Progressive Multifocal Leukoencephalopathy, a life-threatening brain infection, has recently been linked to the use ofboth Rituxan and Raptiva.
What is Progressive Multifocal Leukoencephalopathy?
Progressive Multifocal Leukoencephalopathy (PML) is a serious, rare and fatal viral disease involving inflammation of the white matter of the brain. PML is caused by the JC virus (JCV). This virus is found in a lot of people, but usually does not cause symptoms. However, it triggers PML in people who have severe immune deficiency. PML is almost always deadly, and patients commonly die within 3-6 months of developing it.
Signs & Symptoms of Progressive Multifocal Leukoencephalopathy
The following is a list of signs and symptoms related to Progressive Multifocal Leukoencephalopathy:
- Mental deterioration
- Vision loss
- Speech disturbances
- Ataxia
- Paralysis
- Coma
- Seizures
- Muscle weakness
- Hemiparesis
- Facial weakness
- Dysphasia
- Memory failure
- Cognition failure
Progressive Multifocal Leukoencephalopathy Diagnosis and Treatment Options
PML is diagnosed by testing for the JC virus in cerebrospinal fluid or in a brain biopsy specimen. An MRI can also detect damage caused by PML in the brain. Other possible tests include Cytology exam of the urine, CT scan, or electroencephalography, a test to look at brain waves. Treatment consists of anti-viral and other medications including cidofovir and interleukin-2. Highly active antiretroviral therapy (HAART) is also a treatment used in some AIDS patients.
Do I Have a Progressive Multifocal Leukoencephalopathy Lawsuit?
The Schmidt Firm, LLP is currently accepting Rituxan and Raptiva induced Progressive Multifocal Leukoencephalopathy cases in all 50 states. If you or somebody you know has taken either Rituxan or Raptiva and since developed Progressive Multifocal Leukoencephalopathy, you should contact our firm immediately for a free case consultation. Please use the form below to contact our Dangerous Drug Litigation Group or call toll free 24 hours a day at (866) 920-0753.
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