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Roche to discontinue Konakion Neonatal
Roche to discontinue Konakion Neonatal
Date published: 17/01/2006
The
Medicines and Healthcare products Regulatory Agency (MHRA) has announced that
Roche is to discontinue Konakion Neonatal. Konakion Neonatal is primarily used
to protect babies at birth with vitamin K deficiency and will be discontinued
on March 31st this year.
The product will be replaced by Konakion MM
Paediatric. The new treatment has previously been licensed to be given by
injection or by mouth to premature babies and those at special risk. MHRA has
also recently licensed it for intramuscular injection in healthy
babies.
With the introduction of the new way to administer Konakion MM
Paediatric health professionals are being advised that when given as an
intramuscular injection the volume of the injection is different to that they
are used to with the old product. MHRA has also licensed the use of Konakion MM
Paediatric to reverse the effects of anticoagulant therapy in babies and
infants, but under specialist advice.
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