Showing posts with label FDA. Show all posts
Showing posts with label FDA. Show all posts

Wednesday, October 30, 2013

Hepatitis C drug Gilead's sofosbuvir to get FDA Approval

Check out the positive review of Gilead Sciences Inc's hepatitis C drug - Sofosbuvir given by the ‘U.S. Food and Drug Administration’ (FDA).

Gilead Sciences’ much-anticipated hepatitis C drug, named as Sofosbuvir, has been given the thumbs up by an FDA advisory group. All 15 members of the Food and Drug Administration’s panel of virus experts have voted in favor of approving Sofosbuvir, a daily pill designed to treat several forms of Hepatitis C. Usually FDA follows the recommendations made by its advisory panels, but not required to do so. The FDA is expected to make the final decision regarding the approval of the drug by 8th of December 2013.

Hepatitis C drug Gilead's sofosbuvir

Friday, June 21, 2013

PlanB one-step is now approved by FDA

Millions of women take birth control or contraception pills to prevent unplanned pregnancy after an unprotected sex. This backup method is safe, convenient and effective way to avoid unnecessary pregnancy when a regular birth control method fails or used wrongly. Every year, nearly 2 million unplanned pregnancies are prevented with the help of publicly funded contraception in the United States. Recently, FDA has approved Plan B one-step progestin-only emergency contraceptive pill as a nonprescription product that means it is going to be sold over-the-counter for all women without age restrictions.

PlanB one-step is now approved by FDA

Since July 2009, Plan B one-step was already approved by FDA as a nonprescription product for women age 17 years or above. In 2011, the FDA was planning to allow emergency contraceptives as a nonprescription product without age restrictions but Kathleen Sebelius (Health and Human Services Secretary) overruled her own scientists in an extraordinary move. In April 2013, Edward Korman (U.S. District Judge) ordered the FDA to approve emergency contraceptive for all women with child-bearing potential without any prescription. Due to this approval, PlanB one-step emergency contraceptive age limit has been decreased to 15 years.

The Plan B One-Step is a single-dose emergency contraceptive that cut the chances of being pregnant by 89% if taken within 72 hours (3 days) of unprotected sexual intercourse, rape or condom failure. It works best if taken within the first twenty-four hours. The pill does not work if girl or woman is already pregnant.
The active ingredient of pill is levonorgestrel, the same ingredient found in many birth control pills. The pill works just like other birth control pills. It prevents ovulation (the release of an egg from the ovary) or fertilization (joining of an egg cell and a sperm cell) and thus, avoids pregnancy. The pills are available at the retail pharmacy stores.

The pill is not as effective as regular birth control pills so don’t consume it regularly. Common side effects of pill are changes in period, breast tenderness, nausea, headache, dizziness, fatigue and lower abdominal pain. It will not protect a woman from HIV infection or STDs (sexually transmitted diseases). Women who are allergic to levonorgestrel should not take Plan B One-Step.

At present, three types of emergency contraceptive are available in the U.S. such as ella, Plan B and One-Step. Ella is prescription-only product while Plan B is available as OTC product for women aged 17 and above.

Friday, July 6, 2012

OraQuick: FDA approved HIV test for quick & home AIDS diagnosis

For the treatment of any disease whether it is a major disease or a minor one, the most important thing is its diagnosis. Without diagnosis, we cannot think about the treatment, as before that we must know what the problem actually is. Technology has made everything so easy for us that we can diagnose many disorders and problems sitting at our home. It may be a minor fever to a major, blood pressure or diabetes. Many Pregnancy test kits are also available that confirm whether a woman is pregnant or not without visiting the doctor. However, it is important to visit the doctor for a confirmed diagnosis or treatment. But when it comes to a sexual disease, many people hesitate to visit the doctor. AIDS is also an STD in which no cure has been found yet. Also, there are many misconceptions related to this disease. So generally when people come to know that a particular person is HIV positive, they tend to avoid that person. This is one more reason people try to avoid the doctor to get their disease diagnosed. But now the time and situation both have been changed. OraQuick In-Home HIV Test is here to help these people, who do not want to go out of their home to get their disease diagnosed. Using OraQuick test kit anyone can check whether he/she is HIV positive or not, right at home.
OraQuick: FDA approved HIV test for quick & home AIDS diagnosis

Saturday, June 30, 2012

Belviq is FDA approved anti-obesity pill

The first innovative prescription drug for long-term weight loss, Arena Pharmaceutical's anti-obesity pill Belviq has been approved on Wednesday by the Food and Drug Administration. Belviq becomes the first federal-approved prescription drug for weight loss in 13 years and is expected to enter the U.S. market in the next decade. This drug got approval from FDA so it seems to be safe enough and called as a new weight-loss treatment by doctors. This pill is for adults, who are overweight or are obese and have at least one medical complication, like high cholesterol or diabetes.

Belviq is FDA approved anti-obesity pill

Friday, May 11, 2012

Truvada: A first HIV Prevention pill in queue for FDA approval

Truvada, a pill already approved to treat the HIV infected people since 2004, is expected to move one step further to get the approval for becoming the first official HIV Prevention pill to thwart healthy people from being infected with AIDS causing virus. An advisory panel of experts recently suggested the Food and Drug Administration (FDA) agency that the daily pill Truvada should be made official for preventing the deadly disease in healthy people who are at high risk of HIV contagion. It is the very first time that government advisory committee have suggested to give antiviral medicine to healthy people who are at a risk of exposure to HIV virus through the sexual activity.

Truvada: A first HIV Prevention pill in queue for FDA approval

The Antiviral Drugs Advisory Committee of FDA suggested the approval of pre-exposure prophylaxis (PrEP) drug for the healthy people of three groups: 1) men who have sex with men (gay), 2) heterosexual couples with one HIV-positive partner, and 3) bisexual men. The risk-benefit analysis favored approval of the drug for the people of first group with the strongest yes vote of 19-3 from the Advisory Committee. The Committee voted 19-2 with 1 abstention for the second group and 12-8 with 2 abstentions for the third group, favoring approval for both the groups. The FDA is not required to pursue the suggestions of the advisory committees made up of experts from outside the agency, but it pursues usually.
An ultimate decision for the approval by FDA is anticipated by June 15. If the FDA will give the approval for once-a-day HIV prevention pill, it would be the turning point for the thirty-year combat against a contagion which causes 2.7 million new HIV diseases globally every year, as stated by the United Nations Program on HIV/AIDS.

FDA has already approved this drug in 2004 for the treatment of HIV infections. Therefore, the physicians can prescribe Truvada "off label" for HIV prevention. It has been already utilized ''off-label" as a precautionary drug by high-risk people like man who has sex with man. But, if the FDA will give approval of Truvada as a preventive drug, then the manufacturer company of the drug - Gilead Sciences - would be able to trade the drug for prevention freely.

Prevention & risk reduction
A three-year study presented to the Antiviral Drugs Advisory Committee of FDA reveals that Truvada cuts the risk of acquiring HIV by 42% in healthy bisexual men and gay, when accompanied with counseling and condoms. One other study shows that Truvada cuts the risk of infection by 75% among heterosexual couples, where one partner was HIV-positive and the other was not. These rates of prevention would have been superior if all the participants take the drug every day as directed, the representatives of Gilead told the committee.

Blood tests of the participants showed that majority of them didn’t take the pills on a regular basis, in spite of their involvement in studies which included regular visits with health-care providers. The prevention rates were beyond 90% in the participants, who took the drug regularly.

Truvada is not destined to substitute condoms and other sex-safety measures, but to be utilized with them for further protection.

Why better prevention is required?

Roughly 50,000 new HIV infections occur in the United States every year, that’s why the better methods of prevention are required. Several speakers put emphasis on the fact that the cases of AIDS occurrence has not budged in 15-20 years. That clearly means, the condoms and counseling are not doing much good. Moreover, the sexual partners of many of the newly infected people do not realize that they are HIV-positive.

According to the Centers for Disease Control and Prevention (CDC), men who have sex with men keep on embracing most new infections and the ratio of new infections occurrence in this group raised from 55 % to 61 % from 2007 to 2010. The risk of HIV virus contagion is higher in young black men who have sex with men. According to the CDC, Hispanics and Blacks have a higher risk of deadly disease than whites.
Some members of the advisory committee worried about the risk that people who got HIV contagion while taking Truvada might develop hazardous drug-resistant strains of the virus. However, the committee decided that the advantages of infection prevention prevailed over the risks. There is no word whether the drug will be effective in preventing the HIV infection spread by needle sharing or not. Some committee member alleged that there is not an enough data to provide evidence for the safety and affectivity of drug in African Americans or women.

The approval of FDA would aid to ensure that pills are being utilized more safely and effectively, according to the recommenders of Truvada as a preventive drug. The pills would have to be marked with specific instructions such as which lab tests are necessary for patients for safety reasons. For example, the test for the HIV infection must be done before starting the drug, the reason is that drug-resistant strains of the virus may rapidly develop if the Truvada is taken alone by an HIV-infected patient. Some patients may also require for testifying their kidney function. Truvada even can lead to slight decline in bone density, which may need monitoring.

The approval of FDA may make it more probable that precautionary use of the drug would be covered by insurance that costs around $14,000 a year.

About Truvada

Truvada is composed of two antiviral drugs: Emtriva and Viread. This drug is being used alone for pre-exposure prophylaxis, but it must be used along with other antivirals for the treatment of HIV. It works by aiding to block a chemical in the body, which requires for the multiplication of HIV.
After the approval of Truvada in 2004, it swiftly became one of the top-vending HIV drugs. The expenditure of the drug is around $1,100 per month.
The senior vice president of company at the Foster City, Calif., Andrew Cheng said that the drug should be included to the "existing toolbox" of prevention techniques, including education about clean-needle programs, condom use and safe sex.

Thursday, April 14, 2011

The effectiveness of Morning-after Pills in Emergency Contraception

The “Morning-after pill” is safe and effective way for birth control which prevents the pregnancy after unprotected sexual intercourse. This pill decreases the possibilities of being pregnant but on the other side it does not induce abortion. The morning-after pill possesses hormone levonorgestrel, progestin (Plan B One-Step, Next Choice) or progesterone agonist-antagonist, ulipristal acetate (Ella) is more efficient than the combined emergency contraceptive pill.

The effectiveness of Morning-after Pills in Emergency Contraception


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