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Nuvigil Side Effects Lawsuit Attorney


The latest Drug Safety newsletter of the Irish Medicines Board released on May 15th has warned people against taking recourse to wakefulness promoting drugs, such as Nuvigil and Provigil, to treat excessive sleepiness. It has advised doctors to check heart conditions of patients using electrocardiogram and monitor blood pressure and heart beat regularly before prescribing these drugs. The IMB has also urged caution on the part of users having a history of psychosis, depression or mania.

Though the pharmaceuticals major Cephalon claims that its drug Nuvigil is an effective means to improving conditions of people having sleep apnea, narcolepsy, and shift work sleep disorder, the Side Effects Lawsuit Attorney of the drug can lead to serious health problems. Wakefulness drugs may lead to one sleep problem while solving the other. It can cause lack of sleep that leads to a number of health complications, such as insomnia, fatigue, abnormal blood pressure, and lack of appetite. We need good sleep to help us recuperate and rejuvenate after long working hours. While lack of sleep induced by the drug can impact our efficiency and create mental problems, stimulant-like armodafinil in the drug is linked to Steven’s Johnson syndrome.

FDA Warning on Nuvigil

The FDA approved the marketing of Nuvigil in 2007 only after its manufacturer Cephalon agreed to carry label warnings on it. The federal regulator made a written request to the manufacturer two months before the market introduction of the drug to have mandatory and bold label warnings about skin rash and hypersensitivity Side Effects Lawsuit Attorney. It even asked the company to submit standard safety updates highlighted during clinical trials and mention them in introductory promotional materials. Such requirements are put forward only if the FDA is more concerned about the Side Effects Lawsuit Attorney of a drug. In October 2007, the FDA updated healthcare professionals about warnings related to prescription of Provigil, a lesser variant of Nuvigil.

In December 2010, the FDA rejected Cephalon’s request to allow Nuvigil pill to treat jet lag. Though there was no official word on the reason for not allowing the drug to treat jet lag, speculations were rife that the FDA had greater concerns on Side Effects Lawsuit Attorney of the drug. Similar circumstances had forced the pharmaceuticals major to abandon plans to market Nuvigil for schizophrenia treatment last June.

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Crestor Lawsuit Lipitor Side Effects


Setting a historic milestone in the U.S. pharmaceutical industry, a Washington federal judge has granted Ranbaxy exclusive rights to market generic Lipitor for six months. On May 2, the court dismissed Mylan's suit challenging the FDA decision to allow Ranbaxy exclusive rights to sell generic version of the drug. Ranbaxy has plans to introduce the drug with generic atorvastatin calcium in the United States on November 30. The new version will give users an option to buy Lipitor at a cheaper rate.

Sold by Pfizer, lipid-lowering medicine Lipitor is the top-selling prescription drug in the world. Lipitor lowers blood cholesterol, stabilizes plaque, and forbids strokes through anti-inflammatory mechanisms. It inhibits HMG-CoA reductase enzyme that helps in the production of cholesterol in humans. However, the drug can cause several side effects, including devastating effects on human muscle and nerve cells. Memory loss, fatigue, myopathy, insomnia, chest pain, urinary tract infection, myalgia, and severe allergic reaction are among the serious side effects of Lipitor.

A feature story entitled "Life After Lipitor" published by Californian newspaper Tahoe World on January 27, 2004 highlighted the plight of a Lipitor user from Tahoe City. Doug Peterson, the victim, developed severe neuromuscular problems within two years of taking Lipitor. He experienced lack of muscular coordination, loss of effective motor skills, balancing problems, and trouble talking. His health began improving after he stopped taking the drug. It followed by several reports in medical journals and websites highlighting numerous adverse side effects of the drug. Since then it has been linked to multiple sclerosis, memory loss, motor neuropathy, vertigo, disorientation, and stiffness in neck and calf muscles as corroborated by the users of the drug.

Lipitor Side Efects Class Action Lawsuit Attorney

A class action lawsuit was filed against Pfizer in June 2006 in New York State Supreme Court alleging failure to inform doctors and patients about serious side effects linked to Lipitor. It claimed that the drug caused memory loss and debilitating muscle and nerve problems to several users in New York and Atlanta. One of the plaintiffs, 60-year-old Atlanta man Charles M. Wilson, had complained that he continued suffering balancing problems, memory loss, and fatigue even three years after giving up Lipitor. Another lawsuit by 47-year-old New Yorker Michael Mazzariello alleged that he incurred debilitating damage to muscle cells and loss of memory after using cholesterol-lowering drugs, such as Lipitor. The complainants were of the view that Pfizer promoted the drug as safe and with minimal risks in its ads while doctors and patients came to know about its more dangerous side effects after using it.

Lipitor Side Effects Dangerous Lipitor

Atorvastatin, the main component in Lipitor, causes
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Vicodin Lawsuit Vicodin Side Effects Lawsuit Attorney

Vicodin Lawsuit Vicodin Side Effects Lawsuit AttorneyIn January 2011, the government announced its intention to limit use of some of the most popular prescription painkillers, including Vicodin. It cited reports of poisoning caused by many patients due to acetaminophen presence in these drugs. The FDA has granted three years to manufacturers of these narcotics drugs with acetaminophen to reformulate them. It has set a new limit of 325 milligrams of acetaminophen in Vicodin-like drugs, less than half of the amount presently allowed. Apart from these, manufacturers and distributors are required to have more explicit warning labels on these drugs.

Vicodin, which contains hydrocodone and paracetamol or acetaminophen mixture, is used to treat moderate to severe pain and cough. Doctors usually prescribe the drug for acute, chronic, or post-operative pains. Vicodin is effective in increasing the patient’s ability to deal with pain and speeds up the recovery process. However, it is listed under the U.S. Controlled Substances Act of 1970 for having hydrocodone, a semi-synthetic opioid analgesic. It has many side effects, including addiction blues.

Due to its widespread side effects, the U.S. laws control production, sale, and usage of Vicodin. Though doctors prescribe only controlled dosage to patients, users often experience dizziness, lightheadedness, vomiting, and sedation. The strength of the drug often induces many patients to become addicted to it. When abused, the drug is likely to influence physical and mental conditions of addicts.

Reports on Vicodin Side Effects

The FDA has named Vicodin a Schedule III drug with the warning that its misuse has the potential to cause

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Seroquel Side Effects Lawsuit Attorney


Seroquel Lawsuit AttorneyThe U.S. Agency for Healthcare Research Quality announced on May 24th its plan to conduct a nationwide survey on comparative impact of Seroquel and lithium on patients with bipolar disorder. It has earmarked $10 million to study the detailed impact of the drug on patients being treated at 10 hospitals in the country. This comes on the heels of a startling disclosure made by the Department of Health and Human Services in the first week of May about unauthorized administration of Seroquel and other strong antipsychotic drugs to elderly nursing home residents throughout the country. The report also alleged that such unnecessary administration thrived on the kickbacks paid by drug makers. The disclosure came after a Congressional member questioned about Seroquel second generation antipsychotic mood-stabilizing drug given to hundreds of thousands of elderly dementia patients staying in nursing homes.

AstraZeneca’s Seroquel, which contains Quetiapine, is an atypical antipsychotic drug used to treat schizophrenia, acute bipolar disorder, and severe depression. However, this second generation mood-stabilizing medication causes toxicity, serious neurological disorders, glucose intolerability, early onset of diabetes, and metabolic side effects in patients.

Seroquel Complaints

The FDA approved Seroquel in 1994 for treatment of schizophrenia. It was allowed as a medication for mania-associated bipolar disorder in 2004. However,

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Avandia Lawsuit Attorney

Avandia Side Effects Lawsuit

Avandia Diabetes Pill: Side Effects and Lawsuits

avandia lawsuit avandia side effectsThe FDA has announced a ban on the retail sale of diabetes drug Avandia with effect from November 18th. The decision of the federal regulator made public on May 17th was expected after several complaints of heart problems caused by the drug were surfaced in the recent years. Approved in 1999, Avandia is widely reported to have caused cardiovascular and other health problems in users. Various surveys and research reports have also linked the drug to increased heart attack risk in people with Type 2 diabetes.

Avandia, the generic name of the drug rosiglitazone, is already subject to restricted use in the United States following the FDA label changes in 2010 specifying minimum conditions required for users. The drug has caused more than 100,000 heart attacks in the United States and manufacturers GlaxoSmithKline (GSK) and SmithKline Beecham Corporation are facing several lawsuits for failing to inform users appropriately about its side effects.

Avandia Lawsuits

South Carolina State Sues Avandia Maker

Just a day before FDA decision on retail marketing ban, the
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