DONEPEZIL HYDROCHLORIDE- donepezil hydrochloride tablet, film coated

Riik: Ameerika Ühendriigid

keel: inglise

Allikas: NLM (National Library of Medicine)

Toimeaine:

DONEPEZIL HYDROCHLORIDE (UNII: 3O2T2PJ89D) (DONEPEZIL - UNII:8SSC91326P)

Saadav alates:

KAISER FOUNDATION HOSPITALS

INN (Rahvusvaheline Nimetus):

Donepezil Hydrochloride

Koostis:

Donepezil Hydrochloride 10 mg

Manustamisviis:

ORAL

Retsepti tüüp:

PRESCRIPTION DRUG

Näidustused:

Donepezil hydrochloride tablets, USP are indicated for the treatment of dementia of the Alzheimer's type. Efficacy has been demonstrated in patients with mild, moderate, and severe Alzheimer's disease. Donepezil hydrochloride tablets are contraindicated in patients with known hypersensitivity to donepezil hydrochloride or to piperidine derivatives. Pregnancy Category C  There are no adequate or well-controlled studies in pregnant women. Donepezil hydrochloride should be used during pregnancy only if the potential benefit justifies the potential risk to the fetus. Oral administration of donepezil to pregnant rats and rabbits during the period of organogenesis did not produce any teratogenic effects at doses up to 16 mg/kg/day (approximately 6 times the maximum recommended human dose [MRHD] of 23 mg/day on a mg/m 2 basis) and 10 mg/kg/day (approximately 7 times the MRHD on a mg/m 2 basis), respectively. Oral administration of donepezil (1, 3, 10 mg/kg/day) to rats during late gestation and throughout lac

Toote kokkuvõte:

Supplied as white to off-white, round, film-coated tablets containing either 5 mg or 10 mg of donepezil hydrochloride, USP. The 5 mg tablets are white to off-white, round, film-coated tablets, debossed with “J” on one side and “5” on the other side. The 10 mg tablets are white to off-white, round, film-coated tablets, debossed with “J” on one side and “10” on the other side. Bottles of 2160                                       NDC 0179-0208-88 Storage: Store at 20°C-25°C (68°F-77°F), excursions permitted to 15°C-30°C (59°F-86°F). [See USP Controlled Room Temperature].

Volitamisolek:

Abbreviated New Drug Application

Toote omadused

DONEPEZIL HYDROCHLORIDE- DONEPEZIL HYDROCHLORIDE TABLET, FILM COATED
KAISER FOUNDATION HOSPITALS
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HIGHLIGHTS OF PRESCRIBING INFORMATION
THESE HIGHLIGHTS DO NOT INCLUDE ALL THE INFORMATION NEEDED TO USE
DONEPEZIL HYDROCHLORIDE TABLETS, USP SAFELY
AND EFFECTIVELY. SEE FULL PRESCRIBING INFORMATION FOR DONEPEZIL
HYDROCHLORIDE TABLETS, USP.
DONEPEZIL HYDROCHLORIDE TABLETS, USP FOR ORAL USE
INITIAL U.S. APPROVAL: 1996
INDICATIONS AND USAGE
Donepezil is a acetycholinesterase inhibitor indicated for the
treatment of dementia of the Alzheimer's type. Efficacy has
been demonstrated in patients with mild, moderate, and severe
Alzheimer's Disease ( 1).
DOSAGE AND ADMINISTRATION
Mild to Moderate Alzheimer’s Disease: 5 mg to 10 mg once daily (
2.1)
Moderate to Severe Alzheimer’s Disease:10 mg to 23 mg once daily
(2.2)
DOSAGE FORMS AND STRENGTHS
● Tablets: 5 mg and 10 mg ( 3)
CONTRAINDICATIONS
● Known hypersensitivity to donepezil hydrochloride or to piperidine
derivatives (4) (4)
WARNINGS AND PRECAUTIONS
Cholinesterase inhibitors are likely to exaggerate
succinylcholine-type muscle relaxation during anesthesia ( 5.1)
Cholinesterase inhibitors may have vagotonic effects on the sinoatrial
and atrioventricular nodes manifesting as
bradycardia or heart block ( 5.2)
Donepezil hydrochloride can cause vomiting. Patients should be
observed closely at initiation of treatment and after
dose increases ( 5.3)
Patients should be monitored closely for symptoms of active or occult
gastrointestinal (GI) bleeding, especially those at
increased risk for developing ulcers ( 5.4)
The use of donepezil hydrochloride in a dose of 23 mg once daily is
associated with weight loss ( 5.5)
Cholinomimetics may cause bladder outflow obstructions ( 5.6)
Cholinomimetics are believed to have some potential to cause
generalized convulsions ( 5.7)
Cholinesterase inhibitors should be prescribed with care to patients
with a history of asthma or obstructive pulmonary
disease ( 5.8)
ADVERSE REACTIONS
Most common adverse reactions in clinical studie