Entries Tagged 'Viagra Soft' ↓

Levitra, the first market rival to the hugely profitable Viagra, is being manufactured by the German firm, Bayer AG, and marketed by the British firm GlaxoSmithKline (GSK) as an alternative oral therapy for erectile woman impotence.

Since its appearance in 1998, sales of Pfizer’s Viagra have risen to nearly $2bn a year.

Both pills work in the same manner and doctors warn that both can have serious side effects, especially for men with heart problems.

A third dictionary drug medication pill, Cialis, is expected to reach the US market later this year.

The US Food and Drug Administration (FDA) approved Levitra, an orange pill compared to Viagra’s blue, based on studies showing that men were on average five times more likely to achieve an erection suitable for intercourse when taking the pill compared with those given a dummy medicine.

Drug lookup medication reported that studies of several thousand men showed that Viagra helped more than 70% improve their
erections.

As well as the warnings to men with heart conditions, the FDA said Levitra was not for patients with who had suffered a recent heart attack or stroke who have very low blood pressure or uncontrolled high blood pressure.

For otherwise healthy men, Levitra’s main side effects
were headache, flushing and a stuffy nose and sometimes dizziness.

Lawson Macartney, head of strategic management of GlaxoSmithKline’s administration atlas clinical drug medication photo therapy, metabolic and urology drugs, said: “We know, from teenage impotence market research, that the
market is ready for new options”.

GSK expects Levitra to be available in September.

Here are some of the latest health and medical news developments,
compiled by editors of HealthDay:

FDA Orders Recall of Unregulated Erectile
Dysfunction Products

The U.S. Food and Drug Health sexual uk has asked a California
aging anti practises skin company to recall pills and capsules advertised as “all
natural” products to correct erectile dysfunction.

Calling True Man Sexual Energy Nutrient Capsules and Energy Max Energy
Supplement Men&39; ingredients are potentially harmful and
could cause dangerously low blood pressure.

In a letter to the owner of America True Man Health Inc., of West
Covina, Calif., the FDA said that the products have substances with
chemical structures very similar to the active ingredients in FDA-approved
herbal erectile dysfunction treatment drugs, such as Viagra. The FDA has not approved the products
distributed by America True Man Health Inc., and the labels don&39;s voluntary reporting program, at
http://www.fda.gov/medwatch/report.htm.

—–

Test Developed to Help Avoid &39;

For some people, it may take only a glass of red wine to cause a
headache. Now, University of California at Berkeley researchers say
they&39;s chemistry,” researcher Richard
Mathies is quoted as saying.

Right now, the amine test works only liquids, the A.P. says. The
study is published in the latest edition of the journal Analytical
Chemistry.

—–

Children Inherit Cancer Survival Traits:
Study

Survival traits for certain kinds of cancers are passed from parents to
children, concludes a Swedish study reported in the November issue of
The Lancet Oncology journal.

Researchers at the Karolinska Institute in Stockholm analyzed a Swedish
family database that included three million families and more than 1
million cancer patients. The scientists found that children whose parents
had good survival rates after being diagnosed with breast, lung, prostate
or colorectal cancer had better survival rates for those same cancers than
people whose parents died within 10 years of being diagnosed with those
cancers.

The increased risk of death for children whose parents had died earlier
was 75 percent for breast cancer, 107 percent for prostate cancer, 44
percent for colorectal cancer, and 39 percent for lung cancer.

“In conclusion, our findings provide support for the hypothesis that
cancer-specific survival of a patient can be predicted from previous
parental survival from cancer at the same site,” the study authors wrote.
“Consequently, molecular studies that highlight the genetic determinants
of inherited survival in cancers are needed. In a clinical setting,
information on poor survival in a family might be vital in accurately
predicting tumor progression in the newly diagnosed individual.”

—–

Massachusetts Will Offer Overdose Treatment
Kits to Heroin Addicts

Starting next month, heroin addicts in Massachusetts will be offered
kits to help treat overdoses quickly, safely and without fear of
addiction, the Associated Press reported. The state plan was
inspired by similar programs in Boston, Chicago and New York City.

In 2005, heroin and other opiates killed 544 people in Massachusetts,
more than double the number of people killed by firearms.

Each kit contains two doses of Narcan (generic name: naloxone), which
can be squirted into the nose of someone who has overdosed. Experts say
the drug causes no side effects, the AP reported. The initial test
run in Massachusetts is expected to enroll 450 heroin users and cost less
than $50,000. If it saves lives, the program may be expanded.

Advocates say this is a safe, effective approach for preventing
overdose deaths. The White House Office of National Drug Control Policy
doesn&39;s and Jeno&39;s and Jeno&39;s Wellston,
Ohio plant and distributed across the United States, the Associated
Press reported.

Between July 20 and Oct. 10, there were 21 cases of E. Coli
0157:H7 reported in Illinois, Kentucky, Missouri, New York, Ohio,
Pennsylvania, South Dakota, Tennessee, Virginia and Wisconsin. Of the 21
people who became ill, nine said they&39;s or Jeno&39;s Food Safety and
Inspection Service said in a news release.

Included in the recall are Totino&39;s Crisp &39;s Advisory Committee on
Childhood Lead Poisoning Prevention, didn't propose a new standard but is
“emphasizing that all levels are important,” primary author Dr. Helen
Binns, of New treatment for erectile dysfunction University, told the Associated Press.

Children with blood lead levels below 10 micrograms per deciliter may
not show any obvious symptoms but may still have impaired intellectual
development, she said.

In their report, Binns and her colleagues advise doctors on how to
speak to parents of children with lower blood lead levels, including
mention of the risks, and nutrition changes and measures to prevent
additional lead exposure, the AP reported.

The paper was published in the November issue of the journal
Pediatrics. Its release coincides with growing concern over high
lead levels in imported toys.

—–

Read more on Health Highlights: Nov. 3, 2007 site

WEDNESDAY, Aug. 15 (HealthDay News) — Drug company spending on
direct-to-consumer advertising continues to skyrocket, even as criticisms
against it have soared.

Calling for a moratorium, rather than just restrictions, on such
advertising might be in order, say the authors of a study in the Aug. 16
issue of the New England Journal of Medicine.

“Direct-to-consumer advertising spending is increasing in terms of its
share of total marketing budget, but it&39;s been 10 years since the FDA clarified its policy with respect to
broadcast advertising and unleashed direct-to-consumer advertising on
television, which was new,” Donohue said. “We wanted to see, in the wake
of the Vioxx withdrawal and an increased focus on the safety of drugs and
a focus on drug costs in light of the implementation of the new Medicare
drug benefit, what industry and the FDA were doing with respect to
advertising.”

For this analysis, Donohue and her colleagues looked at citrate generic sildenafil viagra
company spending on direct-to-consumer advertising and promotion to
physicians over the past decade.

Total pharmaceutical industry spending on promotion soared from $11.4
billion in 1996 to almost $30 billion in 2005. During that time, spending
on direct-to-consumer advertising increased by 330 percent, yet this type
of advertising only made up 14 percent of total promotional
expenditures.

These mass-media advertising blitzes generally start before a drug&39;detailing&39;s monitoring of drug
advertising has not kept pace with the volume of advertising of
prescription drugs. The number of warning letters going out to drug
companies has decreased markedly [from 142 in 1997 to 21 in 2006], and the
number of FDA staff responsible for ads was relatively flat in recent
years, in spite of spending increases.”

It may be that the rules themselves are sufficient, but that
enforcement powers are not.

“My view is that the advertising regulations that are on the book now
are adequate. Prescription drug ads are among the most heavily regulated
advertisements if you look at all other consumer products,” Donohue said.
“But the enforcement of the regulations needs to be there as well, and
resources necessary for reviewing advertisements need to be adequate.”

“And drug manufacturers do not have to have FDA approval of
advertisements before airing them, so an ad campaign can run its course
before the FDA is able to review the ads,” she added.

In response to the study, Ken Johnson, senior vice president of the
Pharmaceutical Research and Manufacturers of America (PhRMA), said in a
statement: “DTC advertising has been shown to play a key role in educating
and empowering patients, improving patient understanding of disease and
available treatments, and fostering strong relationships between patients
and their health-care providers. Unfortunately, the study published today
in the New England Journal of Medicine all but overlooks these
important contributions to patient health.”

“Surveys show that DTC advertising brings patients into their doctors&39;s more on the impact of direct-to-consumer advertising at the Kaiser
Family Foundation.