Regulatory Information
PFIZER PRIVATE LIMITED
PFIZER PRIVATE LIMITED
Therapeutic
Prescription Only
Formulation Information
CAPSULE
**4.2 Posology and method of administration** Posology The recommended dose of VYNDAQEL/VYNDAMAX is 61 mg tafamidis orally once daily (see Section 5.1 – _please refer to the Product Insert/Patient Information Leaflet published on HSA for the full drug information_) or 80 mg tafamidis meglumine (administered as four 20 mg capsules) once daily. VYNDAQEL/VYNDAMAX can be taken with or without food. A single 61 mg tafamidis capsule is bioequivalent to 80 mg tafamidis meglumine (four 20 mg tafamidis meglumine capsules). The two formulations are not interchangeable on a per mg basis (see Sections 5.1 and 5.2 – _please refer to the Product Insert/Patient Information Leaflet published on HSA for the full drug information_). Special populations _Paediatric_ VYNDAQEL/VYNDAMAX should not be prescribed in the paediatric population as transthyretin amyloidosis is not a disease present in this population. _Elderly_ No dosage adjustment is required for elderly patients (≥65 years) (see Section 5.2 – _please refer to the Product Insert/Patient Information Leaflet published on HSA for the full drug information_). _Renal or hepatic impairment_ No dosage adjustment is required for patients with renal impairment, or mild or moderate hepatic impairment. VYNDAQEL/VYNDAMAX has not been studied in patients with severe hepatic impairment. Method of administration Oral use. The capsule(s) should be swallowed whole and not crushed or cut. VYNDAQEL/VYNDAMAX may be taken with or without food. If a dose is missed, the patient should take the dose as soon as remembered. If it is almost time for the next dose, the patient should skip the missed dose and take the next dose at the regularly scheduled time. Do not double the dose.
ORAL
Medical Information
**4.1 Therapeutic indications** VYNDAQEL/VYNDAMAX is indicated for the treatment of transthyretin amyloidosis in adult patients with wild-type or hereditary cardiomyopathy to reduce all-cause mortality and cardiovascular-related hospitalisation.
**4.3 Contraindications** Hypersensitivity to the active substance or to any of the excipients of VYNDAQEL/VYNDAMAX (see Section 6.1 – _please refer to the Product Insert/Patient Information Leaflet published on HSA for the full drug information_).
N07XX08
tafamidis
Manufacturer Information
PFIZER PRIVATE LIMITED
Catalent Pharma Solutions
AndersonBrecon Inc. (Primary packager)
Active Ingredients
Documents
Package Inserts
Vyndaqel Soft Gelatin Capsule PI.pdf
Approved: June 28, 2023