ATAZANAVIR SULFATE capsule

Kraj: Stany Zjednoczone

Język: angielski

Źródło: NLM (National Library of Medicine)

Składnik aktywny:

ATAZANAVIR SULFATE (UNII: 4MT4VIE29P) (ATAZANAVIR - UNII:QZU4H47A3S)

Dostępny od:

REMEDYREPACK INC.

INN (International Nazwa):

ATAZANAVIR SULFATE

Skład:

ATAZANAVIR 300 mg

Droga podania:

ORAL

Typ recepty:

PRESCRIPTION DRUG

Wskazania:

Atazanavir sulfate capsules are indicated in combination with other antiretroviral agents for the treatment of HIV-1 infection for patients 6 years and older weighing at least 15 kg. Limitations of Use: - Atazanavir is not recommended for use in pediatric patients below the age of 3 months due to the risk of kernicterus. - Use of atazanavir/ritonavir in treatment-experienced patients should be guided by the number of baseline primary protease inhibitor resistance substitutions [see Microbiology ( 12.4)] . Atazanavir sulfate capsules are contraindicated: - in patients with previously demonstrated clinically significant hypersensitivity (e.g., Stevens-Johnson syndrome, erythema multiforme, or toxic skin eruptions) to any of the components of atazanavir sulfate capsules [see Warnings and Precautions ( 5.2)] . - when coadministered with drugs that are highly dependent on CYP3A or UGT1A1 for clearance, and for which

Podsumowanie produktu:

Atazanavir sulfate capsules are available as: 150 mg – capsules with light-turquoise-blue-opaque cap and aqua-blue-opaque body, imprinted “5526” on the body and “TEVA” on the cap, in bottles of 60 (NDC 0093-5526-06). 200 mg – capsules with light-turquoise body and light-turquoise cap, imprinted “93” over “5527” on both the cap and the body, in bottles of 60 (NDC 0093-5527-06). 300 mg – capsules with light-blue-opaque body and red-opaque cap, imprinted “93” over “5528” on both the cap and the body, in bottles of 30 (NDC 0093-5528-56). Dispense in a tight, light-resistant container as defined in the USP, with a child-resistant closure (as required). Store at 20° to 25°C (68° to 77°F) [See USP Controlled Room Temperature].

Status autoryzacji:

Abbreviated New Drug Application

Charakterystyka produktu

ATAZANAVIR SULFATE- ATAZANAVIR SULFATE CAPSULE
REMEDYREPACK INC.
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HIGHLIGHTS OF PRESCRIBING INFORMATION
THESE HIGHLIGHTS DO NOT INCLUDE ALL THE INFORMATION NEEDED TO USE
ATAZANAVIR SULFATE CAPSULES SAFELY
AND EFFECTIVELY. SEE FULL PRESCRIBING INFORMATION FOR ATAZANAVIR
SULFATE CAPSULES.
ATAZANAVIR SULFATE CAPSULES, FOR ORAL USE
INITIAL U.S. APPROVAL: 2003
RECENT MAJOR CHANGES
Dosage and Administration,
Testing Prior to Initiation and During Treatment with Atazanavir
Sulfate Capsules ( 2.2)
10/2017
Dosage of Atazanavir Sulfate Capsules in Pediatric Patients ( 2.4)
5/2017
Contraindications ( 4)
3/2018
Warnings and Precautions
Chronic Kidney Disease ( 5.5)
10/2017
INDICATIONS AND USAGE
Atazanavir sulfate capsules are a protease inhibitor indicated for use
in combination with other antiretroviral agents for the
treatment of HIV-1 infection for patients 6 years and older weighing
at least 15 kg. ( 1)
DOSAGE AND ADMINISTRATION
_Pretreatment testing:_ Renal laboratory testing should be performed
in all patients prior to initiation of atazanavir sulfate
capsules and continued during treatment with atazanavir sulfate
capsules. Hepatic testing should be performed in
patients with underlying liver disease prior to initiation of
atazanavir sulfate capsules and continued during treatment
with atazanavir sulfate capsules. ( 2.2)
_Treatment-naive adults:_ Atazanavir sulfate capsules 300 mg with
ritonavir 100 mg once daily with food or atazanavir 400
mg once daily with food. ( 2.3)
_Treatment-experienced adults:_ Atazanavir sulfate capsules 300 mg
with ritonavir 100 mg once daily with food. ( 2.3)
_Pediatric patients:_ Atazanavir sulfate capsule dosage is based on
body weight not to exceed the adult dose and must be
taken with food. ( 2.4)
_Pregnancy:_ Atazanavir sulfate capsules 300 mg with ritonavir 100 mg
once daily with food, with dosing modifications for
some concomitant medications. ( 2.6)
_Dosing modifications:_ may be required for concomitant therapy ( 2.3,
2.4, 2.6), renal impairment ( 2.7), and hepatic
impair