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Voydeya

Voydeya

Manufacturer:

Catalent CTS
Information is sourced from publicly available references. The information is for educational purpose of healthcare professionals and we are not liable for any loss or damage.
Core Prescribing Info
Contents
Danicopan
Indications/Uses
Add-on to ravulizumab or eculizumab for adult patients w/ paroxysmal nocturnal haemoglobinuria who have residual haemolytic anaemia.
Dosage/Direction for Use
Initially 150 mg tds, approx 8 hr apart (±2 hr). May increase to 200 mg tds after a min of 4 wk of treatment depending on clinical response. Severe renal impairment (eGFR <30 mL/min/1.73 m2) Initially 100 mg tds, approx 8 hr apart (±2 hr). May increase to 150 mg tds after a min of 4 wk of treatment depending on clinical response.
Administration
Should be taken with food.
Contraindications
Hypersensitivity. Patients w/ unresolved Neisseria meningitidis infection at treatment initiation. Patients who are not currently vaccinated against Neisseria meningitidis unless they receive prophylactic treatment w/ appropriate antibiotics until 2 wk after vaccination.
MIMS Class
Immunosuppressants
ATC Classification
L04AJ09 - danicopan ; Belongs to the class of complement inhibitors. Used as immunosuppressants.
Presentation/Packing
Form
Voydeya FC tab 100 mg
Packing/Price
1's
Form
Voydeya FC tab 50 mg
Packing/Price
1's
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