Dofetilide Side Effects

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Dofetilide Safety Reports

Total Dofetilide reports: 7.
Dofetilide FDA safety alerts: No.
Reported deaths: 2    Reported hospitalizations: 1.
Take Dofetilide Side Effects Survey or Share Your Dofetilide Story.
Reported Dofetilide Side Effects: atrial fibrillation, non-hodgkin's lymphoma, renal failure, ventricular tachycardia, torsade de pointes, pulmonary oedema, pulmonary congestion, osteonecrosis, condition aggravated, chest pain, atrial flutter.
More About Dofetilide.

Dofetilide Side Effects Report #5196295-X
Health Professional from UNITED KINGDOM reported DOFETILIDE problem on Dec 22, 2006. Male patient, 69 years of age, weighting 181.7 lb, was diagnosed with atrial fibrillation and was treated with DOFETILIDE. After drug was administered, patient experienced the following problems/side effects: haemangioma of liver, non-hodgkin's lymphoma. DOFETILIDE dosage: unknown. During the same period patient was treated with DILTIAZEM, ENALAPRIL MALEATE, ATORVASTATIN CALCIUM, WARFARIN, VENTOLIN. Patient recovered.

Dofetilide Side Effects Report #5243572-X
DOFETILIDE problem was reported by a Consumer or non-health professional from UNITED STATES on Feb 20, 2007. Male patient, 66 years of age, weighting 203.9 lb, was treated with DOFETILIDE. After drug was administered, patient experienced the following problems/side effects: electrocardiogram qt prolonged. DOFETILIDE dosage: unknown. Patient recovered.

Dofetilide Side Effects Report #5288942-9
Consumer or non-health professional from UNITED KINGDOM reported DOFETILIDE problem on Mar 28, 2007. Male patient, 69 years of age, weighting 181.7 lb, was diagnosed with atrial fibrillation and was treated with DOFETILIDE. After drug was administered, patient experienced the following problems/side effects: non-hodgkin's lymphoma. DOFETILIDE dosage: unknown. During the same period patient was treated with DILTIAZEM, ENALAPRIL MALEATE, ATORVASTATIN CALCIUM, WARFARIN, SALBUTAMOL. Patient recovered.

Dofetilide Side Effects Report #5319343-2
DOFETILIDE problem was reported by a Health Professional from UNITED KINGDOM on Apr 27, 2007. Male patient, weighting 176.4 lb, was diagnosed with arrhythmia and was treated with DOFETILIDE. After drug was administered, patient experienced the following problems/side effects: acute left ventricular failure, arrhythmia, atrial fibrillation, atrial flutter, chest pain, condition aggravated, osteonecrosis, pulmonary congestion, pulmonary oedema. DOFETILIDE dosage: unknown. During the same period patient was treated with METOPROLOL SUCCINATE, WARFARIN, LAMOTRIGINE, TEMAZEPAM. Patient was hospitalized. Patient died on 02/08/2007.

Dofetilide Side Effects Report #5162485-5
Pharmacist from UNITED STATES reported DOFETILIDE problem on Nov 29, 2006. Male patient, 86 years of age, was diagnosed with atrial fibrillation and was treated with DOFETILIDE. After drug was administered, patient experienced the following problems/side effects: torsade de pointes, ventricular tachycardia. DOFETILIDE dosage: unknown. During the same period patient was treated with LEVOTHYROXINE, RAMIPRIL, METOPROLOL, WARFARIN, FUROSEMIDE. Patient recovered.

Dofetilide Side Effects Report #5209703-2
DOFETILIDE problem was reported by a Pharmacist from UNITED STATES on Nov 10, 2005. Female patient, weighting 120.0 lb, was diagnosed with atrial fibrillation and was treated with DOFETILIDE. After drug was administered, patient experienced the following problems/side effects: atrial fibrillation. DOFETILIDE dosage: 0.25 (0.125 MG, BID INTERVAL: EVERY DAY). During the same period patient was treated with COREG, METOPROLOL TARTRATE, DILTIAZEM, CARDIZEM, QUINIDINE, CLINDAMYCIN. Patient recovered.

Dofetilide Side Effects Report #5418949-X
Health Professional from UNITED KINGDOM reported DOFETILIDE problem on Aug 07, 2007. Male patient, 42 years of age, was treated with DOFETILIDE. After drug was administered, patient experienced the following problems/side effects: renal failure. DOFETILIDE dosage: unknown. Patient died.


Drug Information: Dofetilide

URL of this page: http://www.nlm.nih.gov/medlineplus/druginfo/medmaster/a601235.html

(doe fet' il ide)

IMPORTANT WARNING:

Tikosyn can cause your heart to beat irregularly. You will need to be in a hospital or another place where you can be monitored closely by your doctor for at least 3 days when you are started or restarted on dofetilide. It is important to read the patient information provided to you every time you begin therapy with dofetilide.

Why is this medication prescribed?

Dofetilide is used to treat irregular heartbeats. It improves your heart rhythm by relaxing an overactive heart.

This medication is sometimes prescribed for other uses; ask your doctor or pharmacist for more information.

How should this medicine be used?

Dofetilide comes as a capsule to take by mouth. It is usually taken twice a day. Follow the directions on your prescription label carefully, and ask your doctor or pharmacist to explain any part you do not understand. Take dofetilide exactly as directed. Do not take more or less of it or take it more often than prescribed by your doctor. Do not take a double dose.

Dofetilide controls abnormal heart rhythms but does not cure them. Continue to take dofetilide even if you feel well. Do not stop taking dofetilide without talking to your doctor.

What special precautions should I follow?

Before taking dofetilide,

  • tell your doctor and pharmacist if you are allergic to dofetilide or any other drugs.
  • tell your doctor and pharmacist what prescription and nonprescription medications you are taking, especially antipsychotics, bepridil (Vascor), cimetidine (Tagamet), cisapride (Propulsid), clarithromycin (Biaxin), diltiazem (Cardizem), diuretics ('water pills'), erythromycin (E.E.S., E-Mycin, others), HIV protease inhibitors such as ritonavir (Norvir), itraconazole (Sporanox), ketoconazole (Nizoral), medications for dizziness or nausea, medications for depression such as amitriptyline (Elavil) or fluoxetine (Prozac), megestrol (Megace), metformin (Glucophage), other medications for irregular heart beats such as amiodarone (Cordarone), norfloxacin (Noroxin), prochlorperazine (Compazine), quinine (Formula Q), trimethoprim (Proloprim, Trimpex), trimethoprim and sulfamethoxazole (Bactrim, Septra), verapamil (Calan, Covera, Verelan), zafirlukast (Accolate), and vitamins.
  • tell your doctor if you have or have ever had long QT syndrome (a type of heart problem), or kidney or liver disease.
  • tell your doctor if you are pregnant, plan to become pregnant, or are breast-feeding. If you become pregnant while taking dofetilide, call your doctor.

What special dietary instructions should I follow?

Talk to your doctor before drinking grapefruit juice. It may be best to drink other fruit juices while taking dofetilide.

What should I do if I forget a dose?

Skip the missed dose and continue your regular dosing schedule. Do not take a double dose to make up for a missed one.

What side effects can this medication cause?

Dofetilide may cause side effects. Tell your doctor if any of these symptoms are severe or do not go away:

  • headache
  • chest pain
  • dizziness
  • respiratory infection
  • flu-like symptoms
  • stomach pain
  • back pain
  • diarrhea
  • difficulty sleeping

If you experience any of the following symptoms, call your doctor immediately:

  • irregular heartbeat
  • rash
  • sweating
  • upset stomach
  • vomiting
  • loss of appetite or thirst

If you experience a serious side effect, you or your doctor may send a report to the Food and Drug Administration's (FDA) MedWatch Adverse Event Reporting program online [at http://www.fda.gov/MedWatch/index.html] or by phone [1-800-332-1088].

What storage conditions are needed for this medicine?

Keep this medication in the container it came in, tightly closed, and out of reach of children. Store it at room temperature and away from excess heat and moisture (not in the bathroom). Throw away any medication that is outdated or no longer needed. Talk to your pharmacist about the proper disposal of your medication.

In case of emergency/overdose

In case of overdose, call your local poison control center at 1-800-222-1222. If the victim has collapsed or is not breathing, call local emergency services at 911.

What other information should I know?

Keep all appointments with your doctor and the laboratory. Your heart rhythm should be checked regularly to determine your response to dofetilide. Your doctor will also want to follow your kidney function and blood level of potassium closely while you are taking dofetilide.

If you are ill for more than 24 hours with diarrhea, vomiting, or sweating and have not been able to take in much fluid or nutrition you should call your doctor before taking your next dose of dofetilide.

Do not let anyone else take your medication. Ask your pharmacist any questions you have about refilling your prescription.

It is important for you to keep a written list of all of the prescription and nonprescription (over-the-counter) medicines you are taking, as well as any products such as vitamins, minerals, or other dietary supplements. You should bring this list with you each time you visit a doctor or if you are admitted to a hospital. It is also important information to carry with you in case of emergencies.

Brand name(s):

  • Tikosyn®

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ALABAMA
ALASKA
AMERICAN SAMOA
ARIZONA
ARKANSAS
CALIFORNIA
COLORADO
CONNECTICUT
DELAWARE
DISTRICT OF COLUMBIA
FEDERATED STATES OF MICRONESIA
FLORIDA
GEORGIA
GUAM
HAWAII
IDAHO
ILLINOIS
INDIANA
IOWA
KANSAS
KENTUCKY
LOUISIANA
MAINE
MARSHALL ISLANDS
MARYLAND
MASSACHUSETTS
MICHIGAN
MINNESOTA
MISSISSIPPI
MISSOURI
MONTANA
NEBRASKA
NEVADA
NEW HAMPSHIRE
NEW JERSEY
NEW MEXICO
NEW YORK
NORTH CAROLINA
NORTH DAKOTA
NORTHERN MARIANA ISLANDS
OHIO
OKLAHOMA
OREGON
PALAU
PENNSYLVANIA
PUERTO RICO
RHODE ISLAND
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SOUTH DAKOTA
TENNESSEE
TEXAS
UTAH
VERMONT
VIRGIN ISLANDS
VIRGINIA
WASHINGTON
WEST VIRGINIA
WISCONSIN
WYOMING
PatientsVille.com does not provide medical advice, diagnosis or treatment. The information contained on PatientsVille.com site has not been scientifically or otherwise verified as to a cause and effect relationship and cannot be used to estimate the incidence of adverse drug reactions or for establishing or changing of patient treatments.


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