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Prednisone

REMEDYREPACK INC.


FULL PRESCRIBING INFORMATION: CONTENTS*




FULL PRESCRIBING INFORMATION

PREDNISONE DESCRIPTION


Prednisone



1 mg:anhydrous lactose, corn starch, lactose monohydrate, magnesium stearate, microcrystalline cellulose, sodium starch glycolate.|
2.5 mg:anhydrous lactose, colloidal silicon dioxide, magnesium stearate, microcrystalline cellulose, sodium starch glycolate, and talc.
5 mg:anhydrous lactose, colloidal silicon dioxide, magnesium stearate, microcrystalline cellulose, sodium starch glycolate, and talc.
10 mg:anhydrous lactose, colloidal silicon dioxide, magnesium stearate, microcrystalline cellulose, sodium starch glycolate, and talc.
20 mg:anhydrous lactose, D&C Yellow No. 10 Aluminum Lake, FD&C Yellow No. 6 Aluminum Lake, magnesium stearate, microcrystalline cellulose, and sodium starch glycolate.

CLINICAL PHARMACOLOGY



INDICATIONS & USAGE


     Endocrine disorders
     
Primary or secondary adrenocortical insufficiency (hydrocortisone or cortisone is the first choice; snythetic 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
     Rheumatic disorders
     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
     Collagen diseases
     During an exacerbation or as maintenance therapy in selected cases of:     
Systemic lupus erythematosus     
Systemic dermatomyositis (polymyositis)     
Acute rheumatic carditis
     Dermatologic diseases
     Pemphigus     
Bullous dermatitis herpetiformis     
Severe erythema multiforme (Stevens-Johnson syndrome)     
Exfoliative dermatitis     
Mycosis fungoides     
Severe psoriasis     
Severe seborrheic dermatitis
     Allergic states
     Control of severe or incapacitating allergic conditions intractable to adequate trials of conventional treatment:     
Seasonal or perennial allergic rhinitis     
Serum sickness     
Bronchial asthma     
Contact dermatitis     
Atopic dermatitis     
Drug hypersensitivity reactions
     Ophthalmic diseases
     Severe acute and chronic allergic and inflammatory processes involving the eye and its adnexa such as:     
Allergic conjunctivitis     
Keratitis     
Allergic corneal marginal ulcers     
Herpes zoster ophthalmicus     
Iritis and iridocyclitis     
Chorioretinitis     
Anterior segment inflammation     
Diffuse posterior uveitis and choroiditis     
Optic neuritis     
Sympathetic ophthalmia
     Respiratory diseases
     Symptomatic sarcoidosis     
Loeffler's syndrome not manageable by other means     
Berylliosis     
Fulminating or disseminated pulmonary tuberculosis when used concurrently with appropriate antituberculous chemotherapy     
Aspiration pneumonitis
     Hematologic disorders
     Idiopathic thrombocytopenic purpura in adults     
Secondary thrombocytopenia in adults     
Acquired (autoimmune) hemolytic anemia     
Erythroblastopenia (RBC anemia)     
Congenital (erythroid) hypoplastic anemia
     Neoplastic diseases
     For palliative management of:     
Leukemias and lymphomas in adults     
Acute leukemia of childhood
     Edematous states
     To induce a diuresis or remission of proteinuria in the nephrotic syndrome, without uremia, of the idiopathic type or that due to lupus erythematosus
     Gastrointestinal diseases
     To tide the patient over a critical period of the disease in:     
Ulcerative colitis     
Regional enteritis
     Nervous System
     Acute exacerbations of multiple sclerosis
     Miscellaneous
     Tuberculous meningitis with subarachnoid block or impending block when used concurrently with appropriate antituberculous chemotherapy     
Trichinosis with neurologic or myocardial involvement

PREDNISONE CONTRAINDICATIONS


WARNINGS





Usage in Pregnancy


While on corticosteroid therapy patients should not be vaccinated against smallpox. Other immunization procedures should not be undertaken in patients who are on corticosteroids, especially on high dose, because of possible hazards of neurological complications and a lack of antibody response.



PRECAUTIONS

General
Drug-induced adrenocortical insufficiency may be minimized by gradual reduction of dosage. This types of relative insufficiency may persist for months after discontinuation of therapy; therefore, in any situation of stress occurring during that period, hormone therapy should be reinstituted. Since mineralocorticoid secreation may be impaired, salt and/or a mineralocorticoid should be administered concurrently.








DOSAGE AND ADMINISTRATION.)


PREDNISONE ADVERSE REACTIONS

Fluid and Electrolyte Disturbances:
Sodium retention
Fluid retention
Congestive heart failure in susceptible patients
Potassium loss
Hypokalemic alkalosis
Hypertension
Musculoskeletal:
Muscle weakness
Steroid myopathy
Loss of muscle mass
Osteoporosis
Vertebral compression fractures
Aseptic necrosis of femoral and humeral heads
Pathologic fracture of long bones
Gastrointestinal:
Peptic ulcer with possible perforation and hemorrhage
Pancreatitis
Abdominal distention
Ulcerative esophagitis
Dermatologic:
Impaired wound healing
Thin fragile skin
Petechiae and ecchymoses
Facial erythema
Increased sweating
May suppress reactions to skin tests
Neurological:
Convulsions
Increased intracranial pressure with papilledema (pseudotumor cerebri) usually after treatment
Vertigo
Headache
Endocrine:
Menstrual irregularities
Development of Cushingoid state
Suppression of growth in children
Secondary adrenocortical and pituitary unresponsiveness, particularly in times of stress, as in trauma, surgery or illness
Decreased carbohydrate tolerance
Manifestations of latent diabetes mellitus
Increased requirements for insulin or oral hypoglycemic agents in diabetics
Ophthalmic:
Posterior subcapsular cataracts
Increased intraocular pressure
Glaucoma
Exophthalmos
Metabolic:
Negative nitrogen balance due to protein
Additional Reactions:
Urticaria and other allergic, anaphylactic or hypersensitivity reactions
www.fda.gov/medwatch.

DOSAGE & ADMINISTRATION


IT SHOULD BE EMPHASIZED THAT DOSAGE REQUIREMENTS ARE VARIABLE AND MUST BE INDIVIDUALIZED ON THE BASIS OF THE DISEASE UNDER TREATMENT AND THE RESPONSE OF THE PATIENT.


Multiple Sclerosis


ADT(Alternate Day Therapy)















HOW SUPPLIED






















STORAGE AND HANDLING



REFERENCES



PACKAGE LABEL.PRINCIPAL DISPLAY PANEL SECTION














Prednisone


Prednisone

Prednisone

PREDNISONE TABLET

Product Information

Product Type Human prescription drug label Item Code (Source) NDC:49349-997(NDC:0143-1477)
Route of Administration ORAL DEA Schedule

Active Ingredient/Active Moiety

Ingredient Name Basis of Strength Strength
PREDNISONE PREDNISONE 20 mg

Inactive Ingredients

Ingredient Name Strength
ANHYDROUS LACTOSE
D&C YELLOW NO. 10
FD&C YELLOW NO. 6
MAGNESIUM STEARATE
cellulose, microcrystalline
SODIUM STARCH GLYCOLATE TYPE A POTATO

Product Characteristics

Color Size Imprint Code Shape
red 9 mm Westward;477 ROUND

Packaging

# Item Code Package Description Marketing Start Date Marketing End Date
1 NDC:49349-997-02 30 in 1 BLISTER PACK

Marketing Information

Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
ANDA ANDA083677 2012-09-13


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