CALCIUM ACETATE capsule

Ország: Egyesült Államok

Nyelv: angol

Forrás: NLM (National Library of Medicine)

Aktív összetevők:

CALCIUM ACETATE (UNII: Y882YXF34X) (CALCIUM CATION - UNII:2M83C4R6ZB)

Beszerezhető a:

Atlantic Biologicals Corps

INN (nemzetközi neve):

CALCIUM ACETATE

Összetétel:

CALCIUM ACETATE 667 mg

Az alkalmazás módja:

ORAL

Recept típusa:

PRESCRIPTION DRUG

Terápiás javallatok:

Calcium acetate is a phosphate binder indicated to reduce serum phosphorus in patients with end stage renal disease (ESRD). Patients with hypercalcemia. Pregnancy Category C Calcium acetate capsules contain calcium acetate. Animal reproduction studies have not been conducted with calcium acetate, and there are no adequate and well controlled studies of calcium acetate use in pregnant women. Patients with end stage renal disease may develop hypercalcemia with calcium acetate treatment [see ]. Maintenance of normal serum calcium levels is important for maternal and fetal well being. Hypercalcemia during pregnancy may increase the risk for maternal and neonatal complications such as stillbirth, preterm delivery, and neonatal hypocalcemia and hypoparathyroidism. Calcium acetate treatment, as recommended, is not expected to harm a fetus if maternal calcium levels are properly monitored during and following treatment. Warnings and Precautions (5.1) The effects of calcium acetate

Termék összefoglaló:

NDC:17856-0377-2 in a CASE of 50 CAPSULES

Engedélyezési státusz:

Abbreviated New Drug Application

Termékjellemzők

CALCIUM ACETATE- CALCIUM ACETATE CAPSULE
ATLANTIC BIOLOGICALS CORPS
----------
HIGHLIGHTS OF PRESCRIBING INFORMATION
THESE HIGHLIGHTS DO NOT INCLUDE ALL THE INFORMATION NEEDED TO USE
CALCIUM ACETATE CAPSULES SAFELY AND
EFFECTIVELY. SEE FULL PRESCRIBING INFORMATION FOR CALCIUM ACETATE
CAPSULES. CALCIUM ACETATE CAPSULES, 667 MG
INITIAL U.S. APPROVAL: 1990
INDICATIONS AND USAGE
• Calcium acetate is a phosphate binder indicated for the reduction
of serum phosphorus in patients with end stage renal
disease. (1)
DOSAGE AND ADMINISTRATION
• Starting dose is 2 capsules with each meal. (2)
• Titrate the dose every 2-3 weeks until acceptable serum phosphorus
level is reached. Most patients require 3-4 capsules
with each meal. (2)
DOSAGE FORMS AND STRENGTHS
• Capsule: 667 mg calcium acetate capsules. (3)
CONTRAINDICATIONS
• Hypercalcemia. (4)
WARNINGS AND PRECAUTIONS
Treat mild hypercalcemia by reducing or interrupting calcium acetate
capsules and Vitamin D. Severe hypercalcemia
may require hemodialysis and discontinuation of calcium acetate
capsules. ( ) 5.1
Hypercalcemia may aggravate digitalis toxicity. ( ) 5.2
ADVERSE REACTIONS
The most common (> 10%) adverse reactions are hypercalcemia, nausea
and vomiting. ( ) 6.1
In clinical studies, patients have occasionally experienced nausea
during calcium acetate therapy. ( ) 6
TO REPORT SUSPECTED ADVERSE REACTIONS, CONTACT CAMBER PHARMACEUTICALS
INC. AT 1-866-495-8330 OR
FDA AT 1-800-FDA-1088 OR WWW.FDA.GOV/MEDWATCH.
DRUG INTERACTIONS
Calcium acetate may decrease the bioavailability of tetracyclines or
fluoroquinolones. ( ) 7
When clinically significant drug interactions are expected, administer
the drug at least one hour before or at least three
hours after calcium acetate or consider monitoring blood levels of the
drug. ( ) 7
SEE 17 FOR PATIENT COUNSELING INFORMATION.
REVISED: 5/2016
FULL PRESCRIBING INFORMATION: CONTENTS*
1 INDICATIONS AND USAGE
2 DOSAGE AND ADMINISTRATION
3 DOSAGE FORMS AND STRENGTHS
4 CONTRAINDICATIONS
5 WARNINGS AND PRECAUTIONS
5.2 Concomitant U