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VIVUS Inc. Message Board

  • mooky8639 mooky8639 Jan 17, 2013 11:51 AM Flag

    ARNA HAS $1BILLION MORE MARKET CAP THAN VVUS?

    Go figure and VVUS is over valuated with 2 FDA approved products.?

    Sentiment: Strong Buy

    SortNewest  |  Oldest  |  Most Replied Expand all replies
    • At this time VVUS is overvalued. Just maybe in a year or two they will be selling more if they can adjust price and put out those ads. Going it alone is bad for business. Pozn and SOMX, Amrn are a few who begain this way and what did it get them but low market sales with little advertising and a stock that got crushed. Amrn is just learning what the street thinks about their sales plan.

      Sentiment: Hold

    • ARNA will be crushed once it gets to the market. Right now ARNA investors are in a delusional; state thinking that their placebo has a chance in the market. Drop out rate for belviq will set a record as no sane person would want to spend money and risk unknown side effects so maybe if the get lucky they lose %5...!!
      ARNA's $2.3 BILLION market cap is gift from the heavens to the shorts ... LOL

    • both products are garbage!!!hedgeies approved it not the fda people are smarter than that i bet nobody at vivus will give it to their family members

    • Important Safety Information

      Qsymia is contraindicated in pregnancy; in patients with glaucoma; in hyperthyroidism; in patients receiving treatment or within 14 days following treatment with monoamine oxidase inhibitors (MAOIs); or in patients with hypersensitivity to sympathomimetic amines, topiramate, or any of the inactive ingredients in Qsymia.

      Qsymia can cause fetal harm. Females of reproductive potential should have a negative pregnancy test before treatment and monthly thereafter and use effective contraception consistently during Qsymia therapy. If a patient becomes pregnant while taking Qsymia, treatment should be discontinued immediately, and the patient should be informed of the potential hazard to the fetus.

      Qsymia can cause an increase in resting heart rate. Regular measurement of resting heart rate is recommended for all patients taking Qsymia, especially patients with cardiac or cerebrovascular disease or when initiating or increasing the dose of Qsymia. Qsymia has not been studied in patients with recent or unstable cardiac or cerebrovascular disease and therefore use is
      not recommended.

      Topiramate, a component of Qsymia, increases the risk of suicidal thoughts or behavior in patients taking these drugs for any indication. Patients should be monitored for the emergence or worsening of depression, suicidal thoughts or behavior, and/or any unusual changes in mood or behavior. Discontinue Qsymia in patients who experience suicidal thoughts or behaviors. Qsymia is not recommended in patients with a history of suicidal attempts or active suicidal ideation.

      Acute angle closure glaucoma has been reported in patients treated with topiramate, a component of Qsymia. Symptoms include acute onset of decreased visual acuity and/or eye pain. Symptoms typically occur within 1 month of initiating treatment with topiramate but may occur at any time during therapy. The primary treatment to reverse symptoms is immediate discontinuation of Qsymia.

      Qsymia can cause mood disorders, including depression and anxiety, as well as insomnia. Qsymia can cause cognitive dysfunction (e.g., impairment of concentration/attention, difficulty with memory, and speech or language problems, particularly word-finding difficulties). Since Qsymia has the potential to impair cognitive function, patients should be cautioned about operating hazardous machinery, including automobiles.

      Hyperchloremic, non-anion gap, metabolic acidosis has been reported in patients treated with Qsymia. If metabolic acidosis develops and persists, consideration should be given to reducing the dose or discontinuing Qsymia.

      Qsymia can cause an increase in serum creatinine. If persistent elevations in creatinine occur while taking Qsymia, reduce the dose or discontinue Qsymia.

      Weight loss may increase the risk of hypoglycemia in patients with type 2 diabetes mellitus treated with insulin and/or insulin secretagogues (e.g., sulfonylureas). Qsymia has not been studied in combination with insulin. A reduction in the dose of antidiabetic medications which are non-glucose-dependent should be considered to mitigate the risk of hypoglycemia.

      The most commonly observed side effects in controlled clinical studies, 5% or greater and at least 1.5 times placebo, include paraesthesia, dizziness, dysgeusia, insomnia, constipation, and dry mouth.

      To report negative side effects, contact VIVUS, Inc. at 1-888-998-4887 or FDA at 1-800-FDA-1088

      Please read the Full Prescribing Information for Qsymia.

      Sentiment: Strong Sell

 
VVUS
2.79+0.02(+0.72%)Mar 3 4:00 PMEST

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