.040.004
Ovaries0.060.006
Total Body0.60.06
 
OrganTotal Dose

in mGy
Total Dose

in Rads
Spleen20020
Liver26.62.66
Red Marrow19.91.99
Skeleton4.50.45
Testes0.140.014
Ovaries2.00.2
Total Body3.70.37

The dose of radiation absorbed by the organs will vary with the distribution of the blood cells in the organs, which in turn will depend on the predominance of the cell types labeled and their condition.



LABELING PROCEDURE


Sterile technique must be used throughout. It is important that all equipment used for the preparation of reagents be thoroughly cleaned to assure the absence of trace metal impurities. The user should wear waterproof gloves during the handling and administration procedure.


  1. The following equipment is recommended:

    One (1) 60 mL or two (2) 30 mL sterile disposable plastic syringes with a 19 or 20 gauge needle (NOTE: Do not use a smaller gauge needle).

    Ring stand and clamp(s).

    Three (3) 50 mL sterile conical plastic centrifuge tubes with screw caps. Label each set with patient ID and "WBC", "LPP" and "Wash" respectively (NOTE: 3 centrifuge tubes per patient).

    Clinical Centrifuge with horizontal, 4 place rotor or equivalent.

    Sodium Chloride 0.9% Injection, USP.

    Three (3) disposable 5 or 10 mL syringes and 19 gauge needles.

    Syringe shield to dispense indium In 111 oxyquinoline.

    A dose calibrator.

    Butterfly catheter infusion set.

    Test tube rack.

    Lab timer.

    10 mL syringe with a 19 gauge or 20 gauge needle.

    19 gauge needle with filter (optional).

  2. Withdraw from the patient 30-50 mL blood [preferably fifty (50) mL] using aseptic venipuncture technique using the 60 mL syringe fitted with a 19 gauge or 20 gauge needle and containing approximately 1000-1500 units heparin in 1-2 mL. Blood withdrawal should be smooth and slow so as not to produce bubbles or foaming.

  3. Remove and dispose of the needle and replace with a syringe cap. Gently mix the contents of the syringe and label with the patient's ID, date and time.

  4. Upon receipt of the full syringe for processing, the contents should again be gently mixed.

  5. Clamp the syringe barrel to the ring stand in an upright (needle side up) position and tilt the syringe 10-20 degrees from its position perpendicular to the bench.

  6. Allow the red cells to sediment 30-60 minutes, depending upon when the supernatant [leukocyte rich plasma (LRP)] looks clear of red blood cells.

  7. Replace the syringe cap with an infusion set.

  8. Collect the plasma (LRP) in the centrifuge tube marked "WBC" by expressing the LRP through the catheter tubing making sure not to get any red cells into the WBC tube.

  9. Immediately centrifuge the capped WBC tube at 400-450 g for 5 minutes.

  10. Transfer the supernatant to the leukocyte poor plasma (LPP) tube leaving behind 0.5-1.0 mL supernatant to cover the white cell button (NOTE: the button often contains a small number of red cells and may appear red).

  11. Wash the white cell button with 4-6 mL Sodium Chloride (0.9%) Injection, USP. Resuspend the button by gentle swirling.

  12. Centrifuge the capped WBC tube at 400-450 g for 5 minutes (alternatively, 150 g for 8 minutes) and discard all but 0.5-1.0 mL of the supernate to cover the cells.

  13. Add 5.0 mL Sodium Chloride (0.9%) Injection, USP. Resuspend the cells by gentle swirling.

  14. With the shielded syringe, draw up approximately 22.2 MBq, 600 µCi indium In 111 oxyquinoline. Check the amount of radioactivity in a dose calibrator set for indium In 111 and record for labeling efficiency calculations.

    Parenteral drug products should be inspected visually for particulate matter and discoloration before administration.

  15. In several additions, add the indium In 111 oxyquinoline to the WBC tube, gently swirling after each addition.

  16. Set the lab timer for 15 minutes and allow the capped WBC tube to incubate. Swirl the cell preparation several times during the incubation.

  17. With a sterile plastic syringe, add half of the saved LPP (or about 8 mL) from the LPP tube. Cap and gently swirl the contents of WBC tube to resuspend the cells.

  18. Centrifuge the WBC tube at 450 g for 5 minutes (or 150 g for 8 minutes). Decant supernatant into the wash tube leaving behind about 0.5 mL of the supernate to cover the cells.

  19. Assay the activity in the WBC tube and in the wash tube in a dose calibrator and record.

  20. With a sterile plastic syringe add the remaining LPP to the cell button and gently resuspend by swirling. With a sterile syringe fitted with a 19 gauge needle, resuspend the cells by drawing the cells up into the syringe and expressing the suspension against the tube gently once or twice. Alternatively, draw up the cells into a syringe fitted with the filtered 19 gauge needle, and replace the needle with an unfiltered 19 or 20 gauge needle.

  21. Reserve in the WBC tube a minimum amount of white cell suspension for a WBC count. A microscopic examination should also be completed to observe for clumping. Draw up the patient's dose (7.4 to 18.5 MBq, 200-500 µCi) and check the syringe in the dose calibrator. Record the measurement.


QUALITY CONTROL


It is generally advantageous to record any observations on cell abnormalities (e.g., cell clumping). A trypan blue exclusion test may also be performed.


It is recommended that the preparation be used within one hour of labeling (See Precautions).



How is Indium Oxyquinoline Supplied


Indium In 111 oxyquinoline solution is supplied in a vial as a single use only product containing 37 MBq, 1.0 mCi in 1.0 mL aqueous solution at the calibration date stated on the label. Vials are packaged in individual lead shields.


(NDC 17156-021-01)


The contents of the vial are radioactive and adequate shielding and handling precautions must be maintained.


This radiopharmaceutical is licensed by Illinois Department of Nuclear Safety for distribution to persons licensed pursuant to 32 Ill. Adm. Code 330.260 (a) and Part 335, Subpart E, 335.4010, or under equivalent licenses of an Agreement State or a Licensing State.



SPECIAL HANDLING AND STORAGE


Indium In 111 oxyquinoline solution should be stored at room temperature (15-25 °C, 59-77 °F).


Indium In 111 oxyquinoline labeled autologous leukocytes should preferably be reinjected within one hour of labeling. The labeled cells may be stored at room temperature (15-25 °C, 59-77 °F) for up to three hours following completion of the cell labeling procedure. Reinjection of indium In 111 oxyquinoline labeled autologous leukocytes more than 5 hours after initial blood drawing is not recommended.


Sterile technique must be used throughout the collection, labeling and re-injection procedures.



Amersham Health

Medi-Physics, Inc.

Arlington Heights, IL 60004

1-800-654-0118


Printed in U.S.A.


Manufactured by:

Amersham plc,

Amersham, England


43-2015J


CODE IN.15PA








INDIUM IN 111 OXYQUINOLINE 
indium in-111 oxyquinoline  solution










Product Information
Product TypeHUMAN PRESCRIPTION DRUGNDC Product Code (Source)17156-021
Route of AdministrationINTRAVENOUSDEA Schedule    











INGREDIENTS
Name (Active Moiety)TypeStrength
Indium In-111 Oxyquinoline (Indium In-111 Oxyquinoline)Active1 MICROGRAM  In 1 MILLILITER
Polysorbate 80Inactive100 MICROGRAM  In 1 MILLILITER


















Product Characteristics
Color    Score    
ShapeSize
FlavorImprint Code
Contains      














Packaging
#NDCPackage DescriptionMultilevel Packaging
117156-021-011 VIAL In 1 BOXcontains a VIAL
11 mL (MILLILITER) In 1 VIALThis package is contained within the BOX (17156-021-01)

Revised: 05/2006Amersham Health Medi Physics, Inc.

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