|RT | May 28, 2017|
The patient was reportedly treated with the drug Tysabri from Biogen for three years before receiving a single dose of the new drug Ocrevus by Roche in April. The subject later developed a rare brain infection called Progressive Multifocal Leukoencephalopathy (PML) which often results in “serious disability or death”.
Roche said it is investigating the cause of the infection with the patient’s previous diagnosis for John Cunningham virus being considered as a possible source.
The Swiss drugmaker acknowledged that, while there were no cases of PML recorded during its trials of Ocrevus, patients taking the drug were warned that there was a possible risk of developing a serious infection.
The risk is associated with all MS drugs that suppress the immune system. Dozens of patients undergoing treatment with Tysabri have been diagnosed with PML in the past, Reuters reports.
The US Food and Drug Administration (FDA) approved Tysabri for use in the country in March. This follows the regulator’s decision to take the drug off the market in 2005 after three patients involved in a clinical trial developed PML. Tsyabri was later reinstated with additional guidelines after users, for whom it was effective, demanded its return.
Roche claims the diagnosis was reported as a carry-over from Tysabri, otherwise known as natalizumab, by the patient’s physician. Tysabri manufacturer Biogen’s statement on the matter makes no mention of a possible connection to its drug.
"Biogen is aware that a patient taking Ocrevus has been diagnosed with PML, and we are currently assessing the information to confirm the reported PML," Biogen spokesman Matt Fearer told Reuters.
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