PREDNISOLONE- prednisolone syrup

Land: USA

Språk: engelsk

Kilde: NLM (National Library of Medicine)

Aktiv ingrediens:

PREDNISOLONE (UNII: 9PHQ9Y1OLM) (PREDNISOLONE - UNII:9PHQ9Y1OLM)

Tilgjengelig fra:

Preferred Pharmaceuticals Inc

Administreringsrute:

ORAL

Resept typen:

PRESCRIPTION DRUG

Indikasjoner:

Prednisolone Syrup (Prednisolone Oral Solution USP) is indicated in the following conditions: Primary or secondary adrenocortical insufficiency (hydrocortisone or cortisone is the first choice: synthetic analogs may be used in conjunction with mineralocorticoids where applicable; in infancy mineralocorticoid supplementation is of particular importance). Congenital adrenal hyperplasia Nonsuppurative thyroiditis Hypercalcemia associated with cancer As adjunctive therapy for short-term administration (to tide the patient over an acute episode or exacerbation) in: Psoriatic arthritis Rheumatoid arthritis, including juvenile rheumatoid arthritis (selected cases may require low-dose maintenance therapy) Ankylosing spondylitis Acute and subacute bursitis Acute nonspecific tenosynovitis Acute gouty arthritis Post-traumatic osteoarthritis Synovitis of osteoarthritis Epicondylitis During an exacerbation or as maintenance therapy in selected cases of: Systemic lupus erythematosus Acute rheumatic carditis Pemphigus Bullo

Produkt oppsummering:

Prednisolone Syrup (Prednisolone Oral Solution USP) is a cherry flavored red liquid containing 15 mg of prednisolone in each 5 mL (teaspoonful) and is supplied in 480 mL bottles NDC 68788-7207-4 Dispense with a suitable calibrated measuring device to assure proper measuring of dose.  15 mg prednisolone  = 1 teaspoon  10 mg prednisolone  = 2/3 teaspoon  7.5 mg prednisolone  = 1/2 teaspoon  5 mg prednisolone  = 1/3 teaspoon Dispense in tight, light-resistant and child-resistant containers as defined in the USP/NF. Store at 20° to 25°C (68° to 77°F) [see USP Controlled Room Temperature]. Do Not Refrigerate.

Autorisasjon status:

Abbreviated New Drug Application

Preparatomtale

PREDNISOLONE- PREDNISOLONE SYRUP
PREFERRED PHARMACEUTICALS INC
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PREDNISOLONE SYRUP
(PREDNISOLONE ORAL SOLUTION USP)
15 MG/5 ML
RX ONLY
DESCRIPTION
Prednisolone Syrup (Prednisolone Oral Solution USP) contains
prednisolone which is a glucocorticoid.
Glucocorticoids are adrenocortical steroids, both naturally occurring
and synthetic, which are readily
absorbed from the gastrointestinal tract.
Prednisolone is a white to practically white, odorless, crystalline
powder. It is very slightly soluble in
water; soluble in methanol and in dioxane; sparingly soluble in
acetone and in alcohol; slightly soluble
in chloroform.
The chemical name for prednisolone is
Pregna-1,4-diene-3,20-dione,11,17,21-trihydroxy-,(11β)-.
Prednisolone Syrup (Prednisolone Oral Solution USP) contains 15 mg of
prednisolone in each 5 mL.
Benzoic acid, 0.1% is added as a preservative. It also contains
alcohol 5% v/v, cherry flavor, citric
acid, edetate disodium, FD&C Blue #1, FD&C Red #40, glycerin,
propylene glycol, purified water,
sodium saccharin, and sucrose. Prednisolone Syrup (Prednisolone Oral
Solution USP) may contain
sodium citrate for pH adjustment.
CLINICAL PHARMACOLOGY
Naturally occurring glucocorticoids (hydrocortisone and cortisone),
which also have salt-retaining
properties, are used as replacement therapy in adrenocortical
deficiency states. Their synthetic analogs
such as prednisolone are primarily used for their potent
anti-inflammatory effects in disorders of many
organ systems.
Glucocorticoids such as prednisolone cause profound and varied
metabolic effects. In addition, they
modify the body's immune responses to diverse stimuli.
INDICATIONS AND USAGE
Prednisolone Syrup (Prednisolone Oral Solution USP) is indicated in
the following conditions:
Primary or secondary adrenocortical insufficiency (hydrocortisone or
cortisone is the first choice:
synthetic analogs may be used in conjunction with mineralocorticoids
where applicable; in infancy
mineralocorticoid supplementation is of particular importance).
Congenital adrenal h