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It was mentioned at the Haemophilia Reference Centre Directors meeting that the European (red) material was still available for those who felt it carried a lower risk of conveying hepatitis, although both were equally safe.

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In an internal memo, Dr Otto Schwarz managing director of Immuno AG stated that two types of Kryobulin would be sold. KRYOBULIN 1, made from European plasma and KRYOBULIN 2, made from US Licensed Source Plasma.

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A table published in June 1983 showed that Immuno Ltd's sales of Kryobulin (Red) exceeded sales of Kryobulin (Blue) by 4.5 times.

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In a memo from Mr Wrigglesworth to Mr Parker and others it was recorded that "Miles Labs state that FVIII manufactured from plasma collected since March 83' will not be available until August, and Immuno in September 83'".

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In her written witness statement to the Infected Blood Inquiry, Dr Diana Waford made reference to the Immuno's ethical obligation regarding American Kryobulin carrying a higher risk of hepatitis.

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In her written statement to the Infected Blood Inquiry, Dr Diana Walford elaborated on the translation of a German note regarding a "publication" showing that American Kryobulin had a higher hepatitis risk.

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It was stated regarding a Hepatitis Survey that all the cases of clinical hepatitis and almost all asymptomatic hepatitis were confined to patients restricted to commercial concentrates. No significant differences between Hemofil and Kryobulin.

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Speywood had a product licence to distribute Cutter's Koate, and by February 1980, Speywood later relabelled the Koate product and sold it as Humanate

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Speywood were informed that they could no longer sell relabelled Koate under the brand Humante as the CSM were unable to ensure the safety of the product.

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The last batch of Koate imported by Speywood was released by DHSS in February 1980.

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Dr Arthur Codd stated that it was known that viruses were transmitted in this way: "we knew there was always a risk there might be other things lurking there" adding that it had always been his advice to create a "pedigree herd" of volunteer donors in order to minimise the risk of infection. A decision was made to import commercial concentrates stating that "We could not have met demand at that time but we could have continued with the older products until Britain became self-sufficient."

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Professor Zuckerman told Michael Gillard that he had visited Immuno in Vienna, and thought it was a poor facility, which lacked medical back-up and had "dubious sources of plasma".

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The New England Journal of Medicine carried an article suggesting the recorded cases of the principal symptoms included in the syndrome might only represent the tip of the iceberg in terms of the prevalence of conditions associated with AIDS.

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It was reported to the World Congress of Blood Transfusion (Budapest) that is was suspected in the US that an infective agent in blood concentrates resulted in people with haemophilia dying of AIDS.

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Alpha confirmed that until further notice it would 'not be using the cryoprecipitated material from plasma from hepatitis B surface antibody donors in the manufacture of Antihemophilic Factor (Human).'

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Alpha confirmed that it had "voluntarily suspended until further notice the use of cryoprecipitated material from hepatitis B surface antibody donors in the manufacture of Antihemophilic Factor (Human)."

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Dr Denis Donohue of the FDA asked pharmaceutical companies to stop using blood collected from donors likely to have high levels of antibodies to Hepatitis.

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The Morbidity and Mortality Weekly report by the Centers for Disease Control reported 593 cases of AIDS, 243 of whom had died. It was reported that the CDC had been notified of 684 individuals who had been diagnosed with Kaposi's sarcoma and/or serious opportunistic infections resulting from an acquired immune deficiency and that at least 260 (41%) had died.

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By November 1982 the MMWR had reported 788 AIDS cases.

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It was reported that a baby in San Francisco had developed symptoms of AIDS after receiving transfusions. One of those transfusions had been given by a donor who was subsequently diagnosed with AIDS.

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