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Vioxx

Osteoarthritis facts

  • Osteoarthritis is a joint inflammation that results from cartilage degeneration.
  • Osteoarthritis can be caused by aging, heredity, and injury from trauma or disease.
  • The most common symptom of osteoarthritis is pain in the affected joint(s) after repetitive use.
  • There is no blood test for the diagnosis of osteoarthritis.
  • The goal of treatment in osteoarthritis is to reduce joint pain and inflammation while improving and maintaining joint function.

What is osteoarthritis?

Osteoarthritis is a form of arthritis that features the breakdown and eventual loss of the cartilage of one or more joints. Cartilage is a protein substance that serves as a "cushion" between the bones of the joints. Among the over 100 different types of arthritis conditions, osteoarthritis is the most common, affecting over 25 million people in the United Stat...

Vioxx

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Discontinued Warning IconPlease Note: This Brand Name drug is no longer available in the US.
(Generic versions may still be available.)

Vioxx Patient Information Including Side Effects

Brand Names: Vioxx

Generic Name: rofecoxib (oral) (Pronunciation: row feh COCK sib)

What is rofecoxib (Vioxx)?

Rofecoxib (Vioxx) was withdrawn from the U.S. market in 2004.

Rofecoxib is in a class of drugs called nonsteroidal anti-inflammatory drugs (NSAIDs). Rofecoxib works by reducing substances that cause inflammation, pain, and fever in the body.

Rofecoxib is used to reduce pain, inflammation, and stiffness caused by osteoarthritis, rheumatoid arthritis and certain forms of juvenile rheumatoid arthritis; to manage acute pain in adults; to treat migraines; and to treat menstrual pain.

Rofecoxib may also be used for purposes other than those listed in this medication guide.

What are the possible side effects of rofecoxib (Vioxx)?

Notify your doctor immediately if you develop abdominal pain, tenderness, or discomfort; nausea; blood in your vomit; bloody, black, or tarry stools; unexplained weight gain; swelling or water retention; fatigue or lethargy; a skin rash; itching; yellowing of your skin or eyes;"flu-like" symptoms; or unusual bruising or bleeding. These symptoms could be early signs of dangerous side effects.

If you experience any of the following serious side effects, stop taking rofecoxib and seek medical treatment or contact your doctor immediately:

  • an allergic reaction (difficulty breathing; closing of your throat; swelling of your lips, tongue, or face; or hives);
  • abdominal pain, tenderness, or discomfort;
  • bloody, black, or tarry stools;
  • nausea or heartburn;
  • blood in your vomit;
  • unexplained weight gain;
  • swelling or water retention;
  • unusual fatigue or lethargy;
  • a skin rash or itching;
  • yellowing of your skin or eyes;
  • "flu-like" symptoms; or
  • unusual bruising or bleeding.

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

  • dizziness;
  • mild fatigue or weakness; or
  • diarrhea.

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 is the most important information I should know about rofecoxib (Vioxx)?

Rofecoxib (Vioxx) was withdrawn from the U.S. market in 2004.

The manufacturer of rofecoxib (Vioxx) has announced a voluntary withdrawal of the drug from the U.S. and worldwide market. This withdrawal is due to safety concerns of an increased risk of cardiovascular events (including heart attack and stroke) in patients taking rofecoxib.

Notify your doctor immediately if you develop abdominal pain, tenderness, or discomfort; nausea; blood in your vomit; bloody, black, or tarry stools; unexplained weight gain; swelling or water retention; fatigue or lethargy; a skin rash; itching; yellowing of your skin or eyes;"flu-like" symptoms; or unusual bruising or bleeding. These symptoms could be early signs of dangerous side effects.

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Report Problems to the Food and Drug Administration

 

You are encouraged to report negative side effects of prescription drugs to the FDA. Visit the FDA MedWatch website or call 1-800-FDA-1088.


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