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Advair 250

Advair 250

A brief guide to Advair 250 50

Advair Diskus is prescribed to patients who have severe asthma symptoms that cannot be relieved by long-term medications. The Advair 250 dosage will be prescribed to patients differently depending on ailment: patients with chronic obstructive pulmonary disorders (COPD) such as bronchitis will only take the drug in the Advair 250 mg (micrograms) dosage; Asthma patients will be assigned Advair 250 for short-term use to control symptoms; COPD sufferers may be prescribed Advair Diskus 250 50 for long-term use.

When a physician assigns Advair Diskus 250 50, they will explain that the former number refers to the micrograms of the active drug, while the latter refers to the inhalation powder. Before assigning Advair 250 mg, a doctor should make sure that you do not have any allergies to dairy products, particularly milk. Said allergies will inform your doctor that your body cannot adequately absorb or digest Advair 250 50.

If you are an asthma patient, you will not be assigned Advair Diskus 250 50 at the beginning of your treatment plan. Instead, you will begin with a smaller 100 microgram dosage. After observing how your body responds, your physician may increase your dosage to Advair 250 mg if relief from serious symptoms is not obtained. Should positive results still not be observed, a physician may increase your dosage from Advair 250 to the 500 mg dose.

Because the drug has been known to increase the risk of asthma-related deaths with prolonged use, asthma patients will be assigned Advair Diskus 250 50 on a short-term basis. Once severe symptoms have abated, physicians will decrease your dosage from Advair 250 mg to a lower dosage, with the goal of ending intake altogether. COPD sufferers may be assigned Advair 250 on an indefinite, long-term basis.

In either circumstance, it is important to be alert to any sign of adverse reaction while taking Advair Diskus 250 50. Some negative responses to intake of Advair 250 mg, such as headache or nausea, are not unique to the drug. Allergic skin reactions such as developing a rash or hives are serious and may indicate that should discontinue using Advair 250. All negative side effects associated with Advair use should be reported to your physician immediately. Advair 250 mg use in asthma patients is not intended as a substitute for emergency inhalers.

The Advair 250 medication requires 2 applications per day; allow twelve hours to pass between each dosage of Advair Diskus 250 50. Never exceed—in dosage strengths or frequency–a physician's guidelines concerning Advair 250 mg use.

 

Pergolide-Permax

Pergolide-Permax

 
What is Pergolide?
 
 
Also referred to as Permax, Pergolide is an ergoline-based dopamine receptor used in some countries for the treatment of Parkinson’s disease. 
Parkinson’s is associated with abnormally low levels of the neurotransmitter dopamine in the brain Pergolide (commercial name Permax) attempts to mimic—and yield similar effects–as dopamine in the body.
 
 
Although effective in numerous case studies, Pergolide was withdrawn from the United States consumer markets for human use. The ban came after several published studies revealed a link between Pergolide and increased rates of valvular dysfunction. Although banned for human use, Pergolide is applied for use in animals, particularly horses, to treat Cushing’s syndrome.
Pergolide (Permax) is provided via oral administration in tablets. With Pergolide acting as the base, the tablets utilize microcrystalline cellulose, magnesium stearate, lactose monohydrate, sodium starch glycolate and pregelatinized starch. 
 
 
As a dopamine receptor agonist, Pergolide (Permax) is 10 to 1000 times stronger than bromocriptine on a milligram per milligram basis. Pergolide (Permax) impedes the secretion of prolactin in human beings; Pergolide (Permax) causes a transient increase in serum concentrations of growth hormones and a steady decrease in serum concentrations of luteinizing hormones. To combat Parkinson’s disease, Pergolide (Permax) is thought to exert a therapeutic effect by stimulating post-synaptic dopamine receptors in the body’s nigrostriatal system. 
 
 
Is Pergolide Banned Throughout the World?
 
 
Pergolide (Permax) is not available in the United States; however, it is still commonly used in a handful of countries for the treatment of various conditions, including restless leg syndrome, hyperprolactinemia and Parkinson’s disease. Moreover, Pergolide (Permax) is also used for veterinary purposes—the drug is commonly used to treat pituitary par intermedia hyperplasia or—as stated above—Equine Cushing’s Syndrome in horses. 
 
 
Side Effects of Pergolide:
 
 
Pergolide, which has significantly decreased with regards to circulation and use, is commonly associated with a form of heart disease called cardiac fibrosis. In 2007, the Food and Drug Administration declared a voluntary withdrawal of Pergolide (Permax) by manufacturers because of the increased possibility of heart valve damage. As stated above, Pergolide (Permax) is not available in the United States. 
 
 
The dangerous side effects yielded by Pergolide (Permax) are thought to be caused by the drug’s action at the 5-HT serotonin receptor of cardiac myocytes; this effect causes proliferative valve disease in a similar manner to other serotonin agonists. Pergolide (Permax) can also cause Raynaud’s phenomenon and impair associative learning. 
 
 
Patients using Pergolide (Permax) commonly report falling asleep while engaged in daily activities, including driving a car. Although a number of patients reported somnolence while taking Pergolide (Permax), a large percentage reported a lack of warning signs such as drowsiness before falling asleep. 
 
 
In Clinical trials, roughly 10% of patients taking Pergolide (Permax) exhibited signs of symptomatic hypotension, especially during the initial phases of treatment. With gradual increase of Pergolide (Permax), patients grew tolerant of the hypotension. It is therefore necessary to be cognizant of the risk; treatment must begin with low doses and only increase if the patient can tolerate hypotension. Typically, dosage is increased over a period of 3 to 4 weeks. 
 
 
In controlled tests, Pergolide (Permax) caused hallucinations in roughly 15% of patients. The hallucinations were intense enough to cause a discontinuation in roughly 3% of those affected. 
I a placebo-controlled test, 2 of 187 patients treated with Pergolide (Permax) died. Of the 2,3000 patients treated with Pergolide (Permax) in premarketing tests (conducted in the late 1980’s), 143 patients died while under the drug or shortly after taking it. Because the patient population under evaluation was ill, elderly, and/or facing increased risks of death, it was affirmed that Pergolide (Permax) played a minor role in these fatalities. However, the possibility that Pergolide (Permax) shortens survival times cannot be excluded with absolute certainty. 
 
 
In addition to the physical ailments caused by Pergolide (Permax), the drug has reported to cause unique psychological alterations. In Britain, for example, select users of Pergolide (Permax) claim that the drug has caused them to develop severe gambling addictions. In June of 3010, similar reports surfaced in Australia; users of Pergolide (Permax) are suing the manufacturer over both gambling and sex addiction problems they claim resulted from the use of the drug. 
 
 
In March of 2007, manufacturers of Pergolide (Permax) agreed to withdraw the medication from the United States after a number of published studies revealed a link between the drug and heightened rates of valvular dysfunction. 
 
 
In addition to the aforementioned side effects, Pergolide (Permax) causes a significant decrease in appetite during the first week of use. Other side effects commonly associated with Pergolide (Permax) include: anemia, respiratory infections, hallucinations, dizziness, headache and low blood-pressure. 
 
 
Pergolide (Permax) Recall and Legal Information:
 
 
A gradual recall of Pergolide (Permax) was announced on March 30th of 2007. The recall was announced by officials within the United States Food and Drug Administration and came after a decade of progressively increased warnings by both the Food and Drug Administration and the drug’s parent company, Eli Lilly. 
 
 
If you or a loved one has suffered a serious injury or death as a result of Pergolide (Permax), you must immediately contact a law firm that specializes in mass torts, drug side effect lawsuits or personal injury laws. These types of law firms will handle Pergolide (Permax) associated legislation in all 50 states throughout the U.S. 
 
 
Those victims filing lawsuits against manufacturers of Pergolide (Permax) commonly seek compensation for the following side effects:
 
 
1. Primary Pulmonary Hypertension
 
 
2. Heart-Valve Damage (Mitral and Aortic Valve injuries)
 
 
3. Valvular heart diseases
 
 
4. Cardiac valvulopathy
 
 
5. Leaky heart valves
 
 
6. Pulmonary fibrosis (pleural, pericardial and/or retroperitoneal fibrosis)
 
 

Advair Diskus 250 50

Advair Diskus 250 50


A brief guide to Advair Diskus 250 50

The medication Advair Diskus 250 50 represents the medium dose of Advair—the popular asthma and respiratory medication. Advair Diskus 250 for relief of symptoms related to severe respiratory problems, such as bronchitis can be continued on a long-term basis. However, asthma patients prescribed Advair Diskus 250 50 face increased risks if used long-term. Therefore, when combatting asthma, the Advair Diskus 250 50 must be regularly monitored.

Prior to issuing a prescription for Advair Diskus 250, a physician must question you about your medical history, including any medications you are currently taking. Advair Diskus 250 50 should not be issued patients who are allergic to milk. Additionally, conditions such as epilepsy or thyroid problems are among those which could place you at an increased risk of adverse effects when taking Advair Diskus 250. After evaluating your medical history, a physician will determine whether Advair Diskus 250 50 is likely to be safe and efficacious.

Your doctor is responsible for explaining all the potential adverse effects that may ensue as the result of Advair Diskus 250 use. The bulk of effects, such as headaches or stomach problems, are common to many prescription medications. Because treatment with this drug can weaken your immune system, patients on Advair Diskus 250 face an increased risk of pneumonia and other illnesses. Report all observed side effects, no matter how minor, to a physician as soon as possible. If you develop a rash, hives or similar skin problems, your body is experiencing an allergic reaction to Advair Diskus 250 50.

Advair Diskus 250 50 should be taken twice a day via the inhaler. Doses should be administered every 12 hours. Advair Diskus 250 is not intended to provide immediate relief for breathing problems, nor is it a substitute for emergency inhalers. Under no circumstances should you take more than two doses of Advair Diskus 250 50 a day. If you forget to take the drug, do not take two doses of Advair Diskus 250 at the same time to catch up.

Serious side effects which occur as the result of overuse of the drug are your sole responsibility. However, if you follow a doctor's directions for use of Advair Diskus 250 50 but still experience medical problems; you may have grounds for a lawsuit. A physician who has not properly monitored your body's response to the medication may be guilty of malpractice. Consult with a lawyer who specializes in such cases to see if a clear link between their actions and serious health effects can be established to the satisfaction of the law.

 

Prempro

Prempro

What is Prempro?
 
 
Prempro is a dangerous drug that contains medroxyprogesterone and a combination of conjugated estrogens (a mixture of estrogen hormones). Estrogen is a female sex hormone created by the ovaries that is essential for a number of bodily functions. Medroxyprogesterone—typically called “progesterone”– is another female hormone crucial for the regulation of menstruation and ovulation. 
Prempro is widely used to treat the symptoms associated with menopause, including vaginal dryness, hot flashes and irritation. Moreover, Prempro is used to prevent osteoporosis (thinning of the bones). 
 
 
Prempro should not be administered to prevent dementia or heart disease; the drug should not be taken as a treatment for these conditions because it will adversely increase the patient’s probability of developing said conditions. 
 
 
Prempro: What you must know
 
 
It is crucial that you do not take Prempro if you have any of the following conditions: stroke, history of heart problems, liver disease, blood clots (particularly in your lower body or lungs), abnormal vaginal bleeding or hormone-related cancer, such as uterine or breast cancers. Prempro may also adversely affect unborn babies or increase the probability of infant fatalities; do not use Prempro if you are pregnant. 
 
 
Long-term use of Prempro may significantly increase your risk of heart attack, stroke or breast cancer. If you are using Prempro, you must consult with a doctor regarding the individual risks. Consultations with a medical professional are necessary if you are overweight or smoke while using Prempro. Your doctor should check your progress every 3 to 6 months to determine whether you should continue Prempro treatment. To ensure proper administration, you should have regular physical exams; you should also perform self-examinations on your breasts (check for lumps) at least once a month. 
 
 
Again, Prempro should never be used to treat dementia or heart disease, because the medication may actually increase your risk of developing said conditions. 
 
 
What to do before taking Prempro:
 
 
Remember, you should not use Prempro if you experience any of the following conditions:
 
 
Liver disease
 
 
Abnormal vaginal bleeding that has not been checked by a medical professional
 
 
History of heart attacks, strokes or blood clots—particularly those in your lower body or lungs
 
 
Any form of uterine, hormone-dependent or breast cancer
 
 
If you have developed any of these conditions, you should undergo special tests to ensure that you can safely ingest Prempro. Moreover, if you have any of the below conditions, you must seek professional help to gauge your ability to handle Prempro:
 
 
Heart disease, high blood pressure or circulation difficulties
 
 
Endometriosis
 
 
Kidney or liver disease
 
 
Asthma
 
 
Seizure disorders (epilepsy)
 
 
Diabetes
 
 
High Cholesterol (triglycerdies)
 
 
High or low levels of calcium in the blood
 
 
System Lupus Erythematosus
 
 
Gallbadder ailments and/or diseases
 
 
If you have ever had your uterus removed (hysterectomy)
 
 
Conjugated estrogens may increase your risk of developing endometrial hyperplasia—a medical condition that increases the risk of developing cancer in the uterus. Ingesting progestins while taking conjugated estrogens may decrease this risk. If you have not undergone a hysterectomy, your doctor may opt to prescribe a progestin for you to take while on Prempro. 
 
 
Long-term conjugated estrogen medications may increase your risk of developing blood clots or strokes. It is important to talk with your doctor concerning your individual risks before undertaking long-term conjugated estrogen treatment. This need intensifies if you are overweight or are a smoker. Again, your medical professional must check your progress on a regular basis (typically every 3 to 6 months) to determine whether you should halt or continue treatment with Prempro. 
 
 
In addition to the aforementioned side effects, Prempro may also cause significant birth defects. Because of this, it is essential that you do not take Prempro if you are pregnant. Before prescribing or suggesting Prempro, you must immediately notify your doctor that you are pregnant. If you are already on Prempro and become pregnant you must tell your doctor right away. To avoid this scenario, you should use an effective form of birth control (or a combination of birth controls) while using Prempro. 
 
 
Birth defects caused by Prempro occur because conjugated estrogens and medroxyprogesterone pass into breast milk and disrupt nursing babies. Prempro may also impede your ability to produce breast milk. Because of these side effects, it is a necessity that you do not use Prempro if you are breast-feeding a child. Also, it is strongly suggested that you do not give Prempro to any individual under the age of 18 years old without first consulting with a medical professional.
 
 
How do I take Prempro?
 
 
You must take Prempro exactly as it was prescribed by your doctor. It is strongly suggested that you do not take Prempro in larger or smaller amounts or use it longer than as it is recommended by your doctor. It is necessary to follow the directions on your prescription label. 
 
 
You may consume Prempro with or without food. You should try and take the medication at the same time each day. It is suggested that you take Prempro regularly to achieve the best results. If you miss a dose, skip it, and take your Prempro at the next regularly scheduled time. Never take an extra dose if you missed a cycle of Prempro. 
It is also important to avoid smoking when using Prempro. Smoking will increase your risk of developing blood clots, strokes or heart attacks. If you overdose on Prempro you must seek emergency medical attention or contact the Poison Help line at 1-800-222-1222. 
 
 
 
 

Fast Facts about Ketamine

Fast Facts about Ketamine

What Is Ketamine
Ketamine is a drug that has dissociative anesthetic properties. It is most often found as a white to slightly off-white powder or an odorless, colorless liquid. It is a very quick acting substance with a very similar structure and action as PCP, although it is slightly less potent than PCP pas an anesthetic.
Street names for ketamine include K, Special K, jet, Green, Super Acid, Honey Oil, Ket, and Special la coke.
Effects of Ketamine
While it has legitimate uses for both animal and humans, it is also known to be abused because of its hallucinogenic properties. However, at higher does it is no longer used just as an anesthetic but can cause more severe effects such as changes in body image and mood as well as hallucinations.
Immediate effects of ketamine include sensory distortion, out of body experiences, lack of sense of time, aggressive behavior memory problems, and numbness.
Ketamine use has also been correlated to many mental and physical problems such as depression, amnesia, delirium, impaired motor function, hypertension, and respiratory problems.
Ketamine Abuse
As a “club drug,” ketamine is often abused by teens and young adults in order to distort sensory perception and create a sense of disconnect from the body. While other club drugs such as PCP or LSD have much longer effects, the effects of ketamine typically lasts between 30 to 90 minutes.
Because of its properties as an anesthetic, ketamine is often used by sexual predators to as a date rape drug to incapacitate a potential victim. Often victims are aware of the actions around them, but are not able to move or respond accordingly.
Teens and young adults ages 12 to 25 were responsible for 74% of ketamine abuse that resulted in involvement of an emergency department. Approximately 3% of high school students have tried Ketamine at last once. 

Ketamine and the Law
Ketamine is considered a Schedule III controlled substance according to the Controlled Substance Act. Other Schedule III drugs include anabolic steroids. While Schedule III drugs are not as addictive as other drugs such as heroin or cocaine, Ketamine abuse can still lead to a level of psychological or physical dependence.

Beryllium

Beryllium

Working with Beryllium


Beryllium is a steel-gray brittle metal found in part of oil, coal, volcanic dust, and soil. In the elemental form, it is the second lightest metal and has many different applications. 
The first commercial application of beryllium was in 1918 when a beryllium-aluminum alloy was patented, which started the industry’s use of beryllium. Because of beryllium’s stiffness, light weight, high strength, low density, high melting point, and good electrical and thermal conductive properties, it quickly became used in the industry.
Today, beryllium is often used in the nuclear, aerospace, and manufacturing industry. It is also commonly used in golf clubs, dental appliances, wheel chairs, non-sparking tools, and certain electronic devises.
Despite beryllium being a commonly used metal, it is highly toxic and prolonged exposures above certain threshold values can cause acute or chronic beryllium disease. The toxic effects are most commonly observed through beryllium exposure via an inhalation pathway.
The acute disease begins not long after exposure and can often bronchitis or pneumonia. The acute form requires high levels of exposure to occur and because of protective measures to reduce exposure, it is rare.
The chronic form of the disease takes longer to develop in comparison acute form. Onset can vary and may happen from several months to years after beryllium exposure. The chronic for needs much lower levels of beryllium exposure. Furthermore, scarring and lung inflammation make it difficult oxygen to get into the body via the bloodstream.
Symptoms of chronic beryllium disease are:
Shortness of breath
Chest pain
Cough
Fatigue
Loss of appetite
Weight loss
Once in the body, beryllium can complex with a protein and deposit in the spleen, kidneys, and liver, but when combined with a specific biological protein, can result in the chronic disease resulting in toxicological effects on the lungs and the alveoli within them.
Because of the potential dangers of beryllium, it is very closely regulated in its industry use in order to protect workers who handle the metal directory. Because of this, the metal is relatively safe to work with in many industries.


Safety Policy
In accordance to the Occupational Safety and Health Administration, there are necessary safety precautions to prevent overexposure to beryllium.
Minimize the airborne concentration and reduce the possibility of contamination.
Use a safety mask when working with beryllium and be aware of safety procedure.
Wash hands after contact with the metal.
Cover the localized workspace with paper.
Try to work in a small and centralized area of the paper.
Use tape to trap any beryllium particles, and ensure the dust does not escape.
Wrap up the contaminated paper and dispose of it in a plastic bag that is clearly labeled.
Give the beryllium waste to the Beryllium safety contact person.
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Adipex Coupons

Adipex Coupons


How to find Coupons for Adipex

The prescription medication Adipex is an appetite suppresant that should only be used for a limited period of time. Due to the drug’s relatively short treatment course (Apridex is often prescribed for 12 weeks), you may be able to afford the medication even without an Adipex coupon. That being said, it is always a good idea to research all of your payment options in hopes of reducing your total cost.

Adipex coupons can be obtained from a number of sources. Currently, the official website of the manufacturer has an Adipex coupon which may be printed to help you procure a first batch of 30 pills at a discounted price. Coupons for Adipex may also be found from a number of insurance companies and health providers. To ensure a reduced price, please ask your physician whether they have access to any Apidex coupons.

Regardless of where you procure Apridex coupons, they cannot be used without a physician's prescription. Once it has been obtained, you must find out whether any restrictions are placed upon the use of coupons for Adipex. For example, depending on terms of your insurance coverage, you may not be able to use Adipex coupons for purchase of the drug from an online merchant. Additionally, the Adipex coupon itself may place restrictions upon its use.

Offers of coupons for Adipex purchases are perpetually changing. If your physician is not able to refer you to a source for Adipex coupons, you may choose to conduct research online. However, you should be careful when searching for Adipex coupons, because similar to other financial offers, coupons for Adipex purchases may be fraudulent or attached with dangerous fine print. Be sure to research the provider of any Adipex coupon before activating it.

If you decide to purchase the drug online, you should be able to find a pharmacy which is willing to accept the Adipex coupon. Make sure that you do not use an Adipex coupon to purchase the drug from any pharmacy which does not require a prescription. Such businesses are not to be trusted to provide the correct medication, since they are engaging in illicit transactions. Similarly, do not use coupons for Adipex to purchase these drug foreign pharmacies. Despite the discount offered by an Adipex coupon, foreign pharmacies are not regulated by American law.

Regardless of whether you use Adipex coupons or not, you should be able to purchase medication and trust that it will not harm you. Litigation, if you experience severe adverse effects after using coupons for Adipex, should be initiated to recoup the losses associated with medical expenses, lost wages from missed work and pain and suffering.

If you use Adipex coupons to purchase drugs without a prescription, your litigation efforts will ultimately prove unsuccessful—purchasing Apidex without a prescription is deemed negligent by the courts.

If you fall ill despite following a physician's guidelines, you may have grounds for a lawsuit. Copies of Adipex coupons and a doctor's report will be necessary for a lawyer to pursue litigation.

 

 

Adipex Weight Loss

Adipex Weight Loss

A Brief Guide to Adipex Weight Loss Results

People who are morbidly obese and have trouble losing weight through diet and exercise alone may be prescribed Adipex for weight loss. The efficacy of this drug will vary from person to person. Adipex weight loss cannot be achieved by taking the drug by itself. In order to achieve Adipex weight loss results, a diet and exercise regimen must supplement it.

If you are considering taking Adipex for weight loss, you must consult a physician. It is not legal to attempt Adipex weight loss without a prescription. When meeting with a doctor, the professional must review your medical history before determining whether you are likely to achieve Adipex weight loss results. If a history of addiction or drug abuse is present in your family, a physician is unlikely to prescribe Adipex for weight loss.

When embarking on this course of treatment, your Adipex weight loss treatment will take the form of a 37.5 milligram tablet. The drug should be taken in the morning with or without food.

In some cases, a physician may decide that Adipex weight loss will be better served by ingesting two pills of a half dose. In any case, you should never exceed your prescription guidelines when embarking on a course of Adipex for weight loss. By abusing or exceeding your prescribed dose, the risk of developing an addiction during the course treatment becomes very real.

Apidex treatment should not exceed 12 weeks. Adipex weight loss results are diminishing; the results decrease as your body gets acclimated to the drug. Additionally, it is vital to ensure that Adipex for weight loss does not become habit-forming. Consult with a medical professional if you notice any adverse effects, ranging in severity from insomnia to potentially fatal hypertension in your lungs. It is important to monitor your body’s response and report any irregularities to your medical professional.

It is not possible to predict how much weight you will lose during the course of taking Adipex for weight loss. To ensure maximum efficiency, you must maintain your exercise and diet regimen as prescribed by your doctor. If you do not receive expected Adipex weight loss results, you will not be able to pursue litigation. Prescription medication works successfully for most patients if they stay regimented and dedicated.

If; however, you are medically damaged while taking Adipex for weight loss, it may be possible to pursue litigation. Litigation is initiated to secure a monetary settlement to offset the costs associated with developing the adverse reaction. To file an effective claim you must be able to prove negligence on the part of your doctor or the drug’s manufacturer. Be sure to gather all medical records relating to your Adipex incident/side effect. Lawyers will need to examine these documents to solidify the link between your damage and ingestion of the pill.