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Advair Strengths

Advair Strengths

 
What are Advair strengths?
 
 
Advair strengths include reducing inflammation and irritation in the airways.  This is important in the management of asthmatic symptoms prior to attacks or just in everyday activity.  Advair effects include stopping wheezing and helping patients to breathe better, though this depends very heavily on the patient and their receptiveness to the medication.
 
 
How do I maximize the Advair strengths?
 
 
To get the maximum Advair effects, it needs to be used daily, rather than when one feels the symptoms.  You have to follow the dosing instructions as well.  While some might be instructed to take the medication once a day, the typical dosage of this drug for maximum Advair effects is twice a day, twelve hours apart.  Though you do not clean the inhaler, you should rise out afterward to remove residual medication as there are no benefic Advair effects to having the medication in the mouth.
 
 
Can I use a quick relief inhaler to maximize Advair strengths?
 
 
The instructions for Advair effects state that the use of a quick-relief inhaler is redundant and therefore should only be used in an emergency.  The doctor’s dosing instructions will better qualify what this means and when you can use the quick-relief inhaler.
 
 
To ensure you get the maximum Advair strengths as well as avoid overdoses and other issues, you will need to disclose all inhalers and other medications used to the doctor.  Never use new medications without first consulting with the doctor for warnings and other possible Advair effects applicable to your health situation.  Some medication ns must be taken to avoid unnecessary withdrawal or other premature reactions, but only the doctor can determine which Advair effects are applicable and what else must be done to your dosing regimen.
 
 
When should I consider Advair?
 
 
If you have chronic issues with breathing related to asthma, then the Advair strengths are applicable to you and you should explore your options with the doctor.  The doctor will ask you about the medications you are taking as well as run some necessary tests.  You will proceed to take a prescription written for Advair to a trusted pharmacy.  If you seek an Advair coupon, go directly to the manufacturer or drug’s website.  No other source has a reliable discount that will be accepted.  In generally, there are no free samples, but you can commit to try the drug for thirty days under some arrangements with the manufacturer, as long as one has a prescription to have the medicine dispensed by a pharmacy.
 
 
Advair is also prescribed for chronic bronchitis and other lung diseases, but the doctor will need to review patient's medical history before this course of action can be taken.
 
 
Do I have a cheaper alternative to Advair strengths?
 
 
There is no approved generic for Advair as the company still holds the applicable patent.  Until that time you must work with coupons when made available by the manufacturer to afford this medication.
 
 

Serzone

Serzone

 
Dangerous Drug Facts: Serzone (Nefazodone)
 
 
For what is Serzone (Nefazodone) used?
 
 
Serzone’s main purpose is to treat depression, and like other antidepressants, is used to balance certain chemicals in the brain like serotonin, norepinephrine, dopamine, and others.  Serzone is a serious and dangerous drug if used incorrectly, and this article will discuss the dangers of the drug, precautions, multiple side effects, and other important facts about the Ser.  
 
 
If you are taking Serzone and researching the drug for side affects you are experiencing, you need to contact your doctor right away.  
 
 
Serzone’s Dangerous Side Effects
 
 
During the testing of Ser. in clinical study, a small number of children, teenagers, and young adults up to 24 years old started to become suicidal. The suicidal thoughts associated with Serzone’s use normally appear around the start of taking the medication, and effects can also typically appear when a patient changes doses.  
 
 
If you have any of the following symptoms while taking Ser., you need to tell a family member and contact your doctor immediately: 
 
 
New or worsening depression
 
 
Thoughts of harming or even killing yourself
 
 
Extreme worry
 
 
Agitation
 
 
Panic attacks 
 
 
Difficulty falling asleep or staying asleep
 
 
Aggressive behavior 
 
 
acting without thinking
 
 
Erratic excitement 
 
 
You need to discuss family history with depression, bipolar disorder, or any other type of mental illness with your doctor before they can prescribe Serzone.  
 
 
Other Precautions to Serzone
 
 
Apart from talking about family history for mental illness, you also need to take other precautions with your doctor before trying Ser.  Some precautions before taking Serzone are listed below: 
 
 
tell your doctor if you’ve experienced one of Serzone’s (Nefozodone) allergic reactions, an allergic reaction to trazodone (Desyrel), or even any other medications
 
 
If you’re taking astemizole, carbamazepine, cisapride, pimozide, terfenadine, or triazolam, your doctor will usually avoid prescribing Serzone
 
 
tell your doctor of ALL prescription and nonprescription medications you’ve taken or all herbal products you planning on taking along with Serzone’s prescription
 
 
tell the doctor if you’ve had a history of seizures, heart attacks, chest pain, stroke, or any other type of heart disease
 
 
tell your doctor if you are pregnant, plan to become pregnant, or are breast feeding, and if you become pregnant while taking Ser., you need to call your doctor right away
 
 
If you are having surgery, tell the surgeon or dentist you are taking Ser. 
 
 
avoid driving machinery when starting the medication because Serzone’s effects can make you drowsy or affect your motor skills in some cases
 
 
avoid drinking any amounts of alcohol while taking Ser., as the combination of these drugs can become dangerous and even deadly in some cases
 
 
if you have just started the medication, Serzone’s effects can cause dizziness, lightheadedness, and even fainting if you stand up too quickly after lying down—try getting out of bed slowly while taking Ser. 
 
 
notify your doctor if you start experiencing any diarrhea, vomiting, or dehydration, as these symptoms with Serzone can cause a drop in blood pressure
 
 
Side Effects Associated with Serzone’s Use
 
 
Serzone’s use can cause mild and serious side effects in some cases, even if you are taking the medication exactly as prescribed by the doctor.  Some common side effects associated with Ser. that may become serious (in which you should notify your doctor) include: 
 
 
Headache
 
Difficulty concentrating
 
Dry mouth
 
Heartburn
 
flushing or feeling warm
 
Pain, burning, numbness, or tingling in hands or feet
 
Constipation
 
 
More serious side effects associated with Ser. include the following: 
 
 
Rash
 
hives
 
itching
 
Difficulty breathing or swallowing
 
swelling of the face, throat, tongue, lips, eye, hands, feet, ankles, or lower legs
 
Hoarseness 
 
Slow heartbeat 
 
Memory problems
 
Blurred vision or vision changes
 
Confusion
 
Seizures
 
Painful erection lasting more than 4 hours
 
 
Serzone’s use can cause multiple other minor and serious side effects, and you need to contact your doctor immediately if you experience any abnormal changes while taking this medication.  If you have a new severe allergic reaction to Serzone, your doctor may submit a report to the Food and Drug Administration’s (FDA) MedWatch Adverse Event Reporting Program to educate the public about other effects associated with Ser. 
 
 
How am I Supposed to Use Serzone (Nefazodone)?
 
 
The pill is taken by mouth around the same times every day.  Serzone’s frequency is usually twice a day, but your doctor may start you on a very low dose that will be taken only once a week and gradually increase in dose.  
 
 
Oppositely, if your doctor wants you to stop taking Serzone, they will usually decrease the dose slowly so there are not dramatic changes.  If you are feeling better after taking Serzone, you should never stop taking the medication, and you should follow all directions from your doctor and the information packet that comes with the medication.  If you have any questions about Serzone’s use, ask your doctor.  
 
 
What should I do if I forget to take a dose of Serzone?
 
 
If you have forgotten to take the medication, you should take the dose of Ser. as soon as you remember—unless it is almost time for your next dose.  If it’s close to your next dose, skip the missed dose and start your regular schedule, and DO NOT EVER take two doses of Ser. 
 
 
Signs and Steps for Suspected Overdose
 
 
If you know some that has been taking the medication or a related medication for Serzone’s purposes, you need to call the local poison control center at (800) 222-1222.  If the victim suspected of overdosing from Serzone’s use is collapsed or not breathing, you need to call the local emergency services at 911.  Common symptoms of Ser. include nausea, vomiting, drowsiness, and lack of response from the victim.  
 
 
If you have any other questions about this drug, ask your doctor or pharmacist.  Don’t ever abuse this medication, and never give the medication to another person.  Abusing prescriptions is a felony!
 
 

Symbyax

Symbyax

 
Dangerous Drug Facts: Symbyax
 
 
Common Uses of Symbyax
 
 
Symbyax’s (Olazapine and Fluoxetine HCI Capsules) uses include treatment of treatment-resistant (TRD) and bipolar I depression in adults.  Symbyax was first developed to treat bipolar I depression, and the Food and Drug Administration (FDA) later approved the medication for treatment with TRD.
 
 
Treatment-resistant depression is defined as a major depressive disorder in adults who do not respond to 2 or more separate trials of different antidepressants in significant doses and duration.  Symbyax’s release on the market has helped numerous individuals, but the drug has also shown serious and sometimes fatal side effects. 
 
 
If you are experiencing any of the side effects listed within this article associated with Symbyax’s use, you need to tell a family member and contact your doctor right away.  
 
 
Dangerous Side Effects of Symbyax
 
 
Antidepressants like Sym. have been known to increase thoughts of suicide and similar behavior in children, teens, and young adults.  Sym is prescribed to adults, but if you or anyone you know show signs of new or worsening depression symptoms, unusual changes in behavior, or thoughts or suicide, you need to contact a doctor immediately.  
 
 
The symptoms associated with Symbyax’s use may appear more frequently during the first couple of months of treatment or if the dose amount is changed by a physician.  Sym. is not prescribed to child or adolescents because of its high correlation with increased suicidal thoughts, and the medication is not prescribed to elderly patients with dementia-related psychosis.  
 
 
What should I discuss with my doctor before taking Symbyax?
 
 
Your doctor will review your medical history and past medications when thinking about prescribing Sym.  You should never take Symbyax if you’ve taken a Monoamine Oxidase Inhibitor (MAOI) in the last two weeks, and you should never take an MAOI within 5 weeks of stopping Sym.  The side effects associated with Symbyax’s use and a MAOI at the same time can be serious and deadly.  
 
 
Your doctor will not prescribe Sym. if you’ve already take Mellaril (thioridazine) or the antipsychotic medicine pimozide (Orap).  Additionally, your doctor will not prescribe Sym. if you take any olanzapines liked Zyprexa, Zyprexa Relprew, or Zyprexa Zydis or take any fluoxetine hydrochlorides like Prozac, Prozac Weekly, or Sarafem.  You should also discuss all other prescription and over-the-counter drugs (including herbs) you take while discussing Symbyax’s use with your doctor.  
 
 
Additionally, you’ll want to discuss any health concerns you’ve had in the past or may have in the future before taking Symbyax.  Your doctor may avoid prescribing Sym. if any of the following conditions apply: 
 
 
Heart problems
 
Seizures
 
Diabetes or high blood sugar levels
 
High cholesterol or triglyceride levels
 
Liver problems
 
Low or high blood pressure
 
 
Strokes or “mini-strokes”
 
bleeding problems 
 
Alzheimer’s disease or family history
 
Narrow-angle glaucoma
 
Enlarged prostate 
 
Bowel obstruction
 
Breast cancer
 
Plans to become pregnant or if you are already pregnant 
 
 
Common Side Effects Associated with Symbyax
 
 
Symbyax’s use can cause common side effects, and a doctor will only prescribe Sym. if they believe the positive benefits of the medication outweigh the negative effects.  A doctor will usually start a patient out with a small dose of Symbyax and gradually work them up to a normal dose of 3mg/25mg, 6mg/25 mg, 6mg/50mg, 12mg/25mg, or 12mg/50mg of olanzapine/fluoxetine.  
 
 
Side effects may increase or decrease depending on Symbax’s dose amount, and some common side effects associated with the drug include the following: 
 
 
Tiredness 
 
feeling weak
 
increased appetite 
 
sleep for long periods of time
 
blurred vision
 
Tremors or shakes
 
Dry mouth
 
swelling of the hands and feet
 
 
There are other side effects associated with Symbyax’s use, and you’ll want to read the information packet that comes along with your medication in order to identify related side effects in the future.  
 
 
Other Serious and Dangerous Side Effects While Using Symbyax
 
 
Symbyax’s use can cause other serious side effects apart from suicidal thoughts or actions.  Most people will show no side effects while taking Sym. but others may face any of the serious side effects: 
 
 
1. High Blood Sugar (hyperglycemia) – taking Sym. will usually increase everyone’s blood sugar a bit, but having a history of diabetes can pose a serious risk to your well-being, and common signs of high blood sugar include the following: 
 
 
feeling abnormally thirsty
 
need to urinate more than usual
 
feeling very hungry
 
feeling weak or tired
 
feeling sick to the stomach
 
Feeling confused
 
Fruity smelling breath 
 
 
2. High Cholesterol and Triglycerides- Symbyax’s use can cause very high fat levels in the blood if the patient took olanzapine before they were 18
 
 
3. Increase Weight- Symbyax’s use will usually cause a person to gain some weight, and some individuals may gain more weight than others
 
 
4. Severe Allergic Reactions- Symbyax’s use can cause severe and life threatening allergic reactions, and you need to contact a doctor immediately if you experience hives or a rash, high fever and joint pain, swelling of the face, eyes, or mouth
 
 
5. Neuroleptic malignant syndrome- NMS is rare but can cause death if not treated, and you need to contact your doctor if you experience any high fever, excessive sweating, rigid muscles, confusion, or changes in breathing, heartbeat, or blood pressure while taking Symbyax
 
 
6. Tardive dyskinesia- Symbyax or coming off of Sym. can cause uncontrollable movements (especially of the face and tongue)
 
 
7. Serotonin syndrome- Symbyax’s use can cause this serious syndrome, and you need to tell your doctor if you experience any hallucinations, over-active reflexes, nausea, vomiting, or racing heart beat
 
 
8. Abnormal bleeding- Symbyax can cause unusual bleeding and bruising, especially when taken with a blood thinner, anti-inflammatory, or even aspirin 
 
 
9. Low Salt Levels- Symbyax’s use can cause hyponatremia, and you need to tell your doctor right away if you feel weak or confused, have problems concentrating, or have constant headaches
 
 
The use of Sym. can cause other serious side effects, and you need to discuss all proper side effects and precautions with your doctor before considering Symbyax.  
 
 

Zelnorm

Zelnorm

 
Is Zelnorm a Dangerous Drug?
 
 
Zelnorm, a drug known in its generic form as Tegaserod, was used in the United States and Canada for five years.  After being used for thousands of patients, Zelnorms stopped being marketed after evidence revealed they may have been more dangerous than was indicated by initial clinical tests.  If you took Zelnorm at any point while it was being sold, you may wonder what dangers the drug posed.  This guide will explain the uses of Zelnorm, its common side effects, and the dangers that took it off the market in 2007.  You'll also learn how to contact an attorney to help you if you believe Zelnorms may have injured you.
 
 
What is Zelnorm Used For?
 
 
Irritable bowel syndrome can take several forms.  While Tegaserod was used for irritable bowel syndrome, it was not for all types of IBS.  Generally, the only people who took Zelnorms were those who had constipation as their primary IBS symptom.  The drug was not used to treat Crohn's Disease or any kind of IBS or inflammatory bowel disease presenting diarrhea as its primary symptom.
 
 
Zelnorm aided IBS sufferers and people with unexplained constipation to live with significantly less discomfort and bloating.  It helps fecal matter move through the gastrointestinal tract, stimulating the reflexes that lead to bowel movements.  This helped to reduce straining and pain during bowel movements for those taking Zelnorms.
 
 
What Are the Side Effects of Zelnorm?
 
 
Zelnorms have a wide variety of side effects that users should be aware of.  The most common side effects associated with the drug include insomnia, diarrhea, headache, nausea, vomiting, joint pain, leg pain, back pain, and nasal congestion.  While these side effects may seem like they are just nuisances, there are also several more serious side effects of Zelnorm.
 
 
Allergic reactions to Zelnorms are rare but have been reported.  Patients experiencing any symptoms of an anaphylactic response including a rash, difficulty breathing, or swelling of the face or throat, may be experiencing a severe and potentially life-threatening allergic reaction.  It is important not to take Zelnorms if you have a history of allergic reactions to it or any related medications.
 
 
IBS patients who take Zelnorm to control their symptoms may be dismayed to learn that patients taking this drug required abdominal surgery, including gallbladder surgery, significantly more often than those who did not take it.  In some instances, Zelnorms can also cause an IBS sufferer to develop colitis, which leads to rectal bleeding and diarrhea.
 
 
How Serious are Reported Side Effects of Zelnorm?
 
 
While these other side effects can be quite severe for IBS sufferers, these were still not the effects that took Zelnorms off the market permanently.  Instead, new evidence showed that people who used Zelnorm were up to 10 times more likely to suffer a heart attack or stroke.  The federal Food and Drug Administration rapidly acted to stop the medication from being sold in 2007.  Canada and India quickly followed in banning the drug from pharmacy shelves.  For a brief time in 2007 and 2008, patients could still obtain Zelnorms through a special program, but this was discontinued after less than a year.
 
 
Have You Been Injured by Zelnorm?
 
 
If you have suffered from severe side effects after taking Tegaserod, you may want to consider talking to an attorney.  Dangerous drugs attorneys can make sure that you are fairly compensated for any side affects you experienced.  If you or a loved one suffered a stroke or heart attack after taking Zelnorms, you may have a case for one of these lawyers.  Often, you can use a lawsuit to get compensation not only for your economic damages (like hospital bills and compensation for missed work), but also for your pain and suffering or loss of quality of life.  Because cardiovascular events are often associated with high levels of suffering and negative impacts on life quality, these lawsuits can sometimes be quite lucrative.
 
 
If you have decided to hire an attorney, you may be overwhelmed by your options.  Web searches don't always reveal the results you want.  If you can't find what you're looking for, consider finding an attorney through a lawyer referral service.  These services are often offered by county and state bar associations, and can give your local options for legal representation.  Usually, placing a call to a lawyer referral service is free and takes just a few minutes.  You'll tell the referral clerk a little about your legal situation, and will then be referred to a lawyer in your area who takes cases like yours.
 
 
Affording a Dangerous Drugs Lawyer
 
 
Many people are scared to pick up the phone and contact a lawyer about the side effects they experienced on Zelnorm, just because they believe they will not be able to afford legal services.  The truth is, if you have been injured after taking Zelnorms, you may be able to hire an attorney even if you have no money to pay a lawyer upfront.  Often, lawyers will take dangerous drugs cases on a contingency fee basis, allowing you to pay a percentage of your settlement or jury verdict rather than a set fee.
 
 
If you sign a contingency fee agreement with your dangerous drugs attorney, you will only pay legal fees if you win.  Depending on where you're located and the complexity of your case, you can generally expect to pay 25 to 40 percent of your winnings to your lawyer.  Typically, most lawyers will charge a higher percentage rate for cases that go to trial than cases that settle out before a lawsuit can be filed.
 
 
Attorneys only accept cases on contingency if they feel they have a good chance of winning the case and collecting money.  The only way to tell if your specific case will qualify for contingency fee representation is to talk to an attorney.  When you schedule your half-hour consultation after being referred by a lawyer referral service, you can talk to your prospective attorney about fee structures and whether you qualify for this type of fee.
 
 

Zoloft

Zoloft

 
 
Is Zoloft a Dangerous Drug?
 
 
More Americans are using sertraline (brand name Zoloft) to treat their depression than ever.  As of 2007, Zolofts were taken by more Americans than any other medication in its class.  If you've been prescribed this drug, you may want to know if it has the potential to be dangerous.  If you've already experienced severe side effects, you may want to know what your legal options are and what your next steps should be.  This guide will explain how Zolofts are used and the side effects, both minor and serious, of this medication.  You'll also learn how to consult with an attorney if you've been hurt by this potentially dangerous drug.
 
 
What is Zoloft Used For?
 
 
Zolofts belong to a category of drugs called selective serotonin reuptake inhibitors.  This is the most common type of antidepressant, and drugs like Prozac and Wellbutrin are related to it.  These drugs help alleviate the symptoms of depression by changing the balance of serotonin in the brain.  Zoloft is commonly used as a substitute for tricyclic antidepressants, which can have extremely severe (and very common) side effects.
 
 
Sertraline is considered more effective than several other antidepressants in its class, and studies have shown that it can also make a positive impact on symptoms of obsessive-compulsive disorder, panic disorder, social phobias, body dysmorphic disorder, and post-traumatic stress disorder (PTSD).  Zolofts can also be used to assist women who have pre-menstrual dysphoric disorder (PMDD), a severe type of PMS that interrupts daily activities.
 
 
What Are the Side Effects of Zoloft?
 
 
Although Zolofts can be superior to other drugs in their class for treating some types of depression, their side effects can range from disconcerting to deadly.  Nearly half of patients who have been prescribed Zoloft experience sexual dysfunction, typically including a loss of sexual interest and (in men) a physical inability to achieve erection.  Orgasm dysfunction is also common, with many men and women having difficulties achieving orgasm after beginning treatment.  In rare cases, orgasm may no longer lead to pleasure and the genitals may feel numb.  These side effects may persist for years after you have stopped taking Zoloft.
 
 
Diarrhea and nausea are also common side effects, as is sweating that is unexplainable due to temperature.  Dry mouth is commonly reported, as is drowsiness, dizziness, and tremors.  Rarely, sertraline causes insomnia as well.  One unusual side effect of Zolofts is called akathisia, which consists of restlessness and inability to refrain from moving.  Unlike sexual side effects, akathisia usually stops very quickly after a patient stops taking Zoloft.
 
 
For pregnant women, taking Zolofts is a particularly dangerous proposition.  Sertraline crosses the placental barrier in the womb, exposing the developing fetus to high amounts of the chemical (up to a third of the mother's exposure).  Using Zolofts in your first trimester of pregnancy may result in birth defects including missing limbs, undeveloped anuses, and problems with the septum, which divides the baby's nostrils.
 
 
How Serious are Reported Side Effects of Zoloft?
 
 
While most side effects of Zoloft are not life-threatening, several major side effects can be deadly if patients and their doctors don't watch out for it.  Like many antidepressants, Zolofts can actually heighten suicidal ideation and increase the likelihood of a suicide attempt.  The reasons for this counterintuitive effect are still being debated, but it is important to talk to your doctor if you experience feelings of hopelessness or feel suicidal after starting to take Zoloft.
 
 
Zoloft is also potentially deadly in two specific circumstances: when patients overdose, and when they stop using the medication suddenly.  Overdoses can lead to a fast, irregular heartbeat, vomiting, and seizures.  Overdosing on this medication can be fatal, so if you believe you have taken too many Zolofts, you should contact your local Poison Control Hotline or go to the emergency room immediately.
 
 
Stopping your medication suddenly can also be very dangerous.  Intense mood swings and vivid nightmares are common when people stop taking Zoloft all at once, and some people report strange headaches or “electrical” feelings in their bodies.  These side effects can be dangerous on their own, but are even more dangerous if they trigger a major depressive episode or suicide attempt.  Anyone attempting to stop taking Zolofts should contact their doctor for a medication protocol that slowly lowers your dosage.
 
 
Have You Been Injured by Zoloft?
 
 
If you or a loved one has been hurt because they took Zolofts (including women whose babies had congenital defects as a result of sertraline use in the first trimester), you should contact a product liability attorney as soon as possible.  Some product liability attorneys specialize in suing companies that manufacture and sell dangerous drugs like Zoloft.  You may be eligible to receive compensation for your economic damages, as well as your pain and suffering and loss of enjoyment of life.
 
 
One of the best ways to find an attorney to take this kind of case in your area is to talk to your local bar association's lawyer referral service.  Often, these services can link you for free to an attorney in your area who can take your case.  You'll tell the referral service what issues you have had and why you need a lawyer, and will be referred to attorneys who specialize in cases like yours.  Usually, this process takes only a few minutes, and can save you time instead of doing long web searches that fail to yield a lot of useful information.
 
 
Initially, you'll schedule a half-hour consultation with the attorney you are referred to.  This consultation is generally free or very low cost, and allows you to get a feel for the lawyer before committing to hiring them for your case.  You can ask any questions you like during this consultation, and even if you don't hire the attorney you speak with, they are obligated to keep your information confidential.  Make sure to bring all documentation relating to your Zoloft prescription, as well as information about your injury, to your initial consultation.
 
 

Zometa

Zometa

 
 
Frequently Asked Questions about Zometa
 
 
What is Zometa?
 
 
Zometa is a type of zoledronic acid which doctors prescribe for certain cancer patients who are suffering from high levels of calcium in their bloodstream. It might also be prescribed, in cases of multiple myeloma or types of cancer which spreads to the bones from another part of the body, to treat bone damage. Since Zometa is not a form of chemotherapy, it cannot stop a cancerous tumor from growing. In those instances in which it performs successfully, Zometa increases bone density, in the process slowing the breakdown of bone and the resulting emission of calcium into the bloodstream.
 
 
How is Zometa taken?
 
 
Zometa is administered intravenously, which means that a healthcare professional will have to inject it into a patient’s veins. This process usually lasts at least fifteen minutes, and the particular dosage level is based both on the apparent effectiveness of the drug and the patient’s risks for side-effects, such as the presence of a kidney condition.
 
 
Doctors usually prescribe Zometa sessions once every three or four weeks, and they won’t be sure how the previous treatment went until at least one week afterward, since this is the amount of time needed for the drug to take its full effect. Patients usually take calcium and vitamin D supplements while undergoing Zometa treatment in order to facilitate bone regrowth.
 
 
What are the common side effects of Zometa?
 
 
Most patients suffer only very minor side effects from Zometa. The most common are dizziness, headache and some flu-like symptoms. More serious side-effects include new pains in the patient’s jaw, hip, thigh, or groin, tingling or numbness anywhere in the body, and some visual blurriness or other eye problems. A change in the amount that you urinate might also be a sign of a very serious side effect, something which might result in kidney failure if not treated, so you should consult a doctor right away if you notice a change.
 
 
Are some people allergic to Zometa?
 
 
Yes, some individuals do develop an allergy to Zometa, but this is very rare. Symptoms of an allergic reaction include a rash, itching, severe dizziness, difficulty breathing, and painful itching or swelling, especially if it is in your face, mouth or throat. If you notice these symptoms, contact a medical professional right away.
 
 
Are there any more dangerous side effects of Zometa?
 
 
In recent years, Zometa as well as other bisphosphonates which work similarly such as Actonel, Boniva, Didronel, Fosamax Skelid, Aredia, and Bonefos have been linked to some very serious side effects which could potentially be deadly. Since these side effects haven’t necessarily been advertised, many individuals have taken filed lawsuits against the manufacturers of Zometa.
 
 
If you’ve suffered from one of the following conditions and are taking Zometa, then you should consult an attorney right away:
 
 
Femur Fractures: Femur fractures occur just below the hip joint and can be extremely painful. The American Society of Bone and Mineral Research found that Zometa and other bisphosphonates should rewrite their warning labels because there is a verifiable connection between these drugs and atypical femur fractures. The study that they conducted involved 310 randomly selected cases of atypical femur fracture, and in 291 of these 310 cases, the patients turned out to be taking Zometa, usually for five years or more. The FDA confirmed the findings of the Society in a report which linked bisphosphonates with atypical femur fractures for individuals who’ve taken the drug for at least four years.
 
 
Esophageal Cancer: The British Medical Journal linked bisphosphonates to cancer of the esophagus in those cases in which the bisphosphonates were taken for at least five years. The findings were that for such patients aged 60 to 70, the risk for developing cancer was 2 in 1,000 or twice the normal risk for patients aged 60 to 70. Additionally, the FDA has verified at least thirty-four cases of esophageal cancer have been caused by the use of bisphosphonates including Zometa, and an additional thirty-four cases have been found in Europe and Japan.
 
 
Severe Musculoskeletal Pain: The FDA released a press statement in January 2008 that they were worried that doctors were underestimating the linkage between bisphosphonates and severe pain in the bones, joints, or muscles. Since this pain is sometimes debilitating, it’s a very serious consequence. Although further research is needed into the risk factors for this severe musculoskeletal pain, the FDA assured the public that bisphosphonates are to blame in many cases, and the discontinued use of bisphosphonates can be seen to cause an end to the symptoms.
 
 
Osteonecrosis of the Jaw: Osteonecrosis of the Jaw is often abbreviated to ONJ or else referred to more colloquially as dead-jaw syndrome. The condition can be defined as failure of the jaw to heal after minor trauma like tooth extraction. This will cause the bone of the jaw to be exposed, which is not only a disfiguring condition but a torturously painful one as well. There is significant research to show that high doses of bisphosphonates can be linked to an increased risk for dead-jaw syndrome when the drugs are taken by cancer patients. If you’re on Zometa and feel one of the symptoms of dead-jaw syndrome, such as jaw pain, gum swelling, loose teeth, fluid draining around the guns, or an increased heaviness in your jaw, then you should report them immediately to your doctor.
 
 
What type of legal help can I get?
 
 
Patients who’ve suffered one of these very serious side effects of Zometa may be able to take legal action against the makers of Zometa. Search for a medical malpractice attorney in your area and set-up a consultation appointment during which you can tell them about the injury done to you by taking the drug Zometa. 
 
 
Any medical malpractice attorney who will take your Zometa lawsuit will work on a contingency plan. This means that they’ll only get paid a percentage of your award or settlement, so that if you don’t get an award or settlement, your attorney won’t be paid either. Contingency plans greatly cut down on the risk you take when seeking legal action.
 
 

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.