Sunday, February 28, 2010

Opizone




Opizone may be available in the countries listed below.


Ingredient matches for Opizone



Naltrexone

Naltrexone hydrochloride (a derivative of Naltrexone) is reported as an ingredient of Opizone in the following countries:


  • United Kingdom

International Drug Name Search

Saturday, February 27, 2010

Alomide


Alomide is a brand name of lodoxamide ophthalmic, approved by the FDA in the following formulation(s):


ALOMIDE (lodoxamide tromethamine - solution/drops; ophthalmic)



  • Manufacturer: ALCON

    Approval date: September 23, 1993

    Strength(s): EQ 0.1% BASE [RLD]

Has a generic version of Alomide been approved?


No. There is currently no therapeutically equivalent version of Alomide available.


Note: Fraudulent online pharmacies may attempt to sell an illegal generic version of Alomide. 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


Patents are granted by the U.S. Patent and Trademark Office at any time during a drug's development and may include a wide range of claims.




  • Use of lodoxamide to treat ophthalmic allergic conditions
    Patent 5,457,126
    Issued: October 10, 1995
    Inventor(s): Aoki; K. Roger & DeSantis; Louis M.
    Assignee(s): Alcon Laboratories, Inc.
    Disclosed are methods of using certain defined phenylene dioxamic acids in treating allergic ocular responses, such as, hayfever, conjunctivitis, atopic and keratoconjunctivitis, vernal conjunctivitis, giant capillary conjunctivitis and other diseases where mast cell degranulation are important in the etiology, by topical administration of said active to the affected eye; also disclosed are pharmaceutical compositions comprising said actives.
    Patent expiration dates:

    • October 10, 2012
      ✓ 
      Patent use: TREATMENT OF OCULAR ALLERGIC RESPONSE IN HUMAN EYES



See also...

  • Alomide Consumer Information (Wolters Kluwer)
  • Alomide Consumer Information (Cerner Multum)
  • Alomide Advanced Consumer Information (Micromedex)
  • Alomide AHFS DI Monographs (ASHP)
  • Lodoxamide Consumer Information (Wolters Kluwer)
  • Lodoxamide ophthalmic Consumer Information (Cerner Multum)
  • Lodoxamide Ophthalmic Advanced Consumer Information (Micromedex)
  • Lodoxamide Tromethamine AHFS DI Monographs (ASHP)

Friday, February 26, 2010

Risperdal Consta


See also: Generic Risperdal


Risperdal Consta is a brand name of risperidone, approved by the FDA in the following formulation(s):


RISPERDAL CONSTA (risperidone - injectable; intramuscular)



  • Manufacturer: JANSSEN PHARMS

    Approval date: October 29, 2003

    Strength(s): 25MG/VIAL [RLD], 37.5MG/VIAL, 50MG/VIAL


  • Manufacturer: JANSSEN PHARMS

    Approval date: April 12, 2007

    Strength(s): 12.5MG/VIAL

Has a generic version of Risperdal Consta been approved?


No. There is currently no therapeutically equivalent version of Risperdal Consta available.


Note: Fraudulent online pharmacies may attempt to sell an illegal generic version of Risperdal Consta. 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


Patents are granted by the U.S. Patent and Trademark Office at any time during a drug's development and may include a wide range of claims.




  • Method of inhibiting neurotransmitter activity using microencapsulated 3-piperidiny2-substituted 1,2-benzisoxazoles and 1,2-benzisothiazoles
    Patent 5,688,801
    Issued: November 18, 1997
    Inventor(s): Mesens; Jean & Rickey; Michael E. & Atkins; Thomas J.
    Assignee(s): Janssen Pharmaceutica
    Alkermes Controlled Therapeutics Inc. II
    A pharmaceutical composition comprising a biodegradable and biocompatible composition comprising a 1,2 benzazole within a polymeric matrix. The 1,2 benzazole composition, pharmaceutically acceptable acid addition salts thereof, are potent antagonists of a series of neurotransmitters, particularly serotonin and dopamine. A method of inhibiting both serotonergic overactivity and dopaminergic overstimulation in animals is provided by administration of a biodegradable and biocompatible microparticle composition comprising a 1,2 benzazole or a pharmaceutically acceptable acid addition salt thereof. A method of treating warm blooded animals suffering from psychotic disorders, and a method of preparing the biodegradable and biocompatible composition are also described.
    Patent expiration dates:

    • November 18, 2014
      ✓ 
      Patent use: TREATMENT OF SCHIZOPHRENIA


    • November 18, 2014
      ✓ 
      Patent use: MONOTHERAPY OR AS ADJUNCTIVE THERAPY TO LITHIUM OR VALPROATE FOR THE MAINTENANCE TREATMENT OF BIPOLAR I DISORDER


    • May 18, 2015
      ✓ 
      Pediatric exclusivity




  • Preparation of extended shelf-life biodegradable, biocompatible microparticles containing a biologically active agent
    Patent 5,792,477
    Issued: August 11, 1998
    Inventor(s): Rickey; Michael E. & Ramstack; J. Michael & Lewis; Danny H. & Mesens; Jean
    Assignee(s): Alkermes Controlled Therapeutics, Inc. II
    Janssen Pharmaceutica
    A method for preparing biodegradable, biocompatible microparticles. A first phase is prepared that includes a biodegradable, biocompatible polymeric encapsulating binder, and an active agent having limited water solubility dissolved or dispersed in a solvent. An aqueous second phase is prepared. The first and second phases are combined to form an emulsion in which the first phase is discontinuous and the second phase is continuous. The two phases are separated. The discontinuous first phase is washed with water, or an aqueous solution of water and a solvent for residual solvent in the first phase, to reduce the level of residual solvent in the microparticles to less than about 2% by weight of the microparticles. Also disclosed are a microencapsulated drug prepared by the method for preparing biodegradable, biocompatible microparticles, and a pharmaceutical composition that includes biodegradable and biocompatible microparticles in a pharmaceutically acceptable carrier.
    Patent expiration dates:

    • May 2, 2017
      ✓ 
      Drug product


    • November 2, 2017
      ✓ 
      Pediatric exclusivity




  • Preparation of biodegradable, biocompatible microparticles containing a biologically active agent
    Patent 5,916,598
    Issued: June 29, 1999
    Inventor(s): Rickey; Michael E. & Ramstack; J. Michael & Lewis; Danny H.
    Assignee(s): Alkermes Controlled Therapeutics Inc. II
    A method for preparing biodegradable, biocompatible microparticles. A first phase is prepared that includes a biodegradable, biocompatible polymer, an active agent, and a solvent. An immiscible second phase is prepared. The first and second phases are combined to form an emulsion in which the first phase is discontinuous and the second phase is continuous. The two phases are immersed in a quench liquid that includes a quench medium and a quantity of the solvent. The quantity of the solvent is selected to control a rate of extraction of the solvent from the first phase. The first phase is isolated in the form of microparticles. Also disclosed is a microencapsulated active agent prepared by the method for preparing biodegradable, biocompatible microparticles.
    Patent expiration dates:

    • May 2, 2017
      ✓ 
      Drug product


    • November 2, 2017
      ✓ 
      Pediatric exclusivity




  • Microencapsulated 3-piperidinyl-substituted 1,2-benzisoxazoles and 1,2-benzisothiazoles
    Patent 5,965,168
    Issued: October 12, 1999
    Inventor(s): Mesens; Jean & Rickey; Michael E. & Atkins; Thomas J.
    Assignee(s): Alkermes Controlled Therapeutics, Inc. II
    Janssen Pharmaceutica
    The invention relates to a pharmaceutical composition comprising a biodegradable and biocompatible microparticle composition comprising a 1,2-benzazole of the formula ##STR1## and the pharmaceutically acceptable acid addition salts thereof, within a polymeric matrix.
    Patent expiration dates:

    • November 19, 2013
      ✓ 
      Drug product


    • May 19, 2014
      ✓ 
      Pediatric exclusivity




  • Preparation of biodegradable, biocompatible microparticles containing a biologically active agent
    Patent 6,110,503
    Issued: August 29, 2000
    Inventor(s): Rickey; Michael E. & Ramstack; J. Michael & Lewis; Danny H.
    Assignee(s): Alkermes Controlled Therapeutics Inc.
    A method for preparing biodegradable, biocompatible microparticles. A first phase is prepared that includes a biodegradable, biocompatible polymer, an active agent, and a solvent. An immiscible second phase is prepared. The first and second phases are combined to form an emulsion in which the first phase is discontinuous and the second phase is continuous. The two phases are immersed in a quench liquid that includes a quench medium and a quantity of the solvent. The quantity of the solvent is selected to control a rate of extraction of the solvent from the first phase. The first phase is isolated in the form of microparticles. Also disclosed is a microencapsulated active agent prepared by the method for preparing biodegradable, biocompatible microparticles.
    Patent expiration dates:

    • May 2, 2017
      ✓ 
      Drug product


    • November 2, 2017
      ✓ 
      Pediatric exclusivity




  • Microencapsulated 3-piperidinyl-substituted 1,2-benzisoxazoles and 1,2-benzisothiazoles
    Patent 6,110,921
    Issued: August 29, 2000
    Inventor(s): Mesens; Jean & Rickey; Michael E. & Atkins; Thomas J.
    Assignee(s): Alkermes Controlled Therapeutics Inc. II
    Janssen Pharmaceutica
    The invention relates to a method of treating psychotic disorders comprising a biodegradable and biocompatible microparticle composition comprising a 1,2-benzazole of the formula ##STR1## and the pharmaceutically acceptable acid addition salts thereof.
    Patent expiration dates:

    • November 19, 2013
      ✓ 
      Patent use: TREATMENT OF SCHIZOPHRENIA


    • May 19, 2014
      ✓ 
      Pediatric exclusivity




  • Preparation of microparticles having a selected release profile
    Patent 6,194,006
    Issued: February 27, 2001
    Inventor(s): Lyons; Shawn L. & Ramstack; J. Michael & Wright; Steven G.
    Assignee(s): Alkermes Controlled Therapeutics Inc. II
    An improved method for preparing microparticles that exhibit controlled release of an effective amount of an active agent over an extended period of time. More particularly, a method is provided for preparing microparticles having a selected release profile for release of active agent contained in the microparticles. By adjusting the degree of drying that is performed during the preparation of the microparticles, the release profile can be controlled. By performing no intermediate drying, an initial burst and a substantially linear release profile is achieved. By performing substantially complete intermediate drying, an initial lag phase and a substantially sigmoidal release profile is achieved.
    Patent expiration dates:

    • December 30, 2018
      ✓ 
      Drug product


    • June 30, 2019
      ✓ 
      Pediatric exclusivity




  • Microencapsulated 3-piperidinyl-substituted 1,2-benzisoxazoles and 1,2-benzisothiazoles
    Patent 6,368,632
    Issued: April 9, 2002
    Inventor(s): Jean; Mesens & Michael E.; Rickey & Thomas J.; Atkins
    Assignee(s): Janssen Pharmaceutica
    Alkermes Controlled Therapeutics Inc. II
    Method of treating warm blooded animals suffering from psychotic disorders. The method includes administering a pharmaceutically effective amount of sustained-release microparticles that include risperidone, or a pharmaceutically acceptable acid addition salt thereof, and a biodegradable and biocompatible polymeric matrix.
    Patent expiration dates:

    • November 19, 2013
      ✓ 
      Patent use: TREATMENT OF SCHIZOPHRENIA


    • May 19, 2014
      ✓ 
      Pediatric exclusivity




  • Preparation of microparticles having a selected release profile
    Patent 6,379,703
    Issued: April 30, 2002
    Inventor(s): Shawn L.; Lyons & J. Michael; Ramstack & Steven G.; Wright
    Assignee(s): Alkermes Controlled Therapeutics Inc., II
    An improved method for preparing microparticles that exhibit controlled release of an effective amount of an active agent over an extended period of time. More particularly, a method is provided for preparing microparticles having a selected release profile for release of active agent contained in the microparticles. By adjusting the degree of drying that is performed during the preparation of the microparticles, the release profile can be controlled. By performing no intermediate drying, an initial burst and a substantially linear release profile is achieved. By performing substantially complete intermediate drying, an initial lag phase and a substantially sigmoidal release profile is achieved.
    Patent expiration dates:

    • December 30, 2018
      ✓ 
      Drug product


    • June 30, 2019
      ✓ 
      Pediatric exclusivity




  • Preparation of biodegradable, biocompatible microparticles containing a biologically active agent
    Patent 6,403,114
    Issued: June 11, 2002
    Inventor(s): Michael E.; Rickey & J. Michael; Ramstack & Danny H.; Lewis
    Assignee(s): Alkermes Controlled Therapeutics Inc. II
    A method for preparing biodegradable, biocompatible microparticles. A first phase is prepared that includes a biodegradable, biocompatible polymer, an active agent, and a solvent. A second phase is prepared. The first and second phases are combined to form an emulsion in which the first phase is discontinuous and the second phase is continuous. The discontinuous first phase is separated from the continuous second phase. The residual level of solvent in the discontinuous first phase is reduced to less than about 2% by weight.
    Patent expiration dates:

    • May 2, 2017
      ✓ 
      Drug product


    • November 2, 2017
      ✓ 
      Pediatric exclusivity




  • Preparation of microparticles having a selected release profile
    Patent 6,596,316
    Issued: July 22, 2003
    Inventor(s): Shawn L.; Lyons & J. Michael; Ramstack & Steven G.; Wright
    Assignee(s): Alkermes Controlled Therapeutics, Inc. II
    An improved method for preparing microparticles that exhibit controlled release of an effective amount of an active agent over an extended period of time. More particularly, a method is provided for preparing microparticles having a selected release profile for release of active agent contained in the microparticles. By adjusting the degree of drying that is performed during the preparation of the microparticles, the release profile can be controlled. By performing no intermediate drying, an initial burst and a substantially linear release profile is achieved. By performing substantially complete intermediate drying, an initial lag phase and a substantially sigmoidal release profile is achieved.
    Patent expiration dates:

    • December 30, 2018
      ✓ 
      Drug product


    • June 30, 2019
      ✓ 
      Pediatric exclusivity




  • Preparation of injectable suspensions having improved injectability
    Patent 6,667,061
    Issued: December 23, 2003
    Inventor(s): J. Michael; Ramstack & M. Gary I.; Riley & Stephen E.; Zale & Joyce M.; Hotz & Olufunmi L.; Johnson
    Assignee(s): Alkermes Controlled Therapeutics, Inc.
    Injectable compositions having improved injectability. The injectable compositions include microparticles suspended in an aqueous injection vehicle having a viscosity of at least 20 cp at 20° C. The increased viscosity of the injection vehicle that constitutes the fluid phase of the suspension significantly reduces in vivo injectability failures. The injectable compositions can be made by mixing dry microparticles with an aqueous injection vehicle to form a suspension, and then mixing the suspension with a viscosity enhancing agent to increase the viscosity of the fluid phase of the suspension to the desired level for improved injectability.
    Patent expiration dates:

    • May 25, 2020
      ✓ 
      Drug product


    • November 25, 2020
      ✓ 
      Pediatric exclusivity




  • Microencapsulated 3-piperidinyl-substituted 1,2-benzisoxazoles and 1,2-benzisothiazoles
    Patent 7,547,452
    Issued: June 16, 2009
    Inventor(s): Atkins; Thomas J. & Rickey; Michael E. & Mesens; Jean
    Assignee(s): Alkermes, Inc.
    Janssen Pharmaceutica, N.V
    Sustained-release microparticle composition. The microparticle composition can be formulated to provide extended release over a period of from about 7 days to about 200 days. The microparticles may be formulated with a biodegradable and biocompatible polymer, and an active agent, such as risperidone, 9-hydroxy-risperidone, and pharmaceutically acceptable acid addition salts of the foregoing.
    Patent expiration dates:

    • November 19, 2013
      ✓ 
      Drug product


    • May 19, 2014
      ✓ 
      Pediatric exclusivity



Related Exclusivities

Exclusivity is exclusive marketing rights granted by the FDA upon approval of a drug and can run concurrently with a patent or not. Exclusivity is a statutory provision and is granted to an NDA applicant if statutory requirements are met.

  • Exclusivity expiration dates:
    • May 15, 2012 - USE AS ADJUNCTIVE THERAPY WITH LITHIUM OR VALPROATE FOR THE MAINTENANCE TREATMENT OF BIPOLAR I DISORDER

    • May 15, 2012 - MONOTHERAPY FOR THE MAINTENANCE TREATMENT OF BIPOLAR I DISORDER

See also...

  • Risperdal Consta Consumer Information (Drugs.com)
  • Risperdal Consta Consumer Information (Wolters Kluwer)
  • Risperdal Consta Advanced Consumer Information (Micromedex)
  • Risperidone Consumer Information (Drugs.com)
  • Risperidone Consumer Information (Wolters Kluwer)
  • Risperidone Orally Disintegrating Tablets Consumer Information (Wolters Kluwer)
  • Risperidone Solution Consumer Information (Wolters Kluwer)
  • Risperidone Tablets Consumer Information (Wolters Kluwer)
  • Risperidone Consumer Information (Cerner Multum)
  • Risperidone Advanced Consumer Information (Micromedex)
  • Risperidone Intramuscular Advanced Consumer Information (Micromedex)
  • Risperidone AHFS DI Monographs (ASHP)

Friday, February 19, 2010

desmopressin nasal



Generic Name: desmopressin (nasal) (DEZ mo press in)

Brand Names: DDAVP Nasal, DDAVP Rhinal Tube, Stimate


What is desmopressin nasal?

Desmopressin is a man-made form of a hormone that occurs naturally in the pituitary gland. This hormone is important for many functions including blood flow, blood pressure, kidney function, and regulating how the body uses water.


Desmopressin nasal is used to treat central cranial diabetes insipidus, and increased thirst and urination caused by head surgery or head trauma.


Desmopressin nasal is also used to treat hemophilia A or von Willebrand's disease Type I.


Desmopressin nasal may also be used for other purposes not listed in this medication guide.


What is the most important information I should know about desmopressin nasal?


It is very important to reduce your intake of water and other fluids while you are using desmopressin. Drinking too much water can cause your body to lose sodium, which may lead to a serious, life-threatening electrolyte imbalance.

Fluid restriction is especially important in children and older adults using desmopressin nasal. Follow your doctor's instructions about the type and amount of liquids you should drink.


You should not use this medication if you have severe kidney disease or if you have ever had hyponatremia (low sodium levels in your body).

Before using desmopressin nasal, tell your doctor if you have heart disease, coronary artery disease, congestive heart failure, kidney disease, cystic fibrosis, high or low blood pressure, an electrolyte imbalance, or a psychological disorder that causes extreme or unusual thirst.


Desmopressin nasal may be less effective if you have any swelling or scarring inside your nose, or any nasal or sinus problems (such as deviated septum).


This medication comes with patient instructions for safe and effective use. Follow these directions carefully. Ask your doctor or pharmacist if you have any questions.


To be sure desmopressin nasal is helping your condition, your blood will need to be tested often. This will help your doctor determine how long to treat you with this medication. Do not miss any scheduled appointments.


What should I discuss with my healthcare provider before using desmopressin nasal?


You should not use this medication if you are allergic to desmopressin, or if you have:

  • severe kidney disease; or




  • if you have ever had hyponatremia (low sodium levels in your body).



Before using desmopressin nasal, tell your doctor if you are allergic to any medications, or if you have:



  • heart disease, coronary artery disease;




  • congestive heart failure;




  • kidney disease;




  • cystic fibrosis;




  • high or low blood pressure;




  • an electrolyte imbalance; or




  • a psychologic disorder that causes extreme or unusual thirst.



If you have any of these conditions, you may need a dose adjustment or special tests to safely use desmopressin.


Desmopressin nasal may be less effective if you have any swelling or scarring inside your nose, or any nasal or sinus problems (such as deviated septum).


FDA pregnancy category B. This medication is not expected to harm an unborn baby. Do not use desmopressin nasal without telling your doctor if you are pregnant. It is not known whether desmopressin nasal passes into breast milk, or if it could harm a nursing baby. Do not use desmopressin nasal without telling your doctor if you are breast-feeding a baby.

How should I use desmopressin nasal?


Use this medication exactly as prescribed by your doctor. Do not use it in larger amounts or for longer than recommended. Follow the directions on your prescription label.


This medication comes with patient instructions for safe and effective use. Follow these directions carefully. Ask your doctor or pharmacist if you have any questions.


It is very important to reduce your intake of water and other fluids while you are using desmopressin. Drinking too much water can cause your body to lose sodium, which may lead to a serious, life-threatening electrolyte imbalance.

Fluid restriction is especially important in children and older adults using desmopressin nasal. Follow your doctor's instructions about the type and amount of liquids you should drink.


Before using desmopressin nasal spray for the first time, prime the spray pump by pressing down on the pump 4 times.


To be sure this medication is helping your condition, your blood will need to be tested often. This will help your doctor determine how long to treat you with desmopressin nasal. Do not miss any scheduled appointments.


Keep track of how many sprays have been used from each bottle of desmopressin nasal spray. Stimate nasal spray contains enough desmopressin for the priming spray plus 25 full sprays. DDAVP nasal spray contains enough desmopressin for the priming spray plus 50 sprays. Your patient instructions may include a check-off chart to help you keep an accurate record or sprays you use. If you are treating hemophilia or von Willebrand's disease, call your doctor if your bleeding is not controlled during treatment with desmopressin nasal.

The desmopressin nasal spray bottle should be thrown away after the specified number of sprays have been used, even if there is medicine leftover in the bottle. Do not try to pour solution from one bottle to another.


Store DDAVP nasal spray at room temperature away from moisture and heat. Keep the bottle in an upright position when not in use. Store Stimate nasal spray or DDAVP Rhinal Tube in the refrigerator. Do not freeze. If refrigeration is not available, you may keep the closed bottles at room temperature for up to 3 weeks.

What happens if I miss a dose?


Use the missed dose as soon as you remember. If it is almost time for your next dose, wait until then to use the medicine and skip the missed dose. Do not use extra medicine to make up the missed dose.


What happens if I overdose?


Seek emergency medical attention if you think you have used too much of this medicine.

Overdose symptoms may include headache, confusion, drowsiness, rapid weight gain, or urination problems.


What should I avoid while using desmopressin nasal?


Follow your doctor's instructions about any restrictions on food, beverages, or activity while you are using desmopressin.


Desmopressin nasal side effects


Get emergency medical help if you have any of these signs of an allergic reaction: hives; difficulty breathing; swelling of your face, lips, tongue, or throat. Stop using desmopressin nasal and call your doctor at once if you have any of these serious side effects:

  • nausea, vomiting, weakness, loss of appetite, headache, feeling restless or irritable, confusion, hallucinations, muscle pain or weakness, and/or seizure;




  • feeling like you might pass out;




  • swelling;




  • chest pain, fast or pounding heart rate;




  • vaginal pain;




  • nosebleed; or




  • dangerously high blood pressure (severe headache, blurred vision, buzzing in your ears, anxiety, confusion, chest pain, shortness of breath, uneven heartbeats, seizure).



Less serious side effects may include:



  • runny or stuffy nose;




  • sore throat, cough, or other cold symptoms;




  • eye redness or watering;




  • eye itching or increased sensitivity to light;




  • headache, weakness;




  • feeling dizzy or agitated;




  • nausea, vomiting, stomach pain;




  • hot or cold feeling; or




  • warmth, redness, or tingly feeling in your face.



This is not a complete list of side effects and others may occur. Tell your doctor about any unusual or bothersome side effect. You may report side effects to FDA at 1-800-FDA-1088.


Desmopressin Dosing Information


Usual Adult Dose for Diabetes Insipidus:

Initial dose: 0.05 mg orally twice a day or
1 to 2 mcg IV twice a day or
1 to 2 mcg subcutaneously twice a day or
5 to 40 mcg spray intranasally twice a day or
0.1 to 0.4 mL via rhinal tube intranasally twice a day.
The optimal dosage depends on the patient's response (duration of sleep and adequate, not excessive water turnover). The morning and evening doses should be separately adjusted for an adequate diurnal rhythm of water turnover.

Usual Adult Dose for Hemophilia A:

IV: 0.3 mcg/kg once slowly over 15-30 minutes. Preoperative IV doses may be given 30 minutes prior to scheduled procedure. Blood pressure and heart rate monitoring during infusion is recommended. Repeat administration should be determined by laboratory response as well as the clinical condition of the patient.
Intranasal: 1 spray (1.5 mg/mL) in each nostril one time.
Demonstration of an adequate improvement in coagulation profile after administration is recommended prior to any surgical procedures. Preoperative doses may be given 2 hours prior to the scheduled procedure. Repeat administration should be determined by laboratory response and clinical condition of the patient.

Usual Adult Dose for von Willebrand's Disease:

IV: 0.3 mcg/kg once slowly over 15-30 minutes. Preoperative IV doses may be given 30 minutes prior to scheduled procedure. Blood pressure and heart rate monitoring during infusion is recommended. Repeat administration should be determined by laboratory response as well as the clinical condition of the patient.
Intranasal: 1 spray (1.5 mg/mL) in each nostril one time.
Demonstration of an adequate improvement in coagulation profile after administration is recommended prior to any surgical procedures. Preoperative doses may be given 2 hours prior to the scheduled procedure. Repeat administration should be determined by laboratory response and clinical condition of the patient. The nasal spray should not be used to treat patients with type IIB von Willebrand's disease since platelet aggregation may be induced.

Usual Adult Dose for Primary Nocturnal Enuresis:

Oral: 0.2 to 0.6 mg once before bedtime.

Usual Pediatric Dose for Diabetes Insipidus:

Infants 3 months of age to children 12 years of age:
Intranasal: 5 mcg/day as a single dose or in 2 divided doses. Dose range is 5 to 30 mcg/day. The morning and evening doses should be separately adjusted for an adequate diurnal rhythm of water turnover.
Oral: 0.05 mg twice a day. Dose range is 0.1 to 0.8 mg daily.
IV and subcutaneously: No definitive dosing available. Adult dosing should not be used in this age group; adverse events such as hyponatremia-induced seizures may occur. Dose should be reduced. Some have suggested an initial dosage range of 0.1 to 1 mcg in 1 or 2 divided doses. Initiate at low dose and increase as necessary. Closely monitor serum sodium levels and urine output; fluid restriction is recommended.

Children more than 12 years of age:
Intranasal: 5 to 40 mcg/day divided into 1 to 3 doses. The morning and evening doses should be separately adjusted for an adequate diurnal rhythm of water turnover.
Oral: 0.05 mg twice daily. Dose range is 0.1 to 1.2 mg divided into 2 or 3 doses.
IV: 1 to 2 mcg twice a day
Subcutaneously: 1 to 2 mcg twice a day

Use in children requires careful fluid intake restrictions to prevent possible hyponatremia and water intoxication. The optimal dosage depends on the patient's response (duration of sleep and adequate, not excessive water turnover).

Usual Pediatric Dose for Hemophilia A:

Infants 3 months of age and children:
IV: 0.3 mcg/kg by slow infusion over 15-30 minutes beginning 30 minutes before procedure. May repeat dose if needed.

Children more than 12 years of age:
IV: 0.3 mcg/kg once slowly over 15-30 minutes.
Intranasal:
50 kg or less: 150 mcg
more than 50 kg: 150 mcg in each nostril.
Demonstration of an adequate improvement in coagulation profile after administration is recommended prior to any surgical procedures. Preoperative doses may be given 2 hours prior to the scheduled procedure. Repeat administration should be determined by laboratory response and clinical condition of the patient.

Usual Pediatric Dose for von Willebrand's Disease:

Infants 3 months of age and children:
IV: 0.3 mcg/kg by slow infusion over 15 to 30 minutes beginning 30 minutes before procedure. May repeat dose if needed.

Children more than 12 years of age:
IV: 0.3 mcg/kg once slowly over 15 to 30 minutes.
Intranasal:
50 kg or less: 150 mcg
More than 50 kg: 150 mcg in each nostril.
Demonstration of an adequate improvement in coagulation profile after administration is recommended prior to any surgical procedures. Preoperative doses may be given 2 hours prior to the scheduled procedure. Repeat administration should be determined by laboratory response and clinical condition of the patient. The nasal spray should not be used to treat patients with type IIB von Willebrand's disease since platelet aggregation may be induced.

Usual Pediatric Dose for Primary Nocturnal Enuresis:

6 years or older:
0.2 to 0.6 mg orally once daily before bedtime.


What other drugs will affect desmopressin nasal?


Many drugs can interact with desmopressin nasal. Below is just a partial list. Tell your doctor if you are using:



  • carbamazepine (Carbatrol, Tegretol);




  • chlorpromazine (Thorazine);




  • lamotrigine (Lamictal);




  • oxybutynin (Ditropan, Urotrol, Oxytrol);




  • vasopressin (Pitressin);




  • a narcotic pain medicine such as fentanyl (Actiq, Duragesic), hydrocodone (Lortab, Vicodin), oxycodone (Oxycontin), and others;




  • an "SSRI" antidepressant such as citalopram (Celexa), escitalopram (Lexapro), fluoxetine (Prozac, Sarafem), fluvoxamine (Luvox), paroxetine (Paxil), or sertraline (Zoloft);




  • a tricyclic antidepressant such as amitriptyline (Elavil, Etrafon), clomipramine (Anafranil), desipramine (Norpramin), doxepin (Sinequan), imipramine (Janimine, Tofranil), and others;




  • medicine to treat erectile dysfunction, such as sildenafil (Viagra), tadalafil (Cialis), or vardenafil (Levitra);




  • drugs to treat high blood pressure or a prostate disorder, such as alfuzosin (Uroxatral), doxazosin (Cardura), prazosin (Minipress), terazosin (Hytrin), tamsulosin (Flomax);




  • a beta-blocker such as atenolol (Tenormin), bisoprolol (Zebeta, Ziac), labetalol (Normodyne, Trandate), metoprolol (Lopressor, Toprol), nadolol (Corgard), propranolol (Inderal, InnoPran), sotalol (Betapace), or timolol (Blocadren); or




  • an NSAID (non-steroidal anti-inflammatory drug) such as ibuprofen (Motrin, Advil), naproxen (Aleve, Naprosyn), diclofenac (Cataflam, Voltaren), etodolac (Lodine), indomethacin (Indocin), and others.



This list is not complete and there may be other drugs that can interact with desmopressin nasal. Tell your doctor about all your prescription and over-the-counter medications, vitamins, minerals, herbal products, and drugs prescribed by other doctors. Do not start a new medication without telling your doctor.



More desmopressin resources


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


Compare desmopressin with other medications


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  • von Willebrand's Disease


Where can I get more information?


  • Your pharmacist can provide more information about desmopressin nasal.

See also: desmopressin side effects (in more detail)


Thursday, February 18, 2010

Minims Proxymetacaine




Minims Proxymetacaine may be available in the countries listed below.


In some countries, this medicine may only be approved for veterinary use.

UK matches:

  • Minims Proxymetacaine and Fluorescein
  • Minims Proxymetacaine Hydrochloride 0.5% w/v (SPC)
  • Minims Proxymetacaine hydrochloride 0.5% w/v & Fluorescein sodium 0.25% w/v (SPC)

Ingredient matches for Minims Proxymetacaine



Proxymetacaine

Proxymetacaine hydrochloride (a derivative of Proxymetacaine) is reported as an ingredient of Minims Proxymetacaine in the following countries:


  • South Africa

  • United Kingdom

Tetracaine

Tetracaine hydrochloride (a derivative of Tetracaine) is reported as an ingredient of Minims Proxymetacaine in the following countries:


  • South Africa

International Drug Name Search

Glossary

SPC Summary of Product Characteristics (UK)

Click for further information on drug naming conventions and International Nonproprietary Names.

Wednesday, February 17, 2010

Maxitrol


Maxitrol is a brand name of dexamethasone/neomycin/polymyxin b ophthalmic, approved by the FDA in the following formulation(s):


MAXITROL (dexamethasone; neomycin sulfate; polymyxin b sulfate - ointment; ophthalmic)



  • Manufacturer: FALCON PHARMS

    Approved Prior to Jan 1, 1982

    Strength(s): 0.1%;EQ 3.5MG BASE/GM;10,000 UNITS/GM [RLD][AT]

MAXITROL (dexamethasone; neomycin sulfate; polymyxin b sulfate - suspension/drops; ophthalmic)



  • Manufacturer: FALCON PHARMS

    Approved Prior to Jan 1, 1982

    Strength(s): 0.1%;EQ 3.5MG BASE/ML;10,000 UNITS/ML [RLD][AT]

Has a generic version of Maxitrol been approved?


Yes. The following products are equivalent to Maxitrol:


DEXASPORIN (dexamethasone; neomycin sulfate; polymyxin b sulfate suspension/drops; ophthalmic)



  • Manufacturer: BAUSCH AND LOMB

    Approval date: September 13, 1995

    Strength(s): 0.1%;EQ 3.5MG BASE/ML;10,000 UNITS/ML [AT]

MAXITROL (dexamethasone; neomycin sulfate; polymyxin b sulfate suspension/drops; ophthalmic)



  • Manufacturer: ALCON

    Approval date: May 22, 1984

    Strength(s): 0.1%;EQ 3.5MG BASE/ML;10,000 UNITS/ML [AT]

NEOMYCIN AND POLYMYXIN B SULFATES AND DEXAMETHASONE (dexamethasone; neomycin sulfate; polymyxin b sulfate ointment; ophthalmic)



  • Manufacturer: BAUSCH AND LOMB

    Approval date: July 25, 1994

    Strength(s): 0.1%;EQ 3.5MG BASE/GM;10,000 UNITS/GM [AT]


  • Manufacturer: FERA PHARMS

    Approval date: July 31, 1989

    Strength(s): 0.1%;EQ 3.5MG BASE/GM;10,000 UNITS/GM [AT]

NEOMYCIN AND POLYMYXIN B SULFATES AND DEXAMETHASONE (dexamethasone; neomycin sulfate; polymyxin b sulfate suspension/drops; ophthalmic)



  • Manufacturer: ALCON UNIVERSAL

    Approval date: November 17, 1986

    Strength(s): 0.1%;EQ 3.5MG BASE/ML;10,000 UNITS/ML [AT]

Note: Fraudulent online pharmacies may attempt to sell an illegal generic version of Maxitrol. 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 Maxitrol.

See also...

  • Maxitrol Drops Consumer Information (Wolters Kluwer)
  • Maxitrol Ointment Consumer Information (Wolters Kluwer)
  • Maxitrol Consumer Information (Cerner Multum)
  • Dexamethasone/Neomycin/Polymyxin B Drops Consumer Information (Wolters Kluwer)
  • Dexamethasone/Neomycin/Polymyxin B Ointment Consumer Information (Wolters Kluwer)
  • Neomycin, polymyxin B, and dexamethasone ophthalmic Consumer Information (Cerner Multum)

Saturday, February 6, 2010

Meiclox




Meiclox may be available in the countries listed below.


Ingredient matches for Meiclox



Cloxacillin

Cloxacillin sodium salt (a derivative of Cloxacillin) is reported as an ingredient of Meiclox in the following countries:


  • Thailand

International Drug Name Search

Kamelyn




Kamelyn may be available in the countries listed below.


Ingredient matches for Kamelyn



Betamethasone

Betamethasone 17α-valerate (a derivative of Betamethasone) is reported as an ingredient of Kamelyn in the following countries:


  • Italy

Gentamicin

Gentamicin sulfate (a derivative of Gentamicin) is reported as an ingredient of Kamelyn in the following countries:


  • Italy

International Drug Name Search

Thursday, February 4, 2010

Ospen




Ospen may be available in the countries listed below.


Ingredient matches for Ospen



Phenoxymethylpenicillin

Phenoxymethylpenicillin is reported as an ingredient of Ospen in the following countries:


  • Austria

  • Bahrain

  • Bosnia & Herzegowina

  • Costa Rica

  • Cyprus

  • Dominican Republic

  • El Salvador

  • Georgia

  • Greece

  • Guatemala

  • Indonesia

  • Jordan

  • Kuwait

  • Latvia

  • Lebanon

  • Lithuania

  • Nicaragua

  • Oman

  • Panama

  • Qatar

  • Romania

  • Saudi Arabia

  • Singapore

  • Slovenia

  • Sudan

  • Tunisia

  • United Arab Emirates

  • Yemen

Phenoxymethylpenicillin benzathine (a derivative of Phenoxymethylpenicillin) is reported as an ingredient of Ospen in the following countries:


  • Austria

  • Bosnia & Herzegowina

  • Czech Republic

  • Estonia

  • Hungary

  • Poland

  • Russian Federation

  • Slovakia

  • Slovenia

  • Switzerland

Phenoxymethylpenicillin potassium (a derivative of Phenoxymethylpenicillin) is reported as an ingredient of Ospen in the following countries:


  • Czech Republic

  • Hungary

  • Poland

  • Romania

  • Slovakia

  • Switzerland

International Drug Name Search

Monday, February 1, 2010

Tetrazep-CT




Tetrazep-CT may be available in the countries listed below.


Ingredient matches for Tetrazep-CT



Tetrazepam

Tetrazepam is reported as an ingredient of Tetrazep-CT in the following countries:


  • Germany

International Drug Name Search