Daunting information about Suprenza

Diet pills are an easy way to lose weight. People no longer have the time to stick to a good and healthy diet or exercise for losing weight. And so, they resort to diet pills. But not all diet pills work miracles; some of them just come with loads of side effects.

Even the most effective of the pills should be used for only a very short period and only after consultation with a doctor. Also, in order for the diet pill to work, you need to support it with a healthy diet and exercise. Bad diet pills often cause side effects such as stomach cramping, diarrhea, gas, increased blood pressure and in some cases, cardiac arrest.

Suprenza is one such diet pill that promised to reduce weight by burning fat. It is unknown as to how the pill will help you lose weight. It may decrease your appetite, increase your body’s energy or affect some hormones. But, the known fact is that Suprenza suppresses the appetite.

• General Information – Suprenza is an orally disintegrating diet tablet that is used for losing weight. It contains Phentermine, a Schedule IV controlled substance. It is used as a therapy for management of obesity. The brain contains points that control the appetite. When the patient takes Suprenza, certain chemicals are released that work as appetite suppressant.

• Ingredients – Suprenza contains the following ingredients –

 Active Ingredient

o Phentermine Hydrochloride, USP – Phentermine is a sympathomimetic amine anorectic

 Inactive Ingredients

o Mannitol Powder
o Powdered Citric Acid
o Povidone CL
o Sucralose
o Povidone K 30
o Magnesium Stearate
o Mannitol Preganulated,
o Soldium Lauryl Sulfate

• Brand Name Variations – Suprenza is the brand name of phentermine, similar to amphetamine. It affects the central nervous system and suppresses the appetite.

• Mechanism of Action – When a person, wishing to lose weight, uses Suprenza, Phentermine, the active ingredient in the diet pill affects the central nervous system and suppresses the appetite. This reduced appetite leads to lesser consumption of calories, decreasing weight. The body then uses the stored fat for energy and burns it.

• Dosing and Administration – The dosage is prescribed by the physician according to individual needs. However, manufacturer directions recommend a single 15 mg or 30 mg tablet to be placed on the tongue. The tablet will dissolve. Manufacturer also recommends avoiding administration of the tablet late evening.

• Adverse Effects – There are potential harmful side effects of using Suprenza. Some of these include the following –

o The high blood pressure in the pulmonary arties can result in breathlessness and result in death. Sometimes, lung transplantation is essential when the patient is not responsive to any of the available treatments.
o Valvular Heart Problem
o Withdrawal effects after using the drug for a long period
o Cardiovascular problems such as palpitation, high blood pressure, tachycardia and ischemic events
o Problems of Central nervous system such as overstimulation and restlessness, euphoria, insomnia, headache, tremor, dysphoria and psychosis
o Gastrointestinal problems such as unpleasant taste and dryness in the mouth, constipation, diarrhea and others
o Allergic reactions such as urticarial
o Endocrinal problems such as changes in the libido and impotence

The following side effects have also been observed in patients using Suprenza –

o Breathlessness
o Swelling of lower legs and feet
o Weakness
o Trouble in walking, speaking and thinking
o Trembling of hands and legs
o Chest pain
o Decreased mobility
o Racing or irregular pulse and heartbeat
o Headache
o Fainting

The user may also find skin rashes, itching and hives and welts in the skin indicating allergic reaction among others.

In rare cases, patients have also reported psychotic episodes.

Suprenza is available as 15mg and 30mg tablets. It is stored at room temperature. Patients suffering from diseases such as glaucoma, hypothyroidism, hypertension, having a history of drug abuse and others should avoid using Suprenza.

If you are looking for a way to lose weight, then consult your dietician and your doctor, who will put you on a healthy diet and an exercise regimen after considering your medical history. Even if you do wish to take the help of diet pills, make sure you know how the pill works before you decide to invest in it.

 

Find out if Diethylpropion will be effective for your weight loss goals

General Information
Diethylpropion is a prescription appetite suppressant that is considered potentially habit forming. It is regarded as a schedule IV controlled substance in the US and a class C drug in the UK. It is not recommended for use in anyone under age 16 but it is used in low doses for some patients aged 65 and older.

As with all members of the sympathomimetic amine anorectic drug class, diethylpropion stimulates the body’s stress response system in order to decrease appetite. When any drug in this category is prescribed as a weight loss aide, it is intended only to act as a supplement to diet and exercise for those who struggle with obesity.

Ingredients
The active ingredient in diethylpropion tablets is diethylpropion hydrochloride, whose chemical name is diethylpropion hydrochloride is 1-phenyl-2-diethylamino-1-propanone hydrochloride or hcl. It is a sympathetomimetic agent, meaning that it is similar to amphetamines in both chemical structure and action.

Brand Name Variations
Diethylpropion is also known as amfepramone and is sold under the generic name diethylpropion hydrochloride. It is currently available as several brand names including Anorex, Linea, Nobesine, Prefamone, Regenon, Tenuate and Tenuate Dospan. It was also available as Tepanil but this brand has been discontinued.

Mechanism of Action
Diethylpropion functions as a prodrug, requiring metabolism by the body in order to form the active drug known as ethcathinone. This stimulates the release of the neurotransmitter norepinephrine, leading to its characteristic spectrum of neurologically mediated activity. As this drug targets monoamine transporters, diethylpropion may cause interactions with other drugs also aimed at these same targets such as certain antidepressants.

Dosing and Administration
Diethylpropion is available as orally administered tablets in both short-acting and extended release formulations. The standard formulation is one 25 mg tablet taken orally three times daily, one hour before meals. The extended-release form is only taken once daily, as a single 75 mg tablet. Diethylpropion is recommended for only short-durations of use, in the range of 12 weeks or less.

History
Diethylpropion was first approved for use as a diet aide in the United States in 1959 but has never been a popular there or abroad. It was originally marketed as an effective weight loss aide free from side effects. By 1967, however, studies had shown that only single dose administration was associated with a lower occurrence of side effects and that its use over the weeks required to attain weight loss showed side effect rates at least as high as other sympathomimetics.

Adverse Effects
Diethylpropion is a stimulant and brings along with it the host of uncomfortable and often dangerous side effects associated with this class of drugs. While the unadvised use of excess pills or changes in dosing may be associated with an increased risk of side effects, any or all of these unintended outcomes may arise from use of diethylpropion even at prescribed doses.

Diethylpropion stimulates the heart, which can cause a sense of palpitations or rapid heart beat. If this effect is sufficiently strong or occurs in the presence of any existing heart problems, this can lead to the chest pain associated with lack of sufficient blood flow to the working heart muscle. The effect is similar to that experienced during a heart attack, the most frequent cause of death in stimulant drug overdose.

Other unpleasant side effects that may arise with the use of diethylpropion include anxiety, restlessness, dizziness, nausea, dry mouth, bizarre tastes in the mouth and an increased frequency of urination. More worrisome effects are those that require immediate medical attention such as blurred vision, chills, sore throat, fever, painful urination, skin rash, itching and any symptom related to the heart. In addition to palpiatations and chest pain, some other symptoms that may be due to effects on the heart include swelling of the feet or ankles and difficulty breathing.

This drug is not safe to use for anyone with a history of high blood pressure, heart disease, an irregular heartbeat, kidney problems, a history of seizures or allergies to foods or other substances. It is also not recommended for use in anyone who has used another diet aide within the prior 12 months or who takes any other diet aides such as herbal supplements.

 

Didrex – side effects galore

With all of the many methods for losing weight available, it is imperative for anyone who wishes to lose weight to sort out the methods that do not work from the methods that do. An example of a weight loss supplement that does not live up to its hype is Didrex (benzphetamine)

History
Didrex is a weight loss supplement (it is used for other things as well) that suppresses feelings of hunger in order to achieve weight loss.

General information
This weight loss supplement effects the nervous system. Doctors will urge you not to share any of your medication because of the fact that Didrex has been found to be addictive in individuals with previous drug addictions. This medication should not be taken if you are allergic to any of its ingredients. It is best to obtain all of your general information about this drug from a physician.

Ingredients
The ingredients of this medication include the following: Benzphetamine hydrochloride, calcium stearate, corn starch, erythrosine sodium. FD & C yellow no. 6, lactose, povidone, and sorbitol.

Brand name variations
When it is not called by its brand name Didrex, it is most commonly known as benzphetamine.

Mechanism of Action
Didrex’s mechanism of action is not fully known. For the most part, all that is understood about this medication is that it works much like an amphetamine does. Amphetamines decrease one’s appetite by releasing norepinephrine and/or dopamine in the brain.

Dosing and Administration
Dosage will depend on the way Didrex effects the body. The dosage starts at about 25mg to 50mg once a day a day; dosage is increased (to 25 to 50 milligrams one to three times a day) and decreased as needed by a physician. When a patient first begins using this weight loss supplement, it is usually taken whenever the patient would normally eat their first meal of the day. This medication is taken orally and can be taken with or without food.

Adverse Effects
Because of the way this medication effects the body, Didrex can cause your heart rate and pulse to rise to dangerously high levels. Aside from this, there are many other side effects of this medication that you should be aware of before deciding whether or not to use it as a part of your weight loss regimen. Just a few of several side effects that commonly occur include the following: convulsions (seizures), hallucinations, numbness or tingling in the arms and legs, trouble thinking, speaking, or walking, mood/mental changes, shakiness in the arms, legs, and feet, as well as several other harmful side effects. These are just the way this medication will effect your mood and the outside of your body.

This medication is capable of wreaking total havoc on the inside of your body as well. Healthcare professionals are reminded not only to look for serious physical side effects that one can see, but side effects that might occur inside the body as well. Tachycardia (rapid heart rate), elevation of blood pressure, and even isolated cases of cardiomyopathy (chronic disease of the heart muscle) and ischemic cardiac events have been reported in users of this deplorable weight loss supplement.

Although it is obvious from the evidence discussed here that the results of taking this weight loss supplement can be hazardous to your physical health, it can also effect your mental well being as well. Didrex has many other side effects that potential users of this drug should be aware of that are not mentioned here. Because of the harm that this drug can do to its user, it is horrifying to consider what this drug could potentially do to an unborn child. Therefore, it would be a serious mistake to consume this harmful drug.

 

Desoxyn – ineffectiveness and side effects

General Information
Desoxyn is the trade name for methamphetamine hydrochloride, a stimulant drug that is sometimes prescribed as a treatment for Attention Deficit Hyperactivity Disorder (ADHD) in children above the age of six. Desoxyn can also be prescribed to obese patients as a weight loss drug due to its appetite-reducing effects. The drug can also be used off-label as a treatment for narcolepsy or treatment-resistant depression.

Ingredients

The active ingredient in Desoxyn is methamphetamine hydrochloride. Inactive ingredients such as corn starch, lactose, stearic acid, talc and sodium paraminobenzoate are added to lend stability to the tablet’s structure.

Brand Name Variations

Desoxyn is sometimes known by different names, such as Syndrox, Methedrine, Pervitin, Anadrex, or Desoxyephedrine.

Mechanism of Action
Desoxyn works by affecting chemicals and neurotransmitters in the the brain that are believed to be responsible for both impulse control and hyperactivity.

Dosing and Administration
Desoxyn is administered orally via a tablet. A common dose for children is 5mg one to two times a day. In obese patients, the recommended dose is one 5mg tablet 30 minutes before a meal, with the overall daily dosage not exceeding 20-25mg.

Adverse Effects
Desoxyn has a number of side effects. It is highly addictive and is listed as a Schedule II drug. Desoxyn users have reported eyesight changes, seizures, insomnia, dry mouth, loss of appetite, accelerated heartbeat, tremors, constipation, diarrhea and nausea. The drug can also cause dry or itchy skin, rapid breathing, and bruxism. In children, Desoxyn can cause delayed growth. In some cases, the drug can lead to depression, psychosis, heart attacks, and strokes. Prolonged use of Desoxyn increases the chances that these side effects will be experienced by the user.

If you have a history of mental illness, a history of drug abuse, issues with glaucoma, high blood pressure, hyperthyroidism, epilepsy, a family history of heart failure or artery problems, or you have recently been taking monoamine oxidase inhibitor (MAOI) anti-depressant medications, then your doctor will most likely refuse to prescribe Desoxyn to you. If you are taking Desoxyn and begin to notice adverse side effects such as paranoia or hearing and seeing things that are not real, you should discontinue usage and talk to your doctor immediately.

Taking Desoxyn without understanding its effects can lead to addiction and even death. Because of these adverse effects, it is important that anyone who is taking Desoxyn does so under the close guidance of a medical professional.

Abuse and Possible Consequences
Because of Desoxyn’s use by certain groups of obese patients as a means to losing weight, many people have attempted to obtain the drug without a prescription in order to use it as a weight loss supplement. This is typically accomplished through illegal means such as buying the drug off a user with a valid prescription. This is an incredibly unsafe practice that can be detrimental to the health of the user. The risks that are associated with using Desoxyn without the guidance of a doctor far outweigh any potential benefits. Even if a person has been approved by your doctor to take Desoxyn as a weight loss aid, the side effects that it can cause means that Desoxyn should be seen as a last resort.

 

Do the side effects of Bontril PDM / SR outweigh the potential benefits?

General Information
Bontril PDM / SR is a sympathomimetic central nervous system stimulant and diet pill similar to amphetamine that is used as a short-term diet aide in addition to diet and exercise for individuals struggling with obesity aged 12 years and older. It is classified as a schedule III controlled substance in the United States.

Ingredients
The active ingredient in Bontril PDM / SR is phendimetrazine tartrate. Its chemical name is (2S,3S)-3,4-Dimethyl-2-phenylmorpholine L-(+)-tartrate (1:1). It is a member of the morpholine class of stimulant chemicals.

Brand Name Variations
The generic equivalent of Bontril PDM / SR is phendimetrazine. This is also available under the trade names Bontril, Melfiat, Obezine, Phendiet, Phendiet-105 and Prelu-2.

Mechanism of Action
Bontril PDM / SR acts exerts its effect as an appetite suppressant by targeting the central nervous system, which is comprised of the brain and spinal cord. The active ingredient is actually a prodrug of phendimetrazine meaning that phendimetrazine must be metabolized by the body in order to become active.

Dosage and Administration 
Bontril is available in tablets and capsules. The standard immediate-release form is labeled as PDM, a reference to the active ingredient phendimetrazine. It is a 35mg tablet most often prescribed for use two to three times per day, to be taken orally 30-60 minutes before each meal. The sustained-release formula is taken as a single dose of one 105mg tablet taken 30-60 minutes before the morning meal each day. 105 mg and 35 mg are the most popular doses of Bontril.

Due to its effects on the heart and circulatory system, Bontril PDM / SR is not recommended for use in anyone with a history of high blood pressure, glaucoma or heart disease. It is also contraindicated in anyone with a history of thyroid problems. Its activity in the central nervous system makes Bontril PDM / SR contraindicated for anyone with a history of mood disorders. Due to its potentially habit forming nature, Bontril PDM / SR is not to be prescribed to anyone with a past history of drug addiction or abuse.

Bontril PDM / SR is known to interact with 440 different drugs including some medications used to treat diabetes and high blood pressure. It is not recommended for use in anyone who is also taking some types of antidepressants, cold medications, some antibiotics, other weight loss medications or chemotherapy drugs. Bontril PDM / SR has been shown to cause birth defects and should never be used by women who are pregnant.

History
Phendimetrazine was discovered in Germany in the 1950s. Bontril was FDA approved for use as an appetite suppressant in the 1960s. With the expiration of the original patent, many generic forms became available. Since then, phendimetrazine has become one of the most commonly used prescription diet aides in the country.

Adverse Effects
Bontril PDM / SR can lead to a serious allergic reaction in some people, signs of which can include hives, breathing problems, and/or swelling around the face or in the throat. Other serious side effects associated with Bontril PDM / SR can be related to its effects on the heart. This can lead to a sensation of shortness of breath, chest pain, palpitations and swelling of the feet or ankles. Extremely high blood pressure can cause what’s known as a hypertensive crisis, another possible and dangerous side effect from using Bontril PDM / SR. The symptoms associated with this medical emergency can include severe headache, confusion, blurred vision, ringing in the ears, chest pain, heartbeat irregularities, shortness of breath and even seizure. Bontril PDM / SR may also cause life-altering confusion, irritability, extreme mood swings, unusual thoughts and erratic behavior.

There are also several side effects associated with the use of Bontril PDM / SR that are not considered medical emergencies or cause to discontinue the medication. Many sufferers, however, find these effects disturbing nonetheless. These less serious effects are related to the stimulatory nature of Bontril PDM / SR and can include sleep disturbances, restlessness, hyperactivity, dizziness, tremors and changes in sex drive. Other important side effects include headache, flushing spells similar to hot flashes, dry mouth and digestive upset including constipation, diarrhea and upset stomach.

Any or all side effects may occur even at prescribed doses and are more likely to occur if Bontril PDM / SR is misused or abused.

 

Why does Belviq have serious side effects?

For the first time in 13 years, the Federal Drug Administration has approved a prescription medication and diet pills that claims to help obese patients lose weight in combination with diet and exercise. The increasing rate of obesity in the United States is a possible cause for the authorization, but use of the drug carries significant risks.

General Information
Intended as part of a weight management program that includes reduced caloric intake and exercise, Belviq is not available for everyone. Doctors prescribe the drug only for clinically obese adults whose body mass index (BMI) is 30 or more and for other adults whose BMI is 27 or more. To quality for use of the drug, patients also need to show the presence of at least one weight related problem such as high blood pressure, joint pain, type 2 diabetes, hormonal imbalance, high cholesterol, difficulty sleeping, gerd, stress incontinence or others.

Ingredients
The main ingredient in Belviq is lorcaserin hydrochloride. The drug, formulated by Arena Pharmaceuticals, also contains hydroxypropyl cellulose NF, silicified microcrystalline cellulose, roscarmellose sodium NF, and hydroxypropyl cellulose NF.

Brand Name Variations
The scientific name for the brand Belviq is lorcaserin, and other brand names are not currently in use.

Mechanism of Action
Belviq is supposed to act on receptors that activate the production of proopiomelanocortin and create a feeling of satiety. Scientists think that the affected receptors aid in regulating appetite, but the precise mechanism that performs the process is not known.

Dosing and Administration
Belviq is a 10 mg tablet that patients take orally twice a day. Patients who fail to achieve a weight loss of five percent after 12 weeks of use are not eligible to continue taking the drug. Physical and psychological dependence can result from taking more than the recommended dosage.

History
In December of 2009, Arena Pharmaceuticals submitted an application to the FDA, and it was accepted in February of the following year. In September, the FDA scheduled an advisory committee meeting and issued a letter the following month stating concerns about the new drug. More than a year later, Arena Pharmaceuticals submitted its response to the objections expressed by the FDA. In May of 2012, the advisory committee agreed that the benefits of the drug outweighed its risks, and approval was granted in June of 2012. Preliminary testing of the drug showed that a control group of patients who used it lost about three percent more weight than those who were given a placebo.

Adverse Effects
Some of the common adverse effects of taking Belvig as prescribed include these:

• constipation
• dizziness
• nausea
• headache
• dry mouth
• tiredness

However, many other adverse effects are much more serious. Doctors need to know immediately if symptoms like these occur:

• thoughts of suicide
• depression
• irregular, slower than normal or faster than normal heartbeat
• mood changes
• enlarged breasts
• abnormal production of breast milk
• confusion
• memory problems
• difficulty in maintaining normal attention level
• shortness of breath
• increased incidence of bruising or bleeding
• swelling in hands, feet or ankles

In addition, the drug may cause serotonin syndrome in patients who take other drugs that increase the production of serotonin. The condition is serious and needs immediate medical attention if symptoms like these occur:

• hallucinations
• rapid heartbeat
• severe dizziness
• unexplained fever
• restlessness
• severe vomiting, nausea or diarrhea
• twitching muscles

Patients who take medication for diabetes can experience adverse effects from the drug that increase the risk of having low blood sugar. Males may experience a prolonged and painful erection that can last for four or more hours, and immediate medical attention is required to avoid permanent problems.

Pregnant women are strongly advised to avoid taking Belviq as it may cause harm to a fetus. Weight loss during pregnancy may also cause harm to an unborn baby. The FDA recommends that nursing mothers discontinue taking the drug or stop nursing.

 

The Facts About Taking Meridia/Reductil/Sibutramine

There are many prescription weight loss medications available that can help obese individuals lose weight. These pills typically do not require the patient to start a rigorous exercise program or convert to a difficult diet plan in order to be effective. While prescription diet pills have proven to be successful with helping individuals lose weight, they are also associated with a wide assortment of health risks. Meridia has been linked to causing strokes, increased heart rate, and various other cardiovascular issues. Here are the facts about Meridia and why it was considered to be too harmful to remain on the market as an effective prescription weight loss option.

General Information

Meridia was a once a day weight loss pill that was only available by prescription. It was pulled from the market by the Food and Drug administration in 2010 because it was shown that the drug raised the risk of heart attack and stroke. Along with the serious health risks involved, Meridia also seemed to offer less than stellar benefits to those who took it. At the time when the FDA pulled the drug from the market, there was an estimated 100,000 individuals taking the drug in the United States.

Ingredients

Meridia contains the active ingredient Sibutramine. This oral anorexiant is usually available in the form of hydrochloride monohydrate salt. Up until the year 2010, the drug was prescribed to treat exogenous obesity. It has since been pulled from the market due to its association with strokes, heart attacks and other cardiovascular conditions.

Sibutramine is a serotonin norepinephrine reuptake inhibitor. This combination caused it to have severe interactions with MAOIs and drugs that inhibit CYP3A4 such as erythromycin or ketoconazole. When taken with MAOIs, Sibutramine could increase the patient’s risk of serotonin syndrome.

Brand Name Variations

Meridia is the brand name for the drug Sibutramine. This active ingredient was manufactured and sold under a wide variety of names, including Reductil and Sibutrex. All drugs that contained sibutramine were discontinued at the same time in 2010 by the FDA.

Mechanism of Action

Meridia provides a therapeutic effect through the inhibition of the ingredients serotonin, norepinephrine and dopamine reuptake at neuronal synapses. By stopping the reuptake of these neurotransmitters, Meridia can provide the user with a decrease in appetite. This helps the patient to lose weight because they are consuming less food. Studies have shown that the active ingredient sibutramine may also promote energy through thermogenic effects.

Dosage and Administration

While it was still being prescribed by physicians, the recommended starting dosage of Meridia was 10 mg, once per day, with or without food. The dose could be increased over time if the results were not satisfactory. After four weeks, physicians could increase the dosage to 15mg once per day. It was not recommended that any patient be prescribed a dosage of Meridia above 15 mg per day. Most individuals would take Meridia in the morning, and it could be taken with or without food.

History

Sibutramine was first discovered as a drug in 1987. At the time, the neurotransmitter was investigated to be used as an antidepressant. That is because it behaved similar to other serotonin and norepinephrine uptake inhibitors. The ability to reduce the uptake of serotonin made experts particularly interested in the drug and its possibilities.

As it was being studied as a new antidepressant, many experts took note of the effect that sibutramine had on obese patients. It seemed that the drug was causing a very noticeable decrease in weight. This discovery led to sibutramine being used as an anorexiant drug. It was approved by the FDA in 1997 to treat clinically obese individuals and marketed by Knoll Pharmaceuticals. The ingredient was added to brand name weight loss drugs Meridia and Reductil.

In 2010, Sibutramine was pulled from the market due to its association with being linked to several cardiovascular disorders and strokes. It is no longer available to be prescribed as a weight loss pill.

Adverse Effects

Some of the least common side effects that were associated with Meridia and Reductil include achiness, chills, irregular heartbeat, high blood pressure, depression, swelling of the feet and ankles. The most common adverse effects include anxiety, constipation, headache, trouble sleeping, nervousness, dizziness and irritability.

The most severe effects that patients received after taking a product containing sibutramine were cardiovascular issues such as a fast heartbeat or heart attack, and stroke. The drug was also known to have very harmful interactions with other drugs containing Serotonin.

 

Xenical – Weigh the Benefits and the Risks

General Information

Many people who are overweight look for that elusive miracle that can help them shed pounds. Sometimes the hopeful weight loss aid is a type for food; however, most often people looking for quick relief in the form of pills. Xenical is one of those weight loss medications that is taken in capsule form. The active ingredient in Xenical is Orlistat.

Ingredients

Xenical capsules also contain the following inactive ingredients: cellulose, microcrystalline, Sodium Starch Slycolate Type A Potato, sodium lauryl sulfate povidones talc, gelatin titanium dioxide, FD&C Blue No.1, and shellac

Brand Name Variations

The nonprescription version medication is known as Alli.

Mechanism of Action

Orlistat, whether taken in its prescription form Xenical or it the over-the-counter option, Alli, is used with a low calorie diet, physical activity and behavior modification to help overweight individuals lose weight. In order for the fat to be absorbed in the intestines, it needs to be broken down into small pieces during digestion. Xenical and Alli work by blocking the enzyme that breaks down fat, meaning that if the fat is not broken down, it is not absorbed and passes through the body. One interesting observation is that if a user of Orlistat in either form consumes other foods that are high in calories, he or she may continue to gain weight or maintain the same weight. No matter which form is used, an individual should consume no more than thirty percent of calories from fat. When consuming fat, the amount of fat in meals and snacks should be spread out through out the day.

Dosing and Administration

The prescription dose of Xenical (Orlistat) is 120 mg The recommended non-prescription dose is 60 mg. The medication is in capsule form and self-administered and can be taken during meals and can be taken up to one hour after meals.

History

Xenical (Orlistat) was approved by the FDA in 1999 as a drug to help in weight management. Orlistat the active ingredient in Xenical was approved by the FDA for over-the-counter sales in 2007.

Adverse Effects

In the haste to find a medication that can help with weight loss, it is wise to weigh all of the pros and cons. Just because a medication has been approved by the FDA and has been successful for some does not make it practical or safe for anyone who wants to use it. Before taking Xenical or Alli, there are some risks that should be carefully considered.

Those taking Xenical or Alli should be aware that it can cause a deficiency in vitamins A, D, E, And K. These vitamins are fat soluble, so adequate fat absorption is necessary for them to be absorbed. For this reason, Xenical and Alli users may need to take multivitamin supplements.

Xenical and Alli can also work against anti-rejection or immunosuppressants taken by transplant recipients, and drugs used to treat overactive thyroid conditions. Both medications can also interact with blood thinners. Additionally, there have been some cases of Xenical causing liver damage.

One of the very unpleasant side effects of Xenical is digestive discomfort. The medication can cause stomach cramps and excess flatulence. When excess fat is eaten while taking the medication, there can be a problem with getting to a bathroom in time. Some people experience an urgent need to have a bowel movement, which can result in flatulence that leaves a stain in the underwear. This can be embarrassing when it occurs during the workday or when one is attending a special event.

 

Understanding Prescription Versus OTC Diet Pills

The purpose of diet pills is to help you lose weight. This is achieved by using appetite suppressants that suppress your appetite and ingredients that speed up your metabolism and burn more calories. Usually, OTC diet pills are not as safe as prescription diet pills since they are not FDA monitored. However, there are many people hoping to lose weight who turn towards OTC diet pills because they can either not get prescription for diet pills or can simply not afford them.

Before taking any weight loss formula like diet pills or supplements, it is important to go through their ingredient list, information, product description, possible side effects and history so that there are no surprises. The following are a few differences between prescription and OTC diet pills –

• General Information – It is fairly easy to purchase OTC diet pills as they can be bought from health food stores, grocery stores and online shops. There are no prescriptions necessary for OTC diet pills but it is advisable to consult your doctor before you decide to take one. With prescription diet pills, however, a doctor needs to be seen first. After evaluating your BMI and overall health, the doctor would be able to prescribe a diet pill. Usually, diet pills are prescribed for BMI that is greater than 30 or, for people suffering from diabetes and hypertension, over 27.

• Mechanism of Action – OTC diet pills come with various herbs that combine to suppress the appetite and increase burning of calories in your body. Thus, the metabolism works at a faster rate and the fat that is absorbed by the body is reduced. With prescription diet pills, the aim is to reduce almost 10% of body fat so that diseases related to lipid levels, blood sugar levels, and blood pressure can be prevented.

• Side Effects – OTC diet pills are not monitored by the FDA and thus, you can never know if they are safe enough for consumption. The ingredients that are used in OTC pills also lack sufficient evidence to prove their safety or effectiveness. The best example for this is the ingredient Ephedra which has such severe cardiovascular risks that its US sale was banned by FDA. Another ingredient is bitter orange which is deemed unsafe but successfully burns calories. Usually, OTC diet pills come with side effects like anxiety, nausea, dizziness, hypertension, seizures, liver damage, diarrhea, increased urination, kidney damage, strokes and heart attack.

Prescription pills, however, are monitored by FDA to ensure their safety and efficiency. But this doesn’t mean that prescription pills come without any side effects. Common side effects associated with prescription pills are dizziness, hypertension, increased heart rate and effects on the gastrointestinal system.

• Price – Prescription diet pills are usually costlier than OTC diet pills, which is one of the main reasons why people lean towards OTC diet pills.

• Are natural supplements as effective as other diet pills? – It’s a fact that most diet pills are riddled with side effects and more problems but that does not mean that all of them are the same. There are diet pills in the market which are relatively safe and their benefits outweigh their negatives. In the same way, not all natural supplements are effective as diet pills but there is a few which seem to hit the mark. In fact, most of the ingredients in natural supplements like HCA, Chitosan, Whey protein, Beta Glucan, CLA, Glucomannan and mango seed fiber, are used in many diet pills to enhance the properties of other ingredients.

• Are diet pills or over-the-counter diet pills more effective? – As mentioned before, there are pills in both prescriptive and OTC categories that fail and have side effects, and there are pills in both the categories that perform wonders. But overall, if the safety of the pills is taken into account, OTC diet pills seem to have more side effects. This is mostly due to the fact that there is no substantial research that supports the claims made by OTC diet pills.

The OTC diet pills that work well are those that come with all the supported research and proof of their effectiveness.

In conclusion, it is important to buy those pills which should scientific proof of their working and results, instead of relying on media hype and fraudulent claims.

 

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