Nilutamide

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(Redirected from Anandrone)

What is Nilutamide?[edit | edit source]

  • Nilutamide (Nilandron) is an oral nonsteroidal antiandrogen similar in structure to flutamide that is used widely in the therapy of prostate cancer.
Nilutamide
Nilutamide molecule ball
Nilutamide Structure



What are the uses of this medicine?[edit | edit source]

Nilutamide (Nilandron) is used to treat:


How does this medicine work?[edit | edit source]


Who Should Not Use this medicine ?[edit | edit source]

This medicine cannot be used in patients:

  • with severe hepatic impairment
  • with severe respiratory insufficiency
  • with hypersensitivity to nilutamide or any component of this preparation


What drug interactions can this medicine cause?[edit | edit source]

  • Tell your healthcare provider about all the medicines you take, including prescription and over-the-counter medicines, vitamins and herbal supplements.
  • Be sure to mention any of the following:
  • anticoagulants ('blood thinners') such as warfarin (Coumadin), phenytoin (Dilantin), and theophylline (Theo-Dur, Slo-Phyllin, others)


Is this medicine FDA approved?[edit | edit source]

  • Nilutamide was approved for use in the United States in 1996.


How should this medicine be used?[edit | edit source]

Recommended dosage:

  • The recommended dosage is 300 mg once a day for 30 days, followed thereafter by 150 mg once a day.

Administration:

  • Nilutamide comes as a tablet to take by mouth.
  • It is usually taken with or without food once daily.
  • Take nilutamide at around the same time every day.


What are the dosage forms and brand names of this medicine?[edit | edit source]

This medicine is available in fallowing doasage form:

  • As Nilutamide Tablet contains 150 mg of nilutamide

This medicine is available in fallowing brand namesː

  • Nilandron


What side effects can this medication cause?[edit | edit source]

The most common side effects of this medicine include:


What special precautions should I follow?[edit | edit source]

  • Interstitial pneumonitis has been reported in patients exposed to nilutamide. If symptoms occur, Nilutamide Tablets should be immediately discontinued until it can be determined if the symptoms are drug related.
  • Rare cases of death or hospitalization due to severe liver injury have been reported post-marketing in association with the use of Nilutamide Tablets. If at any time, a patient has jaundice, or their ALT rises above 2 times the upper limit of normal, Nilutamide Tablets should be immediately discontinued with close follow-up of liver function tests until resolution.
  • Patients should be informed that Nilutamide Tablets should be started on the day of, or on the day after, surgical castration. They should also be informed that they should not interrupt their dosing of Nilutamide Tablets or stop taking this medication without consulting their physician.
  • Because of the possibility of an intolerance to alcohol (facial flushes, malaise, hypotension) following ingestion of Nilutamide Tablets, it is recommended that intake of alcoholic beverages be avoided by patients who experience this reaction.
  • Patients receiving Nilutamide Tablets reported a delay in adaptation to dark, ranging from seconds to a few minutes, when passing from a lighted area to a dark area. Patients who experience this effect should be cautioned about driving at night or through tunnels. This effect can be alleviated by the wearing of tinted glasses.


What to do in case of emergency/overdose?[edit | edit source]

Symptoms of overdosage may include:

Management of overdosage:

  • Since nilutamide is protein bound, dialysis may not be useful as treatment for overdose.
  • General supportive care, including frequent monitoring of the vital signs and close observation of the patient, is indicated.


Can this medicine be used in pregnancy?[edit | edit source]

  • It is also not known whether nilutamide can cause fetal harm when administered to a pregnant woman or can affect reproductive capacity.
  • Nilutamide should be given to a pregnant woman only if clearly needed.


Can this medicine be used in children?[edit | edit source]

  • Safety and effectiveness in pediatric patients have not been determined.


What are the active and inactive ingredients in this medicine?[edit | edit source]

Active Ingredient:

  • NILUTAMIDE

Inactive Ingredients:

  • STARCH, CORN
  • LACTOSE MONOHYDRATE
  • POVIDONE K30
  • DOCUSATE SODIUM
  • TALC
  • CALCIUM STEARATE


Who manufactures and distributes this medicine?[edit | edit source]

Manufactured by:


What should I know about storage and disposal of this medication?[edit | edit source]

  • Store at 25°C (77°F); excursions permitted between 15 to 30°C (59 to 86°F).
  • Protect from light.
  • Keep out of reach of children.


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