Very rare genetic disease Rx funded

June 29, 2016

INFANTS and children with a rare inherited genetic disease known as hereditary tyrosinaemia type 1 (HT-1) can now receive Orfadin (nitisinone from Menarini) under the Life Saving Drugs Program. With an incidence of only one or two babies each year diagnosed with the multiple organ failure disease, the drug offers new hope of infants living well past the normal five year standard. The special funding has been in effect since 01 Jun.

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Pharmacy Daily | Very rare genetic disease Rx funded

Very rare genetic disease Rx funded

Other recent headlines

LGP results set it for growth

On-site experts in aged care facilities

Pharmacist invention seeks US patent

SEARCH PHARMACY DAILY

Featured video

Recent issues

INDUSTRY JOB VACANCIES