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Actonel Class Action Lawsuit

Actonel Class Action Lawsuit


How to join an Actonel class action lawsuit:

The prescription medication Actonel has been associated with several severe side effects. Most notably, patients who have suffered from osteonecrosis of the jaw may be able to join an Actonel class action suit. Actonel class action lawsuits for this particular side effect include hundreds of patients who suffer from “jaw bone death” as a result of Actonel use. So, because you are joining those who share similar stories, you do not have to independently file a claim against Actonel.  

Generally, the defendant in an Actonel class action lawsuit is the manufacturer of the drug, Warner Chilcott Laboratories. Sufferers damaged by the drug's side effects may not always be eligible to join an Actonel class action suit; the individual must endure the same symptoms or be diagnosed with the same medical condition as the other plaintiffs in the Actonel class action suit.

Some of the Actonel’s side effects are common to other medications and will probably not help establish an Actonel class action lawsuit. For example, difficulty sleeping or diarrhea will not provide sufficient grounds to form an Actonel class action suit. Significant, long-lasting medical damage must be the foundation of Actonel class action suits. Since osteonecrosis of the jaw begins with oral pain and can end in the removal of your jaw, it qualifies as grounds for an Actonel class action lawsuit.

If you have been hurt Actonel use, you must immediately consult with your physician to either reverse the reaction or document your condition. In the latter situation, you may be able to join an Actonel class action suit without committing significant resources. Even though these kinds of cases consolidate several plaintiff complaints, only one person is required to represent the group. This person serves as the primary liaison to the defense team.

If you learn that an Actonel class action suit is already being undertaken, you must contact the representing law firm. You should then schedule a meeting to discuss adding your name to the list of plaintiffs in an Actonel class action lawsuit. When meeting with the facilitator, you must present all medical records to document the adverse reacts. This information will serve as the foundation for your Actonel class action suit. The more evidence delivered to the lawyer the more effective the professional will be in proving negligence or fault on the part of the drug maker.  

Depending on the number of plaintiffs involved, resolving an Actonel class action lawsuit can vary in time; some Actonel class actions suits can take years while others will be wrapped up in a couple of short months. Commonly, an Actonel class action suit may be handled by more than one law firm. This is necessary to handle the large volume of documentation involved in an Actonel class action.

You should be kept informed if you request about all progress made in an Actonel class action lawsuit. However, once you have provided your records, you will probably not need to appear in court or directly involved yourself in an Actonel class action suit. You should be notified if and when an Actonel class action results in a financial settlement to be divided among plaintiffs.

 

Zyprexa

Zyprexa

 
Frequently Asked Questions about Zyprexa
 
 
What is Zyprexa?
 
 
Zyprexa is the trade name for the drug olanzapine as manufactured by the pharmaceutical giant Eli Lily and Company. It is termed an atypical antipsychotic and can be used in the treatment of several mental illnesses.
 
 
How is Zyprexa taken?
 
 
There are actually three separate ways that Zyprexa is meant to be taken, but most interestingly, the way that a patient takes Zyprexa determines what its effect will be on them.
 
 
Oral Zyprexa: For the treatment of schizophrenia, both during acute episodes and as a maintenance treatment, as well as for the treatment of bipolar disorder during its manic phases, in which case it used as a supplement to lithium or valproate;
 
 
Intramuscular Zyprexa: Only for acute treatment of schizophrenia of bipolar disorder or manic-phase bipolar disorder, not for maintenance treatment;
 
 
Oral Zyprexa with fluoxetine: For the treatment of the depressive-phase of bipolar disorder, or for adults with depression which is resistant to other medications.
 
 
Some doctors also prescribe Zyprexa to treat anorexia or Tourette syndrome, though those are not FDA approved uses.
 
 
What are the common side effects of Zyprexa?
 
 
Zyprexa can cause several movement disorders, such as Tardive dyskinesia in which involuntary and repetitive body movements occur, and neuroleptic malignant syndrome, which is very rare and potentially fatal, consisting of muscle rigidity, autonomic instability and even cognitive delirium. These movement disorders are common to all drugs in the neuroleptic category.
 
 
More unique to Zyprexa are all of the following side effects:
 
Akathisia or chronic restlessness
 
Anhedonia, or the inability to find pleasure in activities commonly found enjoyable;
 
Auditory Hallucinations;
 
Decreased Motor Skills
 
Dizziness;
 
Dry Mouth;
 
Heart Failure, Heart Attacks, Heart Disease;
 
Impaired Thinking or Judgment;
 
Increased Appetite;
 
Insomnia;
 
Irritability;
 
Menstrual Irregularity;
 
Red Eye;
 
Seizures
 
SSRI Discontinuation Syndrome or Brain Zaps, a risk of withdrawal
 
Trouble Swallowing
 
Vertigo.
 
 
Is there some controversy over Zyprexa?
 
 
Yes, Zyprexa has become a highly controversial medication during the past decade. There are several reasons for this, but one important cause is a side-effect that Eli Lilly & Company is still reluctant to discuss: diabetes. A recent report in The Times of London shows that Eli Lily and company has had information that the use of Zyprexa simultaneously causes weight gain and increased blood sugar levels. Documents going as far back as 1998 show the company worrying about what the weight gain caused by Zyprexa might do to sails. One researcher wrote in a 2000 memo about the drug’s “implications for glucose,” which is a polite way of suspecting it to cause diabetes.
 
 
The actual research conducted by Zyprexa paints a revealing portrait. At least 30% of patients on Zyprexa gained 22 pounds or more because of the drug, and a later study showed that 60% of patients gained at least 66 pounds after just one year on the drug. 
 
 
Two lawsuits resulted from Zyprexa and its ties to weight gain and diabetes. The first, settled in 2006, paid out $700 million dollars to individuals who’d developed diabetes and other diseases while taking Zyprexa. The second which concerned 18,000 other, similar allegations, was worth another $500 million. This means that Eli Lilly has paid out more than $1.2 billion dollars to more than 28,000 patients who’ve suffered from the use of Zyprexa, a huge number until you realize that more than 20 million individuals have taken Zyprexa across the globe, and Eli Lily & Company routinely earns more than a billion dollars from sales of the drug each quarter.
 
 
The other controversy regarding Zyprexa does not directly concern its risk factors for diabetes but rather its prescribed uses, although the seriousness of its side effects is an important factor. After the first phase of Zyprexa’s introduction to the marketplace, when it was a huge success among sufferers of schizophrenia and bipolar disorder, Eli Lilly & Company was pushing for new uses for the drug, even though these uses hadn’t been approved by the Food & Drug Administration.
 
 
Most troublingly, Eli Lilly & Company marketed the drug through its thousands of sales representatives to treat children in foster care, insomniacs, and the elderly in nursing homes. According to Laurie Magid, a U.S. Attorney, the Company’s sales representatives were trained to court nursing home and foster home managers with the slogan “five at five,” meaning that a low dosage of Zyprexa would keep individuals quiet throughout the evening and night. 
 
 
The serious side-effects of Zyprexa made these actions genuinely harmful. Prescribing a individuals with no serious symptoms a drug like Zyprexa, which causes diabetes, huge weight gains, seizures, and the potentially fatal neuroleptic malignant syndrome, as a mere matter of routine, is a hugely negligent act, according to the U.S. Attorney’s Office and Laurie Magid.
 
 
For these crimes, Eli Lilly & Company agreed to pay out $1.4 billion dollars to sufferers from Zyprexa. This means that the total costs of Zyprexa to the pharmaceutical giant now total $2.6 billion.
 
 
What do I do if I’ve been injured by Zyprexa?
 
 
If you’ve been injured by Zyprexa, then you should contact an attorney right away. If your claims appear to fall under the jurisdiction of one of the lawsuits that have already occurred, then you might be entitled to a portion of the billions that have already been awarded. Finding an attorney will help to legitimize your claims and get you your compensation as soon as possible.
 
 
You may also need to file a new lawsuit against Eli Lilly & Company over Zyprexa. Thousands of cases have been tried continuously during the period that these large class-action suits were occurring, and yours might very well be another one, but you should have the input of a noted medical malpractice attorney first.
 
 
Remember that no matter what your claims regarding Zyprexa are, if a medical malpractice attorney agrees to take it, they should charge you on a contingency plan, asking for no money upfront and instead a portion of a trial award or a cash settlement. This also means that they won’t charge you any money if you lose your case.
 
 

Advair Diskus Cost

Advair Diskus Cost

A brief guide to Advair Diskus costs

When you are prescribed the medication Advair Diskus to help control asthma symptoms, you may be concerned with the cost of the medication. The total Advair Diskus cost can be predicted in advance based on its short-term use. Physicians, generally, provide the best estimates concerning the length of your Advair prescription.

Advair Diskus costs may be mitigated by insurance co-pays. You will need to consult your insurance policy carefully to see if the Advair Diskus cost is covered under the terms of your agreement. A policy may only cover Advair Diskus costs up to a certain point, beyond which you may have to pay for the medication yourself.

To secure the lowest possible Advair Diskus cost, you should ask several pharmacies to provide you with a quote. Ask your physician if they know of any local pharmacies which offer the lowest Advair Diskus costs. The manufacturer currently offers a coupon for $10 off of the purchase of a month's supply, as well as a trial offer for a free 30-day-dose for first-time users. Such offers to help control Advair Diskus cost are always subject to change.

Some patients are not close to a pharmacy or may not be satisfied with the quoted Advair Diskus costs. If so, they may choose to see if they can obtain the medication for cheaper online. Should you find pharmacies online whose listed Advair Diskus costs are closer to your budgetary range, you must make sure that they are a legitimate business to ensure you are not taken advantage of. Confirm that any such pharmacy has a pharmacist on staff that can answer questions and requires a prescription before making a purchase.

No matter how low their listed Advair Diskus cost, do not buy the drug from any online pharmacy which is located overseas. Such businesses are not subject to United States regulations and cannot be trusted to provide you with the medication you have paid for. Though you think you may be saving on Advair Diskus costs, you are at risk of having your credit card information misused by such businesses. If so, you will have little legal recourse to recover the Advair Diskus cost you have paid for.

Whatever the listed Advair Diskus costs, you should expect that your usage of the drug is safe. The listed price should not affect the quality of the drug. If you find that serious side effects which you have not been cautioned about ensue, you may have grounds for a lawsuit. Maintain receipts listing what you paid in Advair Diskus cost.

If you have strong grounds for litigation against a physician who failed to properly guide the drug's use or the manufacturer, do not attempt self-representation. If you have a strong case, it will not be hard to find a lawyer willing to help you recover damages and the Advair Diskus cost in return for a percentage of your settlement rather than for a direct fee.

 

New Studies for Stronger Pneumonia Vaccine

New Studies for Stronger Pneumonia Vaccine


On October 15, 2012, the National Institutes of Health (NIH) announced funding that will help researchers find out if a higher dose of a vaccine for pneumonia can create a stronger immunity for older adults who received similar vaccines in the past.  


According to the NIH, the new study will compare results from vaccines given to children between 6 weeks and 5 years old and adults 50 years of age or older.  About 882 men and women between 55 and 74 have elected for the study.


The study addresses one of the largest health epidemics in the United States.  According to the Centers for Disease Control and Prevention, over 300,000 people in the U.S. are hospitalized every year because of pneumonia.  Certain types of pneumonia are particularly dangerous.  


S. pneumoniae can lead to the upper respiratory tract becoming infected, and the infection can spread to the lungs, blood, middle ear, and even the nervous system.  Children under the age of 5 and adults over 65 are the most likely to contract pneumococcal pneumonia, and it is easier to become re-infected once you were originally infected.  


Because of the severity of the illness, pneumonia currently ranks as the 15th leading cause of death in the U.S.  Adults over the age of 55 account for 92 percent of pneumonia deaths every year.  


The study is occurring at six National Institute of Allergy and Infectious Diseases (NIAID) vaccine and treatment units in across the county.  The following centers are conducting the study: University of Iowa, Saint Louis University, Cincinnati Children’s Hospital Medical Center—Infectious Diseases, Vanderbilt University Vaccine Research Center, Baylor College of Medicine, and the Seattle Group Health Research Institute.  


The hope is to successfully vaccinate adults who have received lower dosages of the vaccine in the last 3 to 7 years.  


Source: National Institutes of Health

Accutane Effects

Accutane Effects

What Is Accutane?
 
 
Accutane is the product name for Isotreinoin. Accutane is a medication developed by Hoffman-La Roche for acne treatment. Isotreinoin is a naturally occuring derivative of vitamin A but the drug, Accutane, involves heavy doses of isotreinoin and is used to treat severe and scarring types of acne. Other uses for Accutane include treatment for some forms of cancer and for some severe skin conditions.
 
 
What Are The Side Effects?
 
 
The common side effects of Accutane use include lips, dry skin, nosebleeding, joint and muscle pains and temporary hair thinning. Although these are considered to be the most common of the side effects attributable to Accutane, the most dangerous side effects attributable to the drug are inflammatory bowel disease, depression and birth defects. Although these cases are rare, they have proven to have long-term, disastrous results.
 
 
INFLAMMATORY BOWEL DISEASE
 
 
Inflammatory bowel disease is the name for a common group of ailments that cause reddening and swelling of the intestines. Inflammatory bowel disease comes in two major forms, Crohn's disease and Ulcerative Colitis. Crohn's disease usually causes open sores along the length of the small and large intestines. Ulcerative colitis causes ulcers in the lower part of the large intestine. Both Crohn's disease and Ulcerative colitis can damage the rectum and in some cases cause rectal cancer.
 
 
The symptoms of ulcerative colitis is a loosening of the stool which will be bloody and associated with severe abdominal pain. Ulcerative colitis is also characterized by skin lesions and pain in joints. The symptoms of Crohn's disease are very similar and about 10% of all cases are unable to be distinguished as ulcerative colitis or Crohn's disease.
 
 
BIRTH DEFECTS
 
 
Within months of Accutane being released onto the market there were signs of birth defects resulting from exposure. Exposure to the drug by pregnant women has resulted in birth defects similar to those seen in Thalidomide. Even minor amounts of Accutane that reach a fetus can result in numerous abnormalities. Excessive spontaneous abortions have been attributed to the drug as well as numerous birth defects including skull and ear abnormalities, faial dysmorphia, cleft palate, cerebral abnormalities and cardiovascular abnormalities.
 
 
GOVERNMENT REGULATIONS
 
 
Over concern for the great risk of deformaties associated with the use of Accutane amongst pregnant women the government has been fully involved with attempting to regulate Accutane exposure. In 1988 the government attempted to regulate Accutane after it was discovered that physicians were overprescribing Accutane and in some cases prescribing the drug to pregnant women. The idea behind the regulation was to have physicians more informed about the drug and possibly only allow certain physicians to prescribe the drug. This regulation did not pass but as a result of government intervention the warning labels for the drug were required to be twice the normal size and have a picture of a fetus. In 2002 the government finally created an initiative called iPLEDGE that requires physicians to get extensive training on the administration of the drug. In 2009, due to extensive lawsuits Hoffman-La Roche discontinued the production of Accutane.
 
 
LAWSUITS
 
 
Lawsuits involving Accutane have become commonplace in recent years. As of 2011 there are 4,000 plaintiffs awaiting trial to sue Hoffman La-Roche for various conditions resulting from the use of the drug. Recent cases have resulted in a $2.6 million dollar verdict for a New Jersey resident who had to have his colon removed due to Accutane induced irritable bowel disease. A $2.2 million dollar verdict for a woman whose baby was born with severe heart and brain disease. A case involving actor James Marshal, which began in February, contends that his acting career was destroyed due to Irritable Bowel Syndrome caused by the drug.
 
 
What to do if I have illness due to Accutane exposure
 
 
If you or someone you know has been exposed to Accutane and have developed any conditions associated with the drug or have had a child born with birth defects after taking the drug Accutane you should immediately consult a physician. If the diagnosis involves Irritable Bowel Disease, Crohn's Disease, Ulcerative Colitis, Depression, Birth Defects or any other conditions associated with Accutane you should consult a personal injury attorney familiar with Accutane class actions lawsuits. The timeliness of a claim for this stems from a number of factors including jurisdiction, when you started Accutane and when your symptoms began. For this reason it is important to get the appropriate legal advice.
 

What is Celebrex Used For

What is Celebrex Used For


A brief guide to Celebrex uses

The prescription medication Celebrex is primarily designed to provide pain relief. When researching what is Celebrex used for, you will find that it’s most common applications include treatment of pain in menstruating women, people with arthritis and those with colon polyps. Celebrex uses can be helpful in controlling pain but also carry many side effect risks. When asking a physician what is Celebrex used for, it is important to receive a thorough briefing about all adverse effects that may occur before committing to a course of treatment.

Celebrex uses control pain in arthritic patients, including making movement easier. For women who experience severe cramps during menstruation, they should be told that controlling this pain is among the potential answers to the question "What is Celebrex used for?" These forms of relief, however, can lead to more severe conditions. Physicians who prescribe the drug must make sure that serious adverse effects do not dilute Celebrex uses.

When asking "What is Celebrex used for?" you should provide doctors with a thorough description of your medical history. Patients who have had cardiac trouble are at increased risk for heart attack and stroke despite Celebrex uses that are otherwise beneficial. A doctor should be ready to explain in response to "What is Celebrex used for?" that the medication also can create ulcers or internal bleeding in patients.

It is important to monitor yourself for any signs that Celebrex uses will cause you more harm than good. During your first ingestion of the drug, be alert to any indication that you have an allergic reaction to the medication. During their explanation concerning what is Celebrex used for, a doctor will explain that difficulty breathing, developing skin rashes and facial swelling all indicate a need for immediate medical attention.

Never take the drug without a physician's supervision. Even if you conclude that Celebrex uses can alleviate your condition, do not attempt to order the medication from an online pharmacy without a prescription. Though you may independently decide that you have satisfactorily researched what is Celebrex used for, you are not capable of creating a suitable dosage for yourself. Attempting to take advantage of Celebrex uses with an illegal drug purchase also places you at legal risk of being prosecuted for such a transaction.

After receiving a physician's explanation of what is Celebrex used for, conduct further research by reading the prescription information. This has been provided by the manufacturer outline and goes into extensive detail about potential side effects. By offering this documentation concerning the potential adverse reactions that go along with Celebrex uses, the manufacturer protects itself against litigation alleging they have misled consumers, resulting in serious health damage.

If you follow a doctor's intake order but still experience a reaction not cautioned against by the manufacturer, you may be able to sue them for damages. Find a lawyer in your area who is knowledgeable about how to handle cases of this sort.

 

Lexapro

Lexapro

What is Lexapro?
 
 
Lexapro, generically known as Escitalopram, is an prescription based antidepressant manufactured by Forest Laboratories.  It is directed for the acute and maintanence treatment of major depressive disorder (MDD) in adults and adolescents from ages 12 -17 years old.  It is also often prescribed for generalized anxiety disorder (GAD).
 
 
What is major depressive disorder?
 
 
Major depressive disorder (MDD) entails the prominent and steady continuation of depression.  In this context "steady" means every day for at least 2 weeks.  Symptoms of MDD include depressed mood, loss of interest in activities, change in weight or appetite, insomnia or hypersomnia. 
 
 
What are the side effects associated with Lexapro?
 
 
Side effects from the use of Lexapro include: dizziness and drowsiness; sleep problems; mild nausea; weight changes; decreased sex drive and/or impotence; and dry mouth, yawning, and ringing in your ears.  More serious side effects include:  very stiff muscles, high fever, sweating, fast or uneven heartbeats, tremors, overactive reflexes; nausea, vomiting, diarrhea, loss of appetite and loss of coordination; headache, trouble concentrating, memory problems, weakness, confusion, hallucinations, fainting, seizure and shallow breathing.  If you have any of these major symptoms it is important that you go call your doctor immediately.
 
 
One of the most serious side effects of Lexapro use is the creation of birth defects in children born to women who used Lexapro during pregnancy.  One of the major birth defects is known as Truncus Arteriosis.  This is a condition that develops in the fetus where the major arteries that lead out of the ventricles of the heart combine together.  This causes the mixing of oxygenated and de-oxygenated blood resulting in shortness of breath and a relatively low oxygen level in the blood.  If it is not treated within a year of birth the results are often fatal.
 
 
Government Regulations
 
 
In 2004 the FDA, after reviewing newly available information, declared that a warning to physician's about prescribing Lexapro to women who are in their third trimester of pregnancy.  The warning went so far as to state that physician's who are prescribing Lexapro to their patients should ween them off the drug.
 
 
In 2006 the FDA issued a safety alert for Lexapro and other drugs categorized as SSRI's, including Paxil and Prozac.  The safety alert warned of evidence that exposure to Lexapro during pregnancy can increase the risk of Persistent Pulmonary Hypertension in children after birth.
 
 
Lawsuits
 
 
As of September 2011 there are no pending or settled class action lawsuits involving Lexapro.  However, due to a number of birth defects that have been attributed to the use of Lexapro by pregnant women the possibility of class action lawsuits being filed is very predictable. 
 
 
What to do if exposed to Lexapro?
 
 
If you were exposed to Lexapro and subsequently had a child with birth defects, especially Truncus Arteriosis, it is important that you contact an attorney who specializes in class actions of this type.  Cases are beginning to take form and you may have a case, especially if you were not warned about possible side effects.

Advair 250 50 Side Effects

Advair 250 50 Side Effects

A brief guide to Advair Diskus 250 50 side Effects

All prescription medications carry the risk of mild or severe side effects, and Advair Diskus is no exception. Potential Advair 250 50 side effects must be elucidated by a physician before assigning a course of treatment to patients with asthma or chronic obstructive pulmonary disorders (COPD).

The presences of Advair Diskus 250 50 side effects are rare. If you experience any adverse reactions as a result of Advair use, you must immediately contact your medical provider and/or doctor. Depending on the severity of the reaction, your doctor may advise you to discontinue use.
Children who are prescribed this medication are at greater risk of Advair 250 50 side effects, particularly ear and throat infections.

Allergic reactions to Advair may occur shortly after the onset of treatment. Advair 250 50 side effects including rashes, hives and inflammations around the mouth should be immediately reported to your doctor.

Trouble breathing is one of the most serious Advair Diskus 250 50 side effects. If experienced, you must immediately use your emergency respirator. If this does not resolve the Advair 250 50 side effects, seek emergency treatment.

As stated above, it is necessary to report all Advair side effects to your medical professional. Only a qualified doctor is permitted to evaluate whether your adverse effects are severe enough to justify a cessation of treatment. If a physician fails to take adequate measures to ensure the health of patients, they may be guilty of negligence. Should serious Advair 250 50 side effects ensue after beginning treatment, you may decide to consult with a lawyer to see whether your doctor can be successfully sued for malpractice. Before filing a case, be sure to assemble all prescriptions and medical records to provide suitable information for a case.

 

Advair Diskus

Advair Diskus

A Brief Overview of Advair Diskus

For patients (ages four and up) who suffer from asthma, the prescription medication Advair Diskus can be issued if their current medication is not sufficient to control their condition. While there is no maximum period for how long its use can be continued, this drug is not intended for indefinite long-term use–continued use of Advair Diskus can endanger patient health in significant ways, up to and including potential death. To avoid adverse effects, physician guidelines must be followed and any adverse effects must be immediately reported.

Advair Diskus is an inhalant drug whose dosage varies with the age of the patient and the severity of their condition. Dosage can take the form of 100 micrograms, 250 micrograms or 500 micrograms a day. Regardless of age, patients begin taking the drug in the form of 100 micrograms taken twice daily. After observing how the patient's symptoms respond to Advair Diskus, a physician may increase the regimen as they deem appropriate.

The drug is meant to be taken in combination with a long-term asthma condition. Once symptoms have been contained or alleviated, the dosage of Advair Diskus is steadily decreased and discontinued. Patients should then be able to continue to use less potentially harmful asthma control medication.

Some of the potential side effects, such as headaches and nausea, of Advair Diskus are commonly observed in prescription medications. Be alert to any sign of an immediate allergic reaction, especially rashes or other skin problems. Advair Diskus should take effect 30 minutes after inhalation, though it may take up to a week of use before this will be noticeable. However, if the drug seems to increase breathing problems or produce an irregular heartbeat, notify your physician immediately. In such cases, usage of Advair Diskus may have to be discontinued. Moreover, children under four should not be prescribed Advair; child use can impair or inhibit growth.

 In no case should the drug be used more often than prescribed by a physician for the purposes of immediate relief. Overuse and abuse of Advair Diskus creates the risk of potentially fatal consequences.

Litigation cannot be advanced by patients who disregard intake instructions. However, patients experiencing serious adverse effects despite following a physician's guidelines may have grounds for litigation against the manufacturing company. Those without legal training will not be able to successfully represent themselves, since proving a direct link between usage of Advair Diskus and adverse effects is a complicated area of the law.

If you wish to explore litigation, schedule a consultation with a lawyer in your area who specializes in this type of lawsuit. Make sure you assemble all medical records and prescription information prior to arriving to your first meeting with a lawyer.

 

Advair Diskus Inhaler

Advair Diskus Inhaler

How to use an Advair Diskus inhaler

 

 

Asthmatic patients prescribed the drug Advair Diskus must carefully follow their physician's guidelines to prevent the formation of side effects. Advair, which is administered through an inhaler, is similar in design to emergency inhalers.

 

 

When prescribing the drug, a physician will explain how to properly use an Advair disk inhaler. Intake will occur twice a day. It is recommended that you allow twelve hours to pass between the use of the Advair Diskus inhaler. Whether you have consumed food prior to intake is irrelevant.

 

 

It is important to understand that when using Advair disk inhaler, you will be receiving the drug in the form of a powder. Because of its fine texture, you may not feel any grains when you inhale from the Advair Diskus inhaler. However, this does not mean that you should use an Advair disk inhaler to take another dose, for extra doses will significantly increase the risk of adverse effects.

 

 

Following the use of an Advair Diskus inhaler, you should rinse your mouth out with water. After gargling for several seconds, spit the water out.

 

Make sure that you keep track of the counter located on the Advair Diskus inhaler. When you are down to five doses, the Advair disk inhaler will display the remaining number of doses in red. This is an indication that you must refill your prescription. Make sure to maintain your Advair Diskus inhaler in a clean and safe location where it cannot be tampered with.

 

 

While an Advair disk inhaler is similar in appearance to an emergency inhaler, it is not designed for similar use. If you experience severe symptoms, do not take an extra dose of the medication through your Advair Diskus inhaler. The drug is not intended for the immediate relief of severe symptoms. 

 

 

Some people may not be able to use an Advair disk inhaler to take the drug in a dry powder form. For patients whose breathing problems are so severe that they are unable to effectively use an Advair Diskus inhaler, a doctor may consider prescribing HFA. This is an aerosol-based form of the medication.

 

If you receive a defective or faulty Advair Diskus inhaler which leads to adverse effects, the retailer who may be held responsible in the court of law. Only a lawyer experienced product liability, drugs or personal injury will be able to determine who the appropriate defendant is and whether a lawsuit is likely to obtain compensation. If you are involved in a similar situation, you should maintain copies of all receipts of sale and all medical documents to affirm your case.