Finpecia a generic of Finasteride hair loss drug
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Generic Finasteride to Treat Hair Loss
Finpecia (Generic Finasteride) is for use by men only. Finpecia is used to treat men with male pattern hair loss to increase hair growth on the scalp and to prevent further hair loss. Male pattern hair loss (also known as androgenetic alopecia) is a common condition in which men experience thinning of the hair on the scalp. This often results in a receding hair line and/or balding on the top of the head. These changes typically start to occur in some men in their 20s and become more common with age. Once hair loss has occurred over a long period of time, the hair may be permanently lost. Male pattern hair loss is thought to be caused by a combination of family history (heredity) and production of a particular male hormone, called dihydrotestosterone (DHT). Men with male pattern hair loss have more DHT in the balding part of their scalp than in other parts, resulting in increased hair loss.
How Generic Finasteride (Finpecia) Treats Male Pattern Baldness
Finpecia specifically lowers the levels of DHT in the scalp, thus helping to reverse the balding process. Finpecia does not affect hair on other parts of the body. Men with mild to moderate, but not complete, hair loss can expect to benefit from the use of Finpecia. In women who were studied Finpecia was not effective in the treatment of hair loss (androgenetic alopecia) There should be no need to change your usual hair care routine (for example, shampooing or haircuts) because you are taking Finpecia. Finpecia is not addictive.
Do not take Finasteride if:
You have an allergy to Finpecia or any of the ingredients listed at the end of this leaflet Symptoms of an allergic reaction to Finpecia may include skin rash or swelling of the lips or face. The packaging is torn or shows signs of tampering The expiry date on the pack has passed If you take this medicine after the expiry date has passed, it may not work.
If you are not sure whether you should start taking Finasteride for hair loss, talk to your doctor. Women who are pregnant or may be pregnant must not take Finpecia (Finasteride), handle crushed or broken tablets or handle tablets with wet hands. If the active ingredient in Finpecia is absorbed after swallowing the tablet or through the skin by a woman who is pregnant with a male baby, it may cause the male baby to be born with abnormalities of the sex organs. Whole tablets are coated to prevent contact with the active ingredient during normal handling, provided that the tablets haven’t been crushed or broken. If a pregnant woman swallows Finasteride (Finpecia), handles crushed or broken tablets or handles tablets with wet hands, her doctor must be consulted immediately. Do not give Finpecia to children or women. Finpecia is for use by men only.
Top reasons to Order Generic Propecia
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In this article you will learn the exact steps to take to EFFECTIVELY stop your hair loss, and even experience regrowth.All you need to know to order propecia online.
To understand how to stop your hair loss it’s important to know what the root cause of it is…
The basic explanation is that DHT (the ageing hormone) results in the loss of hair because it destroys hair follicles. But the reason DHT is produced is very misunderstood.
The common misconception is that DHT is caused by too much testosterone in the body. This is wholly incorrect and proven to be so by the latest scientific findings from the last 10 years.
What has been found to be true is that is it excess estrogen -the female hormone- that causes the OVERproduction of DHT. In fact, too much estrogen in the body is being found as the root cause for many degenerative diseases and health conditions besides hair loss.
The simple fact is this: too much estrogen (called estrogen dominance) results in the massive production of DHT which overwhelms the body’s delicate hormone system and causes hair loss.
Once this is understood, stopping hair loss is relatively easy, and can be done in 3 simple steps.
1. Pollution in the environment is a major cause of production of estrogen. Car fumes and other pollutants need to be neutralized by the liver BEFORE they turn into estrogen. If the liver doesn’t do this effectively, estrogen will be produced…
But the liver is often underperforming due to many years of constant stress in dealing with these pollutants, and needs revitalizing. This can be done by taking a liver cleansing supplement.
2. Toxic chemicals are often put into modern food to help them last longer on supermarket shelves (preservatives) or taste better (flavorings). Unfortunately these cause the production of estrogen. For this reason it is best to eat organic food. Organic food has become very affordable in recent years and is well worth the extra pennies.
3. Once the above two steps are done, no more DHT will be produced and this is vital to stopping your hair loss. However, there still exists the small matter of existing DHT on the scalp, which will cause further hair loss until it is removed. This is simply done by using a DHT removing agent. Many expensive ones exist but to be honest you can use a homemade one to do the job just as effectively, and will cost you much less.
As you can see with this three steps you will get a lot of headaches with what to do when and how…the simple method to stop your hair loss is buying generic propecia ..no stress …just a pill from time to time and you’ll be again a hairy person 
Generic Propecia Online Medication
Posted by admin on Jan 17, 2008
How hair loss medication can inhibit DHT and Alopecia Areata
If you are going bald you should seriously consider hair loss medication treatments to halt or even reverse your hair loss. While there is no “Hair Loss Cure”, hair loss drugs like finasteride (Propecia) and dutasteride (Avodart) can often stop or even reverse alopecia areata in most people.
Studies have shown that 80% of men using Propecia stopped or even reversed their hair loss to some degree. Preliminary clinical trials for Avodart appear even more effective than Propecia.
However, neither Propecia nor Avodart has been proven to restore hair in the frontal areas. For reasons yet unknown these drugs, along with Rogaine, only generally work in regrowing thinning hair in crown area of the scalp. Only hair transplant surgery has been successful in restoring hair in the frontal hairline area once it has been lost.
Propecia and Avodart are also less effective in growing hair in older men. These hair loss drugs work best for men who have been balding for less than five years.
Women must NOT USE Propecia
Both Propecia and Avodart are not recommended for use by women or children.
It’s been found that these drugs can cause birth defects. More specifically, these birth defects may occur when large amounts of the drug are absorbed into the body during the period of fetal development.
Physicians advise pregnant women to not handle Propecia tablets, as this may harm male fetuses. But as of yet, there has not been a single reported case of birth defects caused by handling these tablets.
Furthermore, there’s also no evidence that pregnant women exposed to the semen of Propecia or Avodart patients will risk any birth defects.
Propecia and Avodart are also not advisable for men with liver disease or prostate cancer.
Get a Prescription for Propecia or Avodart.
Often our member physicians will prescribe Propecia or Avodart to halt a patient’s hair loss and then restore the hair already lost with hair transplant surgery. These treatments in combination can work synergistically. The drugs work to halt the hair loss, while hair restoration surgery restores what was lost.
To get a prescription for Propecia or Avodart schedule a free no obligation consultation with any of our quality hair restoration physicians. Find a physician in your area.
Propecia and Avodart should be taken once a day. It has been found that after two years of treatment, Propecia effectively grows hair in about 66% of patients. Also, about 83% of the subjects receiving this treatment continue to maintain their existing hair after two years.
Propecia (Finasteride) was originally a drug called Proscar, which was used to treat and reduce mens prostate conditions such as benign prostatic hyperplasia (BPH).
Its parent company, Merck & Co., soon realized that the drug had a unique side effect - it grew hair on bald men’s heads.
In December 22, 1997 the FDA approved Propecia as a hair loss pill. Merck & Co. then marketed the drug as a hair loss treatment under the trade name of Propecia.
More recently Dutasteride, sold as Avodart, has generated interest as a promising new hair loss medication. Like finasteride (Propecia) it inhibits the creation of DHT and was originally developed as a treatment for men’s prostate condition.
However, unlike Propecia, Avodart inhibits the creation of both type one and type two 5 alpha reductase enzymes. Dutasteride has been shown to decrease levels of DHT by 90% after only two weeks, making it a more powerful and faster acting weapon against hair loss than Propecia (Finasteride).
Dutasteride is not yet FDA approved for the treatment of hair loss. However, some hair restoration physicians also prescribe it for the treatment of hair loss. Like Propecia, Avodart is not safe for women and children.
Sticking with the program to see results
Loosing your hair took time. So too will regrowing your hair using Propecia or Avodart. These drugs require patients to take the drug daily for at least three months before any obvious changes will be noticeable. Most physicians advice taking these drugs for a year before evaluating their effectiveness.
At this time, Propecia and Avodart are only available by prescription. Our member physicians are available to discuss these hair loss drugs with you and prescribe them if appropriate. To find a quality hair restoration physician in your area.
Other DHT Blockers
Aside from Propecia and Dutasteride, there are other treatment options (all topical) that may or may not work to block the effects of DHT on vulnerable hair follicles. These include Revivogen, Crinagen, Progesterone Creams, and Xandrox (a type of minoxidil). Other DHT Blockers
To learn more about these treatments, as well as all other topical options, visit our Topical Hair Loss Products and Treatments section.
Purchase Credible Hair Loss Treatments Online
To learn more about these hair loss treatments or to purchase them online visit the Hair Loss Talk. This site has an excellent reputation online for reliable service and credible content.
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Stop Hair Loss with PROPECIA
When high levels of a naturally occurring hormone called DHT are present in the scalps of men
genetically disposed to Male Pattern Hair Loss, the growth phase of hair is shortened. Eventually,
the hairs become so small as to be practically invisible. This can result in the classic male bald
hairline if it is not stopped.
Generic Propecia NOW AVAILABLE
4rx now stocks Generic Propecia (Finpecia). Finpecia contains 1 mg Finasteride the same ingredient as in Propecia.
PROPECIA Reduces Levels of DHT
PROPECIA works by blocking the enzyme 5 alpha reductase. This reduces the level of hormone, DHT,
in the scalp and allows hairs to revert to a normal growth cycle. This results in no further hair
loss and significantly new hair growth in men with Male Pattern Hair Loss.
Propecia became the first anti-baldness pill approved by the FDA in 1997.
The active ingredient is finasteride 1mg.
Generic Propecia
Posted by admin on Jan 17, 2008
GENERIC PROPECIA
Integrated analysis of clinical adverse experiences showed that during treatment with PROPECIA, 36 (3.8%) of 945 men had reported one or more of these adverse experiences as compared to 20 (2.1%) of 934 men treated with placebo (p=0.04). Resolution occurred in men who discontinued therapy with PROPECIA due to these side effects and in most of those who continued therapy. The incidence of each of the above adverse experiences decreased to £0.3% by the fifth year of treatment with PROPECIA.
In a study of finasteride 1 mg daily in healthy men, a median decrease in ejaculate volume of 0.3 mL (-11%) compared with 0.2 mL (–8%) for placebo was observed after 48 weeks of treatment. Two other studies showed that finasteride at 5 times the dosage of PROPECIA (5 mg daily) produced significant median decreases of approximately 0.5 mL (-25%) compared to placebo in ejaculate volume, but this was reversible after discontinuation of treatment.
In the clinical studies with PROPECIA, the incidences for breast tenderness and enlargement, hypersensitivity reactions, and testicular pain in finasteride-treated patients were not different from those in patients treated with placebo.
Postmarketing Experience for PROPECIA (finasteride 1 mg)
Breast tenderness and enlargement; hypersensitivity reactions including rash, pruritus, urticaria, and swelling of the lips and face; and testicular pain. See Controlled Clinical Trials and Long-Term Open Extension Studies for PROSCAR* (finasteride 5 mg) in the Treatment of Benign Prostatic Hyperplasia.
Controlled Clinical Trials and Long-Term Open Extension Studies for PROSCAR* (finasteride 5 mg) in the Treatment of Benign Prostatic Hyperplasia
In the PROSCAR Long-Term Efficacy and Safety Study (PLESS), a 4-year controlled clinical study, 3040 patients between the ages of 45 and 78 with symptomatic BPH and an enlarged prostate were evaluated for safety over a period of 4 years (1524 on PROSCAR 5 mg/day and 1516 on placebo). 3.7% (57 patients) treated with PROSCAR 5 mg and 2.1% (32 patients) treated with placebo discontinued therapy as a result of adverse reactions related to sexual function, which are the most frequently reported adverse reactions.
Table 2 presents the only clinical adverse reactions considered possibly, probably or definitely drug related by the investigator, for which the incidence on PROSCAR was ³1% and greater than placebo over the 4 years of the study. In years 2-4 of the study, there was no significant difference between treatment groups in the incidences of impotence, decreased libido and ejaculation disorder.
The adverse experience profiles in the 1-year, placebo-controlled, Phase III BPH studies and the 5-year open extensions with PROSCAR 5 mg and PLESS were similar.
There is no evidence of increased adverse experiences with increased duration of treatment with PROSCAR 5 mg. New reports of drug-related sexual adverse experiences decreased with duration of therapy.
The relationship between long-term use of finasteride and male breast neoplasia is currently unknown. During a 4- to 6-year placebo- and comparator-controlled study that enrolled 3047 men, there were 4 cases of breast cancer in men treated with PROSCAR but no cases in men not treated with PROSCAR. In another 4-year, placebo-controlled study that enrolled 3040 men, there were 2 cases of breast cancer in placebo-treated men, but no cases were reported in men treated with PROSCAR.
In a 7-year placebo-controlled trial that enrolled 18,882 healthy men, 9060 had prostate needle biopsy data available for analysis. In the PROSCAR group, 280 (6.4%) men had prostate cancer with Gleason scores of 7-10 detected on needle biopsy vs. 237 (5.1%) men in the placebo group. Of the total cases of prostate cancer diagnosed in this study, approximately 98% were classified as intracapsular (stage T1 or T2). The clinical significance of these findings is unknown. This information from the literature (Thompson IM, Goodman PJ, Tangen CM, et al. The influence of finasteride on the development of prostate cancer. N Engl J Med 2003;349:213-22) is provided for consideration by physicians when PROSCAR is used as indicated. PROSCAR is not approved to reduce the risk of developing prostate cancer.
DRUG INTERACTIONS
No drug interactions of clinical importance have been identified. Finasteride does not appear to affect the cytochrome P450-linked drug-metabolizing enzyme system. Compounds that have been tested in man include antipyrine, digoxin, propranolol, theophylline, and warfarin and no clinically meaningful interactions were found.
Other concomitant therapy
Although specific interaction studies were not performed, finasteride doses of 1 mg or more were concomitantly used in clinical studies with acetaminophen, acetylsalicylic acid, a-blockers, analgesics, angiotensin-converting enzyme (ACE) inhibitors, anticonvulsants, benzodiazepines, beta blockers, calcium-channel blockers, cardiac nitrates, diuretics, H2 antagonists, HMG-CoA reductase inhibitors, prostaglandin synthetase inhibitors (also referred to as NSAIDs), and quinolone anti-infectives without evidence of clinically significant adverse interactions.
Drug/Laboratory Test Interactions
Finasteride had no effect on circulating levels of cortisol, thyroid-stimulating hormone, or thyroxine, nor did it affect the plasma lipid profile (e.g., total cholesterol, low-density lipoproteins, high-density lipoproteins and triglycerides) or bone mineral density. In studies with finasteride, no clinically meaningful changes in luteinizing hormone (LH), follicle-stimulating hormone (FSH) or prolactin were detected. In healthy volunteers, treatment with finasteride did not alter the response of LH and FSH to gonadotropin-releasing hormone indicating that the hypothalamic-pituitary-testicular axis was not affected.
In clinical studies with PROPECIA (finasteride, 1 mg) in men 18-41 years of age, the mean value of serum prostate-specific antigen (PSA) decreased from 0.7 ng/mL at baseline to 0.5 ng/mL at Month 12. Further, in clinical studies with PROSCAR (finasteride, 5 mg) when used in older men who have benign prostatic hyperplasia (BPH), PSA levels are decreased by approximately 50%. These findings should be taken into account for proper interpretation of serum PSA when evaluating men treated with finasteride.