Fosamax Attorney and Lawyer – How to Hire

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Fosamax Attorney and Lawyer – How to Hire

If you have developed Osteonecrosis of the Jaw (ONJ) after taking Fosamax, you may be entitled to recover damages from the manufacturer, distributor, or physician who prescribed the drug for you. To find out if you have a claim, contact a qualified Fosamax attorney who can evaluate your case as soon as possible. All states set time limits for filing lawsuits, including your state. If you don’t file your Fosamax lawsuit within that time limit (called the statute of limitations), you’ll lose any claim you might have had, no matter how serious an injury you have suffered. If you have a good Fosamax lawsuit, your Fosamax lawyer can tell you which parties you should name as defendants and the jurisdiction where you should file your case.
It’s never a good idea to try and handle this kind of litigation on your own or to be represented by an inexperienced attorney. Large pharmaceutical companies like Merck, the manufacturer of Fosamax, have very experienced defense attorneys who know how to conduct pharmaceutical litigation. This is a very specialized area of law where you want to have a knowledgeable and qualified Fosamax attorney representing you.
Suffered harm from Fosamax? You may have a lawsuit. Click here, for a top rated law firm to evaluate your legal rights.
So how do you find an attorney who specializes in this area? You can ask friends and business colleagues for references. If those sources don’t produce a referral, a good place to start looking is AttorneyPages.com, where you’ll find listings for drug liability specialists in your area, or post your case to the free Case Evaluation Form. After posting your case, an experienced law firm that handles Fosamax and similar cases will contact you for a free case evaluation, without any cost or obligation.
Check out the following articles for more information about Fosamax, filing a Fosamax lawsuit and finding a Fosamax attorney.
For more information about Fosamax, see Drug Overview: Fosamax Side Effects and Claims
For more information about Fosamax side effects, see Fosamax Side Effects – Osteonecrosis of the Jaw (ONJ)
To find out more about the FDA warning, see Fosamax Side Effects and Risks
For more information about Fosamax updates, see Fosamax Information and Warnings
If you would like to learn more about Fosamax lawsuits, see Fosamax Lawsuits, Litigation & Lawyers
Suffered harm from Fosamax? You may have a lawsuit. Click here, for a top rated law firm to evaluate your legal rights.

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Fosamax Class Action Lawsuits, Litigation & Lawyers – What You Should Know

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Fosamax Class Action Lawsuits, Litigation & Lawyers – What You Should Know

Fosamax, Merck’s osteoporosis drug, has been linked to Osteonecrosis of the Jaw (ONJ), a degenerative condition of the jawbone. Fosamax, and other similar drugs called bisphosphonates, accumulate in bones, particularly in the jawbone, and inhibit the bone’s natural ability to repair everyday damage.
Several Fosamax lawsuits have already been filed, and many commentators are comparing the Fosamax scandal to the heavy litigation against the same manufacturer, Merck, for its product Vioxx. The lawsuits allege that Merck knew about the potential for ONJ and did not reveal the danger to the public.
One Fosamax lawsuit has been filed by a woman in Naples, Florida, who developed infections in teeth with root canals approximately 6 months after she began taking Fosamax for osteoporosis. The teeth had to be removed and replaced by implants, but osteonecrosis developed and the jawbone in the area became exposed. It’s not yet known whether the bone will recover or have to be removed and new bone grafted.
Suffered harm from Fosamax? You may have a lawsuit. Click here, for a top rated law firm to evaluate your legal rights.
CNN reports that 15 Fosamax cases had been filed by May 2006, but others are expected. The attorney for one woman intends to seek a class action. His client suffered loss of bone in the jaw and some teeth after taking Fosamax for 9 years. Fosamax lawsuits have been filed in Florida, New York, and Tennessee.
Merck denies that Fosamax has been shown to cause ONJ, and argues that people with osteoporosis may just be more likely to develop the condition.
Check out the following articles for more information about Fosamax, filing a Fosamax lawsuit and finding a Fosamax attorney.
For more information about Fosamax, see Drug Overview: Fosamax Side Effects and Claims
For more information about Fosamax side effects, see Fosamax Side Effects – Osteonecrosis of the Jaw (ONJ)
To find out more about the FDA warning, see Fosamax Side Effects and Risks
For more information about Fosamax updates, see Fosamax Information and Warnings
To learn more about Fosamax attorneys and how to find one, see Hiring a Fosamax Attorney and Lawyer
Suffered harm from Fosamax? You may have a lawsuit. Click here, for a top rated law firm to evaluate your legal rights.

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Fosamax Information and Warning

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Fosamax Information and Warning

Fosamax, Merck’s osteoporosis and Paget’s disease drug, has been implicated as a cause of Osteonecrosis of the Jaw (ONJ) or Dead Jaw disease. ONJ is caused by the temporary or permanent loss of blood to bone tissue, which causes the tissue in the jawbone to die and the bone to decay. ONJ can also occur when the bone is prevented from replacing itself by the use of drugs like Fosamax. It has been estimated that more than 2,400 Fosamax patients have reported serious jaw problems, including ONJ, since 2001.
Fosamax is one of a group of drugs called bisphosphonates, and the jaw absorbs 10 times as much of a bisphosphonate as other bones in the body. Bisphosphonates prevent normal bone renewal, and the jaw and maxilla need renewal because they receive slight daily injuries from normal use. The continual injury and lack of renewal can lead to bone death.
The risk of bisphosphonate-related ONJ has been linked to the size of the dose, according to Maico Meol, oral surgeon at the Washington Center Hospital in Toronto, Canada. Almost 95% of bisphosphonate-related ONJ cases are related to high doses taken intravenously as chemotherapy. Bisphosphonates have a shelf life of about 12 years and stay in the body. Because they stay in the jawbone in large amounts, experts fear that many bisphosphonate-related ONJ cases will emerge in the future. ONJ is often brought on by invasive dental work, such as extractions, that injure the jawbone, but it sometimes occurs spontaneously.
Suffered harm from Fosamax? You may have a lawsuit. Click here, for a top rated law firm to evaluate your legal rights.
A report was published by Dr. Salvatore Ruggiero, a surgeon at the Long Island Jewish Hospital in 2004. He found bisphosphonate-related ONJ cases in both chemotherapy patients and those being treated from osteoporosis. An article by the head of oral and maxillofacial surgery at the University of Miami, Robert E. Marx, was published an article in the November, 2005 Journal of Oral Maxillofacial Surgery reporting bisphosphonate-related ONJ cases in patients receiving chemotherapy.
Fosamax information indicates that ONJ is a potential Fosamax side effect, particularly for patients who take it for a long period of time.
Check out the following articles for more information about Fosamax, filing a Fosamax lawsuit and finding a Fosamax attorney.
For more information about Fosamax, see Drug Overview: Fosamax Side Effects and Claims
For more information about Fosamax side effects, see Fosamax Side Effects – Osteonecrosis of the Jaw (ONJ)
To find out more about the FDA warning, see Fosamax Side Effects and Risks
If you would like to learn more about Fosamax lawsuits, see Fosamax Lawsuits, Litigation & Lawyers
To learn more about Fosamax attorneys and how to find one, see Hiring a Fosamax Attorney and Lawyer
Suffered harm from Fosamax? You may have a lawsuit. Click here, for a top rated law firm to evaluate your legal rights.

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Duragesic Patch Side Effects – Drug Overdose

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Duragesic Patch Side Effects – Drug Overdose

The Duragesic Patch, manufactured by Janssen Pharmaceutical Products, and the generic fentanyl transdermal skin patch manufactured by Mylan Laboratories and Actavis Inc., are drug delivery patches that administer doses of the potent narcotic fentanyl through the skin. The FDA (Food and Drug Administration) issued a Public Advisory Warning in July 2005 announcing an investigation into the safety of pain patches after 120 deaths were linked to fentanyl patch use.

Suffered harm from Duragesic Pain Patch? You may have a lawsuit. Click here, for a top rated law firm to evaluate your legal rights.

Fentanyl is a narcotic drug, said to be up to 100 times as strong as morphine, and an overdose can cause death. The symptoms of a fentanyl overdose include:

Trouble breathing or shallow breathing

Loss of consciousness or coma

Seizures

Cold and clammy skin

Small pupils

Tiredness

Extreme sleepiness or sedation

Confusion

Inability to function normally

Faintness

Dizziness

Overdoses of fentanyl that are not fatal can cause damage to the cardiovascular system (bradycardia) and to the central nervous system. Continued exposure to high doses can lead to dependency and narcotic addiction.

If you or a family member have been prescribed a Duragesic or generic pain patch, you should consult with your health care provider about how to avoid overdoses and be very careful not to use damaged patches or old patches that might have been on the recall list for leaking patches.
In 2007 the FDA issued an additional alert about fentanyl patches, giving the following advice: :

The fentanyl patch should only be used by patients who are opioid-tolerant and have chronic pain that is not well controlled with other pain medicines.

Healthcare professionals who prescribe and patients who use the fentanyl patch should be aware of the signs of fentanyl overdose.

Patients prescribed the fentanyl patch should tell their doctor about all the medicines that they take to avoid dangerous interactions.

Patients and their caregivers should be told how to use the fentanyl patch.

Heat may increase the amount of fentanyl that reaches the blood and can cause life-threatening breathing problems and death.

If you use fentanyl patches take them out of the package with protective gloves on and examine them carefully for leaks, flaws, or variations in size. If you have any doubts about a patch, do not use it.

If you or a loved one have been injured or a family member has died after using a Duragesic Patch or generic pain patch, you may be able to recover damages. See Hiring a Duragesic Patch Attorney for information on finding a Duragesic Patch lawyer who can evaluate your case.

Check out the following articles for more information about Duragesic Patch, filing a Duragesic Patch lawsuit and finding a Duragesic Patch attorney.

For more information about Duragesic Patch, see Drug Overview: Duragesic Patch Side Effects and Claims

For more information about Duragesic Patch updates, see Duragesic Patch Information and Warnings

To find out more about the FDA warning, see Duragesic Patch Side Effects and Risks

If you would like to learn more about Duragesic Patch lawsuits, see Duragesic Patch Lawsuits, Litigation & Lawyers

To learn more about Duragesic Patch attorneys and how to find one, see Hiring a Duragesic Patch Attorney and Lawyer

Suffered harm from Duragesic Pain Patch? You may have a lawsuit. Click here, for a top rated law firm to evaluate your legal rights.

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Drug Overview: Duragesic Patch

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Drug Overview: Duragesic Patch

The Duragesic pain patch, manufactured by Janssen Pharmaceutical Products, is a medication delivery system intended to release the painkiller fentanyl into the skin over a period of a few days. A generic form of this patch (fentanyl transdermal skin patch) was brought out by Mylan Laboratories in 2005, and a later generic version was produced by Actavis, Inc. The Duragesic patch claim is that medication given through the skin goes directly into the bloodstream, bypassing the liver and stomach, which often means that lower doses are required. The Duragesic pain patch was approved by the FDA (Food and Drug Administration) in 1997.

Suffered harm from Duragesic Pain Patch? You may have a lawsuit. Click here, for a top rated law firm to evaluate your legal rights.

In 2004 Janssen recalled several batches of the Duragesic pain patch because of a faulty seal that can cause an overdose. More than 400,000 patches were involved in the recall. In 2008 patches marketed under the brand Duragesic by PriCara and as a generic product by Sandoz Inc. were recalled. That recall involved all 25-microgram-per-hour patches with expiration dates on or before December 2009. The patches were recalled because they might be cut and cause the gel to leak onto the skin of the patient or caregiver, causing serious injury or death. In 2008 Actavis Inc. recalled all its fentanyl patches with expiration dates between May 2009 and December 2009. These recalls have raised concern about whether these patches can be manufactured safely
The FDA issued a Public Health Advisory warning on July 7, 2005, saying that the FDA is investigating reports of death and other serious side effects from overdoses of the narcotic fentanyl in fentanyl transdermal skin patches.

Reports indicate that not only faulty seal, but factors such as heat, exercise, and fever can alter the dosage of narcotic released by these patches. Fentanyl, a drug up to 100 times more potent than morphine, is dangerous in high doses. See Duragesic Patch Information and Warnings for more information. The FDA has announced that at least 120 deaths have been linked to use of fentanyl patches.
In 2007 the FDA issued an additional safety warning.

Check out the following articles for more information about Duragesic Patch, filing a Duragesic Patch lawsuit and finding Duragesic Patch attorney.

For more information about Duragesic Patch side effects, see Duragesic Patch Side Effects

For more information about Duragesic Patch updates, see Duragesic Patch Information and Warnings

To find out more about the FDA warning, see Duragesic Patch Side Effects and Risks

If you would like to learn more about Duragesic Patch lawsuits, see Duragesic Patch Lawsuits, Litigation & Lawyers

To learn more about Duragesic Patch attorneys and how to find one, see Hiring a Duragesic Patch Attorney and Lawyer

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Hiring A Duragesic Patch Attorney and Lawyer

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Hiring A Duragesic Patch Attorney and Lawyer

The Duragesic Patch and similar generic patches are medication delivery systems to administer doses of the powerful narcotic drug fentanyl by absorption through the skin. Faulty patches have been reported and hundreds of thousands of fentanyl patches have been recalled between 2004-2008. The release of fentanyl is also affected by heat. Fentanyl patches have been linked with at least 120 deaths from overdoses.

Suffered harm from Duragesic Pain Patch? You may have a lawsuit. Click here, for a top rated law firm to evaluate your legal rights.

If you or a close family member has suffered injury from a Duragesic Patch or generic patch, you may be able to recover damages. It will be in your best interest to contact a qualified Duragesic Patch attorney as soon as possible to evaluate your case. If you have a good case, you will need to file your lawsuit within the time specified in your state’s law. A qualified Duragesic Patch Lawyer will be able to guide your through this procedure and help you make other important decisions about which parties to name as defendants in your case and the best place to file your suit.

If you are considering trying to represent yourself in this kind of litigation, you should reconsider. In lawsuits with potential damages in the millions, large pharmaceutical companies hire very experienced pharmaceutical litigation specialists to defend them. Your best hope of recovery is to have a qualified pharmaceutical-litigation specialist of your own.

If you are having trouble finding an attorney, a good place to start is Attorneypages.com, where you’ll find listings for drug liability specialists in your area, or post your case to our Duragesic Patch case evaluation form. After posting your case, an experienced lawyer will contact you for a free case evaluation.

Check out the following articles for more information about Duragesic Patch, filing a Duragesic Patch lawsuit and finding a Duragesic Patch attorney.

For more information about Duragesic Patch, see Drug Overview: Duragesic Patch Side Effects and Claims

For more information about Duragesic Patch side effects, see Duragesic Patch Side Effects

For more information about Duragesic Patch updates, see Duragesic Patch Information and Warnings

To find out more about the FDA warning, see Duragesic Patch Side Effects and Risks

If you would like to learn more about Duragesic Patch lawsuits, see Duragesic Patch Lawsuits, Litigation & Lawyers

Suffered harm from Duragesic Pain Patch? You may have a lawsuit. Click here, for a top rated law firm to evaluate your legal rights.

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Duragesic Patch Lawsuits, Litigation & Lawyers

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Duragesic Patch Lawsuits, Litigation & Lawyers

Pain patches containing the narcotic fentanyl, including the Duragesic Patch manufactured by Janssen Pharmaceutical Products, have been linked to a number of deaths from overdoses of fentanyl, which can suppress the respiratory system. Some of these deaths have led to litigation.

Suffered harm from Duragesic Pain Patch? You may have a lawsuit. Click here, for a top rated law firm to evaluate your legal rights.

The mother of a 36-year-old man who died from a fentanyl overdose in 1994 won a verdict of $5 million against the manufacturer in an early Duragesic Patch lawsuit. The case was settled by a confidential agreement on appeal. Kurt Hophan had been prescribed a patch for pain from a back injury. He fell asleep with a heating pad and an electric blanket and never woke up. The heat of the pad and blanket were said to have caused the patch to release 100 times the prescribed dose of fentanyl.

A Duragesic Patch lawsuit filed in December 2005 seeks damages for the death of a 72-year-old Salt Lake area woman after use of a Duragesic Patch. This Duragesic Patch litigation was brought against the Duragesic distributor ALZA Corporation and against Janssen Pharmaceutical Products. The suit claims that the companies sold defective and leaking patches with inadequate warnings. Plaintiffs are seeking damages that include medical expenses, funeral costs, out-of-pocket expenses, loss of love, companionship and economic support, punitive damages and attorney fees.

Many other Duragesic Patch and fentanyl patch lawsuits have been filed. One Alabama firm of Duragesic Patch lawyers has announced the filing of more than 30 suits.

If you or a loved one has suffered an overdose from a Duragesic Patch or a generic fentanyl patch, you may be entitled to receive damages for your injuries. You should consult a qualified Duragesic Patch attorneyy to have your case evaluated.

Check out the following articles for more information about Duragesic Patch, filing a Duragesic Patch lawsuit and finding a Duragesic Patch attorney.

For more information about Duragesic Patch, see Drug Overview: Duragesic Patch Side Effects and Claims

For more information about Duragesic Patch side effects, see Duragesic Patch Side Effects

For more information about Duragesic Patch updates, see Duragesic Patch Information and Warnings

To find out more about the FDA warning, see Duragesic Patch Side Effects and Risks

To learn more about Duragesic Patch attorneys and how to find one, see Hiring a Duragesic Patch Attorney and Lawyer

Suffered harm from Duragesic Pain Patch? You may have a lawsuit. Click here, for a top rated law firm to evaluate your legal rights.

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Duragesic Patch Information and Warnings

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Duragesic Patch Information and Warnings

The FDA (Food and Drug Administration) issued a Public Advisory warning in July 2005, announcing a study into the safety of pain patches after reports of at least 120 deaths from drug overdoses. The Duragesic pain patch, manufactured by Janssen Pharmaceutical Products, and generic patches manufactured by Mylan Laboratories and Actavis Inc., all deliver the narcotic fentanyl through the skin to patients with severe and chronic pain.

Suffered harm from Duragesic Pain Patch? You may have a lawsuit. Click here, for a top rated law firm to evaluate your legal rights.

Fentanyl, a drug that is up to 100 times stronger than morphine with effects similar to heroin, is held in a gel in the pain patch and is supposed to be released in controlled doses into the patient’s bloodstream by absorption through the skin. If the wrong dose is administered, the patient can suffer an overdose that may be fatal.

A new patient package insert for Duragesic pain patches was released with the 2005 FDA warning. It includes the following warnings:

Duragesic can cause serious and possibly fatal side effects.

Duragesic should only be used by patients with chronic pain who are already using narcotic medicines.

Duragesic should not be used for short-term pain.

Only patients who are opoid tolerant should use Duragesic. Patients should check with their doctors to find out if they are.

Duragesic should not be used by children under 2, and only by patients who are already taking opoid medications.

Never use a patch that is open or damaged in any way. This could result in a fatal overdose.
A similar warning was given again in 2007.

Check out the following articles for more information about the Duragesic Patch, filing a Duragesic Patch lawsuit and finding a Duragesic Patch attorney.

For more information about Duragesic Patch, see Drug Overview: Duragesic Patch Side Effects and Claims

For more information about Duragesic Patch side effects, see Duragesic Patch Side Effects

For more information about Duragesic Patch updates, see Duragesic Patch Information and Warnings

If you would like to learn more about Duragesic Patch lawsuits, see Duragesic Patch Lawsuits, Litigation & Lawyers

To learn more about Duragesic Patch attorneys and how to find one, see Hiring a Duragesic Patch Attorney and Lawyer

Suffered harm from Duragesic Pain Patch? You may have a lawsuit. Click here, for a top rated law firm to evaluate your legal rights.

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Duragesic Patch Information and Warnings

Duragestic Patch Information Drug Toxic Chemicals

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Duragesic Patch Information and Warnings

The Duragesic Patch and generic fentanyl patches release the narcotic fentanyl in measured doses through the skin for treatment of very serious and chronic pain. The Duragesic patch is manufactured by Janssen Pharmaceutical Products, and a generic forms of the product are manufactured by Mylan Laboratories and Actavis Inc.

Suffered harm from Duragesic Pain Patch? You may have a lawsuit. Click here, for a top rated law firm to evaluate your legal rights.

The FDA (Food and Drug Administration) issued a Public Advisory warning in July 2005, announcing the FDA’s intention to study the safety of the patch delivery system for the potent narcotic, fentanyl. The FDA had received at least 120 reports of deaths linked to the use of fentanyl patches.

The Institute for Safe Medication Practices, an industry watchdog group, claims that heat increases the absorption of medication from patches and exercise, a hot bath, high fever, or a heating pad or electric blanket can lead to fatal overdoses. Studies on transdermal patch delivery done at the Center for Biomaterials at Rutgers University support these claims, according to Bozena B. Michniak, a researcher there. Apparently the effect of heat on dosage levels was reported in studies as early as 1986, but users were not warned until 1994. The FDA issued a warning about this in 2007. See Duragesic Patch Side Effects – Drug Overdose for details.

There have been several recalls of both Duragesic and generic fentanyl patches. Janssen recalled hundreds of thousands of Duragesic patches in 2004 due to a faulty seal that could deliver an overdose to a patient. There were two more recalls in 2008 for Duragesic patches marketed by PriCara and as a generic product by Sandoz Inc. That recall was because the patches might be cut and pose a danger of overdose for the patient or caregiver handling them. Fentanyl patches manufactured by Actavis Inc. were also recalled because of possible leaks. Some of these patches may still be in circulation.

If you are prescribed Duragesic pain patches, make sure that the patches you receive were not included in any recall. Handle all patches with protective gloves while you examine them for defects. Discuss the risks of overdose with your health care practitioner and be sure not to subject the patches to any unusual level of heat. Find out from your health care practitioner if you should remove the patch when you are running a fever or engaging in any activity. Be aware of the signs of overdose and what you should do if you suspect that you have received an overdose.

If you or a family member have suffered serious injury or a family member has died after using a Duragesic pain patch or generic product, you may be able to make a claim for damages. You should contact a qualified Duragesic pain patch attorney to evaluate your case.

Check out the following articles for more information about Duragesic Patch, filing a Duragesic Patch lawsuit and finding a Duragesic Patch attorney.

For more information about Duragesic Patch, see Drug Overview: Duragesic Patch Side Effects and Claims

For more information about Duragesic Patch side effects, see Duragesic Patch Side Effects

To find out more about the FDA warning, see Duragesic Patch Side Effects and Risks

If you would like to learn more about Duragesic Patch lawsuits, see Duragesic Patch Lawsuits, Litigation & Lawyers

To learn more about Duragesic Patch attorneys and how to find one, see Hiring a Duragesic Patch Attorney and Lawyer

Suffered harm from Duragesic Pain Patch? You may have a lawsuit. Click here, for a top rated law firm to evaluate your legal rights.

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Accutane Side Effects and Risks

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Accutane Side Effects and Risks

Accutane, a synthetic form of vitamin A with the generic name isotretinoin, has been the subject of numerous warnings by both the FDA (Food and Drug Administration) and consumer advocacy groups.
Suffered harm from Accutane? You may have a lawsuit. Click here, for a top rated law firm to evaluate your legal rights.
The FDA first required the manufacturer of Accutane to increase warnings about the danger of birth defects as a result of using Accutane in 1983.
In the August 12, 2005 announcement the FDA said it had also approved new warnings for risks of depression and psychiatric problems. The FDA had already issued a MedWatch warning on November 1, 2002 saying that “aggressive and/or violent behaviors have been added to the list of events that Accutane may cause.” The first warnings about possible psychiatric Accutane side effects were made in 1985.
More recently Accutane has been linked to incidents of severe pancreatitis and inflammatory bowel disease, sometimes requiring surgical removal of some organs. Current Accutane warnings include all of these conditions and side effects.
If you are thinking about using Accutane be sure talk to your health care provider about all the possible side effects and learn about possible symptoms of side effects so that you and your health care provider can monitor your health. If you or a loved one have been injured or a family member died as a result of taking Accutane, you may be able to recover damages. See Hiring An Accutane Attorney and Lawyer for information about finding someone to evaluate your case.
Check out the following articles for more information about Accutane, filing an Accutane lawsuit and finding an Accutane attorney.
For more information about Accutane, see Drug Overview: Accutane Side Effects and Claims.
For more information about Accutane side effects, see Accutane Side Effects – Inflammatory Bowel Disease, Suicide & Birth Defects .
If you would like to learn more about Accutane lawsuits, see Accutane Lawsuits, Litigation & Lawyers.
To learn more about Accutane attorneys and how to find one, see Hiring an Accutane Attorney and Lawyer
Suffered harm from Accutane? You may have a lawsuit. Click here, for a top rated law firm to evaluate your legal rights.

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