Saturday 31 October 2009

RE Iron Tablets





Dosage Form: tablet
RE Iron Tablets 90 mg

Indications and Usage for RE Iron Tablets


RE Iron Tablets 90mg is indicated for the prevention and treatment of iron deficiency anemia and/or nutritional megaloblastic anemias.



RE Iron Tablets Dosage and Administration


One tablet daily or as directed by a physician.



Contraindications


RE Iron Tablets 90mg is contraindicated in patients with known hypersensitivity to any of its ingredients. Folic acid (pteroylglutamic acid) is contraindicated in patients with untreated and uncomplicated pernicious anemia and in those with anaphylactic sensitivity to folic acid. Iron therapy is contraindicated in patients with hemochromatosis and patients with iron storage disease or the potential for iron stage disease dude to chronic hemolytic anemia (e.g., inherited anomalies of hemoglobin structure or synthesis and/or red cell enzyme deficiencies, etc.) pyridoxine responsive anemia or cirrhosis of the liver.



Warnings and Precautions


Accidental overdose of iron-containing products is a leading cause of fatal poisoning in children under 6. KEEP THIS PRODUCT OUT OF THE REACH OF CHILDREN. In case of accidental overdose, call a doctor or poison control center immediately.


General: Do not exceed recommended dose. The type of anemia and the underlying cause or causes should be determined before starting therapy with RE Iron Tablets 90mg. Since the anemia may be a result of a systemic disturbance, such as recurrent blood loss, the underlying cause or causes should be corrected, if possible.


Folic Acid: Folic acid in doses above 1.0 mg daily may obscure pernicious anemia.


Adverse Reactions


Allergic sensitivity reactions and gastrointestinal disturbances may occur with iron therapy. Folic Acid allergic sensitization has been reported following both oral and parenteral administration.


Call your doctor for medical advice about side effects. You may report side effects to the FDA at 1-800-FDA-1088.



Drug Interactions


There is a variety of iron/drug interactions which include antacids, tetracyclines, or fluoroquinolones.



USE IN SPECIFIC POPULATIONS


Pediatric Use: Safety and effectiveness in pediatric patients have not been established.


Geriatric Use: clinical studies on this product have not been performed in sufficient numbers of subjects aged 65 and over to determine whether elderly subjects respond differently from younger subjects,. In general, dose selection for an elderly patient should be made cautiously, usually starting at the low end of the dosing range, reflecting the greater frequency of decreased hepatic, renal, or cardiac function, and of concomitant disease or other drug therapy.



Overdosage


The clinical course of acute iron overdosage can vary. Initial symptoms may include abdominal pain, nausea, vomiting, diarrhea, tarry stools, melena, hematemesis, hypotension, tachycardia, metabolic acidosis, hyperglycemia, dehydration, drowsiness, pallor, cyanosis, lassitude, seizures, shock and coma.



RE Iron Tablets Description


Each reddish-brown, film-coated tablet for oral administration contains:

Iron (Carbonyl Iron) 90 mg

Folic Acid 1 mg

Vitamin B12 (Cyanocobalamin) 12 mcg

Vitamin C (Ascorbic acid) 120 mg

Docusate sodium 50 mg


Inactive ingredients: Sodium Benzoate, Silicon Dioxide, Microcrystalline Cellulose, Stearic Acid, Croscarmellose Sodium, Dicalcium Phosphate Dihydrate, Talc, FD&C Yellow No.6, FD&C Red No.40, FD&C Blue No.2, and Macrogol.


RE Iron Tablets - Clinical Pharmacology


Iron is necessary for the proper functioning of hemoglobin and red blood cell production.

Folic acid is required for cell division and growth and the maintenance of red blood cells.

Vitamin B12 is required for the maintenance of normal red blood cell synthesis, cell reproduction and normal growth. Intrinsic factor, a gastric protein secreted by the parietal cells, is required for the absorption of Vitamin B12 from the gastrointestinal tract.



Warning


Pernicious anemia should be ruled out before starting treatment. While folic acid corrects the hematological profile or pernicious anemia, it does not ameliorate the underlying neurologic involvement.



How Supplied/Storage and Handling


RE Iron Tablets 90 mg (NDC 68032-371-90) is a reddish-brown, modified rectangle shaped, film-coated tablet, debossed with “RE 371” on one side and blank on the other, and packaged in bottles of 90.


Store at 25C (77F). Excursions permitted to 15-30C (59-86F). (See USP Controlled Room Temperature.)

NOTICE: Contact with moisture can discolor or erode the tablet. Do not chew tablet.



PACKAGING










IRON 
iron pentacarbonyl  tablet










Product Information
Product TypeHUMAN PRESCRIPTION DRUGNDC Product Code (Source)68032-371
Route of AdministrationORALDEA Schedule    




















Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
IRON PENTACARBONYL (IRON)IRON PENTACARBONYL90 mg
FOLIC ACID (FOLIC ACID)FOLIC ACID1 mg
CYANOCOBALAMIN (CYANOCOBALAMIN)CYANOCOBALAMIN12 ug
ASCORBIC ACID (ASCORBIC ACID)ASCORBIC ACID120 mg
DOCUSATE SODIUM (SODIUM CATION)DOCUSATE SODIUM50 mg


























Inactive Ingredients
Ingredient NameStrength
SODIUM BENZOATE 
SILICON DIOXIDE 
CELLULOSE, MICROCRYSTALLINE 
STEARIC ACID 
CROSCARMELLOSE SODIUM 
DIBASIC CALCIUM PHOSPHATE DIHYDRATE 
TALC 
FD&C YELLOW NO. 6 
FD&C RED NO. 40 
FD&C BLUE NO. 2 
POLYETHYLENE GLYCOL 


















Product Characteristics
ColorbrownScoreno score
ShapeRECTANGLESize10mm
FlavorImprint CodeRE;371
Contains      










Packaging
#NDCPackage DescriptionMultilevel Packaging
168032-371-9090 TABLET In 1 BOTTLENone










Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
unapproved drug other04/01/200906/30/2011


Labeler - River's Edge Pharmaceuticals, LLC (133879135)
Revised: 12/2010River's Edge Pharmaceuticals, LLC

Sunday 25 October 2009

Hepaderm




Hepaderm may be available in the countries listed below.


Ingredient matches for Hepaderm



Sodium Alginate Sulfate

Sodium Alginate Sulfate is reported as an ingredient of Hepaderm in the following countries:


  • Japan

International Drug Name Search

Saturday 24 October 2009

Medamarin




Medamarin may be available in the countries listed below.


Ingredient matches for Medamarin



Lansoprazole

Lansoprazole is reported as an ingredient of Medamarin in the following countries:


  • Vietnam

International Drug Name Search

Sunday 18 October 2009

Gen-Amantadine




Gen-Amantadine may be available in the countries listed below.


Ingredient matches for Gen-Amantadine



Amantadine

Amantadine hydrochloride (a derivative of Amantadine) is reported as an ingredient of Gen-Amantadine in the following countries:


  • Canada

International Drug Name Search

Friday 16 October 2009

Cambia


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


CAMBIA (diclofenac potassium - for solution; oral)



  • Manufacturer: NAUTILUS NEUROSCIENC

    Approval date: June 17, 2009

    Strength(s): 50MG [RLD]

Has a generic version of Cambia been approved?


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


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




  • Pharmaceutical compositions based on Diclofenae
    Patent 6,974,595
    Issued: December 13, 2005
    Inventor(s): Reiner; Alberto & Reiner; Giorgio
    Assignee(s): ProEthic Pharmaceuticals, Inc.
    New pharmaceutical compositions for oral use containing Diclofenac together with alkali metal bicarbonates in amounts of from 20 to 80 by weight with respect to Diclofenac are described. These compositions are entirely palatable and free from any unpleasant taste or other side effects; in particular, these formulations permit to obtain in human patients higher Cmax of the active principle and shorter Tmax together with a lower coefficient of variation.
    Patent expiration dates:

    • May 15, 2017
      ✓ 
      Patent use: ACUTE TREATMENT OF MIGRAINE ATTACKS WITH OR WITHOUT AURA IN ADULTS




  • Pharmaceutical compositions and methods of treatment based on diclofenac
    Patent 7,482,377
    Issued: January 27, 2009
    Inventor(s): Reiner; Alberto & Reiner; Giorgio
    Assignee(s): Kowa Pharmaceuticals America, Inc.
    New pharmaceutical compositions for oral use containing diclofenac together with alkali metal bicarbonates in amounts of from 20 to 80 by weight with respect to diclofenac are described. These compositions are entirely palatable and free from any unpleasant taste or other, side effects; in particular, these formulations permit to obtain in human patients higher Cmax of the active principle and shorter Tmax together with a lower coefficient of variation.
    Patent expiration dates:

    • May 15, 2017
      ✓ 
      Patent use: ACUTE TREATMENT OF MIGRAINE ATTACKS WITH OR WITHOUT AURA IN ADULTS
      ✓ 
      Drug substance
      ✓ 
      Drug product




  • Diclofenac formulations and methods of use
    Patent 7,759,394
    Issued: July 20, 2010
    Inventor(s): Reiner; Giorgio & Reiner; Alberto & Meyer; Andreas
    Assignee(s): APR Applied Pharma Research SA
    Methods and formulations are provided for treating migraine and other acute pain episodes using diclofenac, and formulations of diclofenac that provide both rapid and sustained relief from acute pain. Methods and formulations are also provided for treating symptoms that often accompany migraine and acute pain such as photophobia, phonophobia, nausea and vomiting.
    Patent expiration dates:

    • June 16, 2026
      ✓ 
      Patent use: ACUTE TREATMENT OF MIGRAINE ATTACKS WITH OR WITHOUT AURA IN ADULTS
      ✓ 
      Drug substance
      ✓ 
      Drug product




  • Diclofenac formulations and methods of use
    Patent 8,097,651
    Issued: January 17, 2012
    Inventor(s): Reiner; Giorgio & Reiner; Alberto & Meyer; Andreas
    Assignee(s): APR Applied Pharma Research s.a.
    Methods and formulations are provided for treating migraine and other acute pain episodes using diclofenac, and formulations of diclofenac that provide both rapid and sustained relief from acute pain. Methods and formulations are also provided for treating symptoms that often accompany migraine and acute pain such as photophobia, phonophobia, nausea and vomiting.
    Patent expiration dates:

    • June 16, 2026
      ✓ 
      Patent use: ACUTE TREATMENT OF MIGRAINE ATTACKS WITH OR WITHOUT AURA IN ADULTS
      ✓ 
      Drug substance
      ✓ 
      Drug product



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:
    • June 17, 2012 - NEW DOSAGE FORM

See also...

  • Cambia Consumer Information (Drugs.com)
  • Cambia Powder Packets Consumer Information (Wolters Kluwer)
  • Cambia Consumer Information (Cerner Multum)
  • Cambia Advanced Consumer Information (Micromedex)
  • Diclofenac Consumer Information (Drugs.com)
  • Diclofenac Consumer Information (Wolters Kluwer)
  • Diclofenac Enteric-Coated Tablets Consumer Information (Wolters Kluwer)
  • Diclofenac Extended-Release Tablets Consumer Information (Wolters Kluwer)
  • Diclofenac Immediate-Release Tablets Consumer Information (Wolters Kluwer)
  • Diclofenac Potassium Powder Packets Consumer Information (Wolters Kluwer)
  • Diclofenac Consumer Information (Cerner Multum)
  • Diclofenac Advanced Consumer Information (Micromedex)
  • Diclofenac Potassium AHFS DI Monographs (ASHP)
  • Diclofenac Sodium AHFS DI Monographs (ASHP)
  • Diclofenac epolamine AHFS DI Monographs (ASHP)

Thursday 15 October 2009

Grifonimod




Grifonimod may be available in the countries listed below.


Ingredient matches for Grifonimod



Nimodipine

Nimodipine is reported as an ingredient of Grifonimod in the following countries:


  • Chile

International Drug Name Search

Wednesday 14 October 2009

Banex-LA


Generic Name: guaifenesin and phenylpropanolamine (gwye FEN e sin/fen ill proe pa NOLE a meen)

Brand Names: Ami-Tex LA, Banex-LA, Coldloc-LA, Dayquil Sinus Pressure and Congestion, Despec, Entex LA, Exgest LA, G-Vent, Guaifenex PPA 75, Guaivent, Guiatex LA, Naldecon-EX Pediatric, Nasahist LA, Phentex-LA, Phenylfenesin LA, Poly-Vent, Profen LA, Stamoist LA, Triaminic Expectorant, Vanex-LA


What is Banex-LA (guaifenesin and phenylpropanolamine)?

Guaifenesin is an expectorant. It is used to break up congestion and mucous to make breathing easier. Guaifenesin thins mucous, increases lubrication of the respiratory tract (lungs, nose and throat), and increases the removal of mucous.


Phenylpropanolamine is a decongestant. It constricts (shrinks) blood vessels (veins and arteries), which reduces swelling of mucous membranes in areas such as the nose and sinuses.


Guaifenesin and phenylpropanolamine is used to treat the symptoms of the common cold and of infections of the sinuses, lungs, and throat.


Phenylpropanolamine, an ingredient in this product, has been associated with an increased risk of hemorrhagic stroke (bleeding into the brain or into tissue surrounding the brain) in women. Men may also be at risk. Although the risk of hemorrhagic stroke is low, the U.S. Food and Drug Administration (FDA) recommends that consumers not use any products that contain phenylpropanolamine.


Guaifenesin and phenylpropanolamine may also be used for purposes other than those listed in this medication guide.


What is the most important information I should know about Banex-LA (guaifenesin and phenylpropanolamine)?


Phenylpropanolamine, an ingredient in this product, has been associated with an increased risk of hemorrhagic stroke (bleeding into the brain or into tissue surrounding the brain) in women. Men may also be at risk. Although the risk of hemorrhagic stroke is low, the U.S. Food and Drug Administration (FDA) recommends that consumers not use any products that contain phenylpropanolamine.


Drink plenty of extra fluids while taking this medication. Do not crush or chew the tablets. Swallow them whole or break them in half where they are scored to make them easier to swallow if needed.

Who should not take Banex-LA (guaifenesin and phenylpropanolamine)?


Do not take guaifenesin and phenylpropanolamine if you have taken a monoamine oxidase inhibitor (MAOI) such as isocarboxazid (Marplan), phenelzine (Nardil), or tranylcypromine (Parnate) in the last 14 days. A dangerous drug interaction could occur, leading to serious side effects.

Before taking this medication, tell your doctor if you have



  • high blood pressure or any other type of heart disease,




  • diabetes,




  • a peripheral vascular disorder (poor circulation),




  • glaucoma or increased pressure in the eyes,




  • an overactive thyroid, or




  • difficulty urinating or an enlarged prostate.



You may not be able to take guaifenesin and phenylpropanolamine, or you may require a dosage adjustment or special monitoring during treatment if you have any of the conditions listed above.


Guaifenesin and phenylpropanolamine is in the FDA pregnancy category C. This means that it is not known whether guaifenesin and phenylpropanolamine will harm an unborn baby. Do not take this medication without first talking to your doctor if you are pregnant. This medication passes into breast milk and may harm a nursing baby. Do not take this medication without first talking to your doctor if you are breast-feeding a baby. If you are over 65 years of age, you may be more likely to experience side effects from guaifenesin and phenylpropanolamine. You may require a lower dose of this medication. Guaifenesin and phenylpropanolamine has not been approved for use by children younger than 6 years of age.

How should I take Banex-LA (guaifenesin and phenylpropanolamine)?


Take guaifenesin and phenylpropanolamine exactly as directed by your doctor. If you do not understand these directions, ask your pharmacist, nurse, or doctor to explain them to you.


Take each dose with a full glass of water. Increasing fluid intake during the day may help relieve congestion. Take guaifenesin and phenylpropanolamine with food if it causes stomach upset. Do not crush or chew the tablets. Swallow them whole or break them in half where they are scored to make them easier to swallow if needed. Store guaifenesin and phenylpropanolamine at room temperature away from moisture and heat.

What happens if I miss a dose?


Take the missed dose as soon as you remember. However, if it is almost time for the next dose, skip the missed dose and take only the next regularly scheduled dose. Do not take a double dose of this medication.


What happens if I overdose?


Seek emergency medical attention.

Symptoms of a guaifenesin and phenylpropanolamine overdose include vomiting, high blood pressure (headache, redness of face, blurred vision), an irregular heartbeat, and numbness of the fingers or toes.


What should I avoid while taking Banex-LA (guaifenesin and phenylpropanolamine)?


Use caution when driving, operating machinery, or performing other hazardous activities. Guaifenesin and phenylpropanolamine may cause dizziness. If you experience dizziness, avoid these activities.

Banex-LA (guaifenesin and phenylpropanolamine) side effects


No serious side effects from guaifenesin and phenylpropanolamine are expected. Seek emergency medical attention if you experience an allergic reaction (difficulty breathing; closing of your throat; swelling of your lips, tongue, or face; or hives).

Other, less serious side effects may be more likely to occur. Continue to take guaifenesin and phenylpropanolamine and talk to your doctor if you experience



  • dizziness or headache;




  • nervousness, restlessness, or insomnia;




  • nausea or stomach upset; or




  • difficulty urinating.



Side effects other than those listed here may also occur. Talk to your doctor about any side effect that seems unusual or that is especially bothersome.


What other drugs will affect Banex-LA (guaifenesin and phenylpropanolamine)?


Do not take guaifenesin and phenylpropanolamine if you have taken a monoamine oxidase inhibitor (MAOI) such as isocarboxazid (Marplan), phenelzine (Nardil), or tranylcypromine (Parnate) in the last 14 days. A dangerous drug interaction could occur, leading to serious side effects.

Heart medications such as methyldopa (Aldomet), reserpine (Serpalan, Serpasil), and guanethidine (Ismelin) may have decreased effects. Talk to your doctor before taking guaifenesin and phenylpropanolamine if you are taking any of these medications.


Do not take other over-the-counter cough, cold, allergy, diet, or sleep aids while taking guaifenesin and phenylpropanolamine without first talking to your doctor or pharmacist. Other medications may also contain guaifenesin, phenylpropanolamine, or other similar drugs. You may accidentally take too much of these medicines.


Drugs other than those listed here may also interact with guaifenesin and phenylpropanolamine. Talk to your doctor and pharmacist before taking any prescription or over-the-counter medicines.



More Banex-LA resources


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


Compare Banex-LA with other medications


  • Cough and Nasal Congestion


Where can I get more information?


  • Your pharmacist has additional information about guaifenesin and phenylpropanolamine written for health professionals that you may read.

What does my medication look like?


Guaifenesin and phenylpropanolamine is available with a prescription under several brand names. Ask your pharmacist any questions you have about this medication, especially if it is new to you.



  • Entex LA, 400 mg of guaifenesin and 75 mg of phenylpropanolamine--orange, scored tablets




  • Exgest LA, 400 mg of guaifenesin and 75 mg of phenylpropanolamine--white, oval-shaped, scored, long-acting tablets with blue speckles




  • Dura-Vent, 600 mg of guaifenesin and 75 mg of phenylpropanolamine--white, scored tablets



See also: Banex-LA side effects (in more detail)