Search Weight Loss Topics:

Home » Long Term Weight Loss » Qnexa Obesity Drug – FDA Concerned About Long-term Side Effects

Editor's Choice
Main Category: Obesity / Weight Loss / Fitness
Also Included In: Regulatory Affairs / Drug Approvals
Article Date: 19 Feb 2012 - 0:00 PST

email to a friend   printer friendly   opinions  

Current Article Ratings:

Patient / Public:

2 (3 votes)

Healthcare Prof:
The FDA has expressed concerned regarding obesity drug Qnexa - a combination of phentermine and topiramate - and what associations there may be between long-term usage and birth defect risks, as well as its impact on the heart. The Food and Drug Administration (FDA) is reviewing Qnexa again, after turning down its submission for approval two years ago ("FDA Turns Down Weight Loss Drug Qnexa, But Makers See Short Timeline For Approval").

There is an FDA Advisory Panel (Endocrinologic and Metabolic Drugs Advisory Committee) meeting on 22 February. The Panel will look at 2-years' worth of clinical data. When Qnexa was last reviewed, the Agency only had 1-year's worth of data to look at.

The Advisory Panel consists of experts, none of whom work for the FDA. They will have to discuss and vote on whether to recommend supporting or declining the obesity drug after carrying out an overall benefit-risk assessment. The Panel's recommendation is not binding; the FDA can choose to ignore it; but this hardly ever happens. Therefore, Qnexa's future, at least this time round, depends on what happens this coming Wednesday.

When the FDA turned Qnexa down, it asked its makers Vivus Inc. for more clinical data on the medication's potential impact on major adverse cardiovascular events and birth defects.

The FDA now acknowledges that studies have demonstrated that Qnexa can help patients lose a considerable amount of weight during the initial 12 months of treatment. The Agency added that a number of participants put some of their lost weight back on during their second year. Concerns regarding birth defects and accelerated heartbeat were raised again.

Qnexa is a combination of phentermine and topiramate. Studies on topiramate have indicated that there may be a higher chance of having babies with birth defects. According to the FDA, pregnant women who are exposed to topiramate might have a higher risk of giving birth to babies with oral clefts.

At first, Vivus suggested limiting Qnexa use to adult males and females of specific age groups (non-child bearing ages). According to Vivus, the FDA responded by asking the company to come up with a plan of limited usage by pregnant women.

Qnexa consists of:

Phetermine, chemical formula C10H15N - a psychostimulant appetite suppressor. Its pharmacology is similar to amphetamine. Medically, it is currently used to suppress appetite. Topiramate, chemical formula C12H21NO8S - an anti-epilepsy (anticonvulsant) medication which also increases the sensation of feeling full (of food). Psychiatrists sometimes use topiramate for bipolar disorder. It is currently being investigated for the treatment of alcoholism The pharmaceutical industry has tried, mostly unsuccessfully, to bring new anti-obesity medications onto the market. Meridia, an Abbot Laboratories drug, was taken off the market in 2010 after it was linked to stroke and heart attack risk.

Written by Christian Nordqvist

Copyright: Medical News Today
Not to be reproduced without permission of Medical News Today Visit our obesity / weight loss / fitness section for the latest news on this subject.

Sources: FDA, Vivus, Medical News Today archives

Please use one of the following formats to cite this article in your essay, paper or report:

MLA

Christian Nordqvist. "Qnexa Obesity Drug - FDA Concerned About Long-term Side Effects." Medical News Today. MediLexicon, Intl., 19 Feb. 2012. Web.
19 Feb. 2012. <http://www.medicalnewstoday.com/articles/241873.php&gt;

APA

Please note: If no author information is provided, the source is cited instead.

Rate this article:
(Hover over the stars then click to rate) Patient / Public:
or Health Professional:

Please note that we publish your name, but we do not publish your email address. It is only used to let you know when your message is published. We do not use it for any other purpose. Please see our privacy policy for more information.

If you write about specific medications or operations, please do not name health care professionals by name.

All opinions are moderated before being included (to stop spam)

Contact Our News Editors

For any corrections of factual information, or to contact the editors please use our feedback form.

Please send any medical news or health news press releases to:

Note: Any medical information published on this website is not intended as a substitute for informed medical advice and you should not take any action before consulting with a health care professional. For more information, please read our terms and conditions.

Read more here:
Qnexa Obesity Drug - FDA Concerned About Long-term Side Effects

Your Full Name
Your Email
Your Phone Number
Select your age (30+ only)	30313233343536373839404142434445464748495051525354555657585960616263646566676869707172737475767778798081828384858687888990919293949596979899100101102103104105106107108109110111112113114115116117118119120
Select Your US State	Select Your StateAlabamaAlaskaArizonaArkansasCaliforniaColoradoConnecticutDelawareFloridaGeorgiaHawaiiIdahoIllinoisIndianaIowaKansasKentuckyLouisianaMaineMarylandMassachusettsMichiganMinnesotaMississippiMissouriMontanaNebraskaNevadaNew HampshireNew JerseyNew MexicoNew YorkNorth CarolinaNorth DakotaOhioOklahomaOregonPennsylvaniaRhode IslandSouth CarolinaSouth DakotaTennesseeTexasUtahVermontVirginiaWashingtonWashington,DCWest VirginiaWisconsinWyoming
Program Choice	Select Your ProgramInjectable HGHInjectable TestoteroneInjectable SermorelinInjectable Weight LossInjectable HCG DietInjectable Vitamins
Confirm over 30 years old	Yes
Confirm that you resident in USA	Yes
This is a Serious Inquiry	Yes
Message:

Home » Long Term Weight Loss » Qnexa Obesity Drug – FDA Concerned About Long-term Side Effects