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**NOTE** - has claimed original rights on [link widoczny dla zalogowanych] the article "Zelnorm: Anatomy of a Potentially Dangerous Drug" ... if there is a dispute on the originality of this article ... please contact us via our and supply our staff with the appropriate details of dispute (ie ).
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Zelnorm is also known by its generic name, Tegaserod, and is considered a 5-HT 4 agonist. Novartis
manufactures the drug for use in the management of constipation and IBS (irritable bowel syndrome).
The drug was originally FDA approved in 2002; however, in late March of 2007, it was pulled off the
market as the FDA believed it may have been causing unfavorable cardiovascular effects.
Prior to its market removal, Zelnorm was the one and only drug that the FDA had approved to assist with
the relief of the symptoms of irritable bowel syndrome and chronic [link widoczny dla zalogowanych] constipation. The drug acted as a
stimulant for motility to stimulate gastrointestinal system motility as well as peristaltic reflex. Many
claimed that the drug also reduced the [link widoczny dla zalogowanych] abdominal pain associated with [link widoczny dla zalogowanych] these issues.
Zelnorm had several reported side effects that were reported after studies had been conducted. [link widoczny dla zalogowanych] These
side effects can range from the minor and more common to the more extreme and serious and include:
- Body [link widoczny dla zalogowanych] - Abdominal pain, facial edema, flushing
- Cardiovascular effects - angina pectoris, arrhythmia, heart attack, hypertension, hypotension,
- stroke, syncope
- Central Nervous System - Anxiety, vertigo
- Female Reproductive System - unusually heavy menstrual bleeding, ovarian cysts
- Gastrointestinal - severe diarrhea, ischemic colitis
- Neoplasms - can cause breast cancer
- Psychiatric - anxiety, depression, concentration issues, appetite increaser, sleep disorders
- Skin - severe itching and increased sweating
The symptoms listed above that occurred most often in patients taking Zelnorm were the gastrointestinal
and cardiovascular symptoms. Obviously, this was a major issue that the FDA noted in their decision to
pull the drug altogether.
The FDA was prompted to [link widoczny dla zalogowanych] pull Zelnorm from the U.S. market after receiving results of an analysis that
had been performed on the drug. This analysis clearly linked Zelnorm to serious cardiovascular issues
which included stroke and heart attack. Since the drug has been removed, the FDA encourages anyone
still using the drug to get medical attention as soon as possible if they should begin experiencing
dizziness, chest pain, [link widoczny dla zalogowanych] shortness of breath, numbness, drooping eyelids, altered senses or any other stroke or heart attack symptoms.
Zelnorm was first approved, despite Public Citizen's petitions to stop the approval, for use in women who
had been suffering with IBS in 2002, albeit for short-term use only. Two years later, the FDA approved an expansion of Zelnorm's uses. This expansion involved the drug being approved for women under 65 to use the drug for the treatment of chronic idiopathic constipation.
As previously touched on, the FDA's decision was based on nearly 30 studies that [link widoczny dla zalogowanych] involved in excess of
18,000 patients. What these studies revealed was that Zelnorm increased the [link widoczny dla zalogowanych] patient's risk of stroke,
heart attack and angina. The FDA strongly recommends that anyone still using Zelnorm seriously consider halting use of the drug. This is especially true in patients that have recently developed hypotension, syncope, diarrhea, and ischemic colitis.
The FDA further stated that [link widoczny dla zalogowanych] it has concluded that Zelnorm and any benefits that patients may see from
its use fails to outweigh the risks associated with the drug for the majority of patients that it was initially
approved for.
If you have experienced serious side effects as a result of taking Zelnorm, a lawyer with experience in
the ongoing Zelnorm side effects lawsuit can help evaluate your claim at no charge. The Zelnorm
attorneys at JD Law Group are qualified to review your claim. You [link widoczny dla zalogowanych] can contact them directly via 1-888-
736-4248 or by filling out the contact form at the bottom of this page.
DISCLAIMER: The information provided on this website or the web site linked here in are not a substitute
for professional medical or legal advice, diagnosis or treatment. In addition, viewing the content on
these websites, requesting additional information, or transmitting information through a contact form
does not form an attorney-client relationship with the sponsoring attorney. Any results set forth herein
are based upon the facts of that particular case or scientific study and [link widoczny dla zalogowanych] do not represent a promise or
guaranty regarding similar outcome or causes. The information on this site is intended for educational
purposes only [link widoczny dla zalogowanych] and should never interfere with a patient/site visitor and his or her healthcare provider.
Internet subscribers or online readers should not act upon any information contained herein without
seeking professional legal and/or medical advice. This firm is licensed to practice law only in the state of
California, but is affiliated with a network of licensed attorneys in other states. Call 911 for all [link widoczny dla zalogowanych] medical
emergencies. Drug-Recalls.org and JD Law Group makes no representation or warranty regarding the
accuracy, reliability, completeness, currentness, or timeliness of the content, text or graphics. Links to
other sites are provided for information only - they do not constitute endorsements of those other
sites.
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DrugRecalls.org is a free resource about recalled or questionable drugs. The Zelnorm litigation attorneys at JD Law Group specialize in helping people victims of questionable drugs. Call them at 1-888-736-4248 if you have been seriously injured by a prescription drug.
Zelnorm: Anatomy of a Potentially Dangerous DrugArticle Summary: Zelnorm was first approved, [link widoczny dla zalogowanych] despite Public Citizen's petitions to stop the approval, for use in women whohad been suffering with IBS in 2002, albeit for short-term use only. Two years later, the [link widoczny dla zalogowanych] FDA approved an expansion of Zelnorm's uses.