Inhouse product
Indications
Endocrine Disorders: Primary or Secondary Adrenocortical
Insufficiency, Congenital Adrenal Hyperplasia, Nonsuppurative Thyroiditis,
Hypercalcemia associated with Cancer.
Rheumatic Disorders: Juvenile Rheumatoid Arthritis, Ankylosing
Spondylitis, Acute and Subacute Bursitis, Synovitis of Osteoarthritis, Acute
nonspecific Tenosynovitis, Post-traumatic Osteoarthritis, Psoriatic Arthritis,
Epicondylitis, Acute Gouty Arthritis.
Collagen Diseases: Systemic lupus Erythematosus, Systemic
Dermatomyositis and Acute Rheumatic Carditis.
Dermatologic Diseases: Bullous Dermatitis Herpetiformis, Severe
Erythema Multiforme (Stevens-Johnson syndrome), Severe Seborrheic Dermatitis,
Exfoliative Dermatitis, Mycosis Fungoides, Pemphigus, Severe Psoriasis.
Allergy: Seasonal or Perennial Allergic Rhinitis,
Drug hypersensitivity reactions, Serum Sickness, Contact Dermatitis, Bronchial
Asthma and Atopic Dermatitis;
Ophthalmic Diseases: Allergic Corneal Ulcers, Herpes Zoster
Ophthalmicus, Anterior segment inflammation, Sympathetic Ophthalmia, Keratitis,
Optic Neuritis, Allergic Conjunctivitis, Chorioretinitis, iritis end
iridocyclitis.
Respiratory Diseases: Symptomatic sarcoidosis, Loeffler's syndrome
not manageable by other means, berylliosis, Aspiration Pneumonitis.
Hematological
Disorders: Idiopathic
Thrombocytopenic Purpura in adults, Secondary Thrombocytopenia in adults,
Acquired (Autoimmune) Hemolytic Anemia, Erythroblastopenia, 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
Disease: To tide the patient
over a critical period of the disease in Ulcerative Colitis & Regional
Enteritis.
CNS Disease: Acute Exacerbations of Multiple Sclerosis.
* রেজিস্টার্ড চিকিৎসকের পরামর্শ মোতাবেক ঔষধ সেবন করুন'
Description
Methipred is a potent
anti-inflammatory steroid. It has greater anti-inflammatory potency than
Prednisolone, even less tendency than prednisolone to induce sodium and water
retention. The relative potency of Methipred to Hydrocortisone is at least four
to one.
Pharmacology
Pharmacodynamic
properties: Methylprednisolone
Is a potent anti-inflammatory agent with the capacity to profoundly inhibit the
immune system. Glucocorticoids primarily bind to and activate intracellular
glucocorticoid receptors that being activated bind to promoter regions of DMA
(which may activate or suppress transcription) and activate transcription
factors that result in inactivation of genes through deacetylation of histones.
Methylprednisolone influences the kidney and fluid & electrolyte balance,
lipid,
protein, and carbohydrate metabolism, skeletal muscle, the cardiovascular
system, the immune system, the nervous system, and the endocrine system.
Pharmacokinetic
properties: The absolute
bioavailability of Methylprednisclone is generally high (82% to 89%) following
oral administration and rapidly absorbed and the maximum plasma concentration
is achieved around 1.5 to 2.3 hours across doses following oral administration
in normal healthy adults. Methylprednisolone is widely distributed into the
tissues and its volume of distribution is 41-61.5 liter. It crosses the
Wood-brain barrier and the placental barrier and is secreted in breast milk.
The plasma protein binding of Methylprednisolone in humans is approximately
77%. Methylprednisolone is metabolized in the liver to inactive metabolites. No
dosing adjustments are necessary for renal failure. Methylprednisolone is
haemodializable.
Dosage &
Administration
The usual range is
2-48 mg daily in divided doses, depending on the specific disease being
treated.
As anti-inflammatory
or immunosuppressive initial dosage: As anti-inflammatory or immunosuppressive, the initial dosage
of Methylprednisolone tablets may vary from 4-48 mg per day depending on the
specific disease entity being treated, in situations of less severity lower
doses will generally suffice while in selected patients higher initial doses
may be required. The initial dosage should be maintained or adjusted until a
satisfactory response is noted. If after a reasonable period of time there is a
lack of satisfactory dirtied response, Methylprednisolone should be
discontinued and the patient transferred to other appropriate therapy. 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.
As anti-inflammatory
or immunosuppressive maintenance dosage: After a favorable response is noted, the proper maintenance
dosage should be determined by decreasing the initial drug dosage in small
decrements at appropriate time intervals until the lowest dosage which will
maintain an adequate clinical response is reached. It should be kept in mind
that constant monitoring is needed in regard to drug dosage. If after long-term
therapy the drug is to be stopped, it is recommended that it be withdrawn
gradually rather than abruptly.
Multiple Sclerosis: In the treatment of acute exacerbations of
multiple sclerosis, daily doses of 160 mg of Methylprednisolone for a week
followed by 64 mg every other day for 1 month have been shown to be effective.
Methylprednisolone 4 mg tablet can be used to treat and to control severe
allergy end dermatitis following the guideline listed below to minimize the
steroid withdrawal syndromes:
Alternate-day
therapy (ADT): Alternate-day
therapy is a corticosteroid dosing regimen in which twice the usual daily dose
of corticoid is administered every other morning. The purpose of this mode of
therapy is to provide the patient requiring long-term pharmacologic dose
treatment with the beneficial effects of corticoids, white minimizing certain
undesirable effects, including pituitary-adrenal suppression, Cushingoid stats,
Corficoid withdrawal symptoms, and growth suppression in children.
The following should be kept in mind when considering alternate-day therapy:
* রেজিস্টার্ড চিকিৎসকের পরামর্শ মোতাবেক ঔষধ সেবন করুন'
Interaction
Erythromycin,
Clarithromycin, Phenobarbital, Phenytoin, Rifampin and Ketoconazole inhibit the
metabolism of Methipred. Estrogens, including With control pills, can increase
the effect of corticosteroids by 50%. Cyclosporin reduces the metabolism of
Methipred. while Methipred reduces the metabolism of Cyclosporin. Methipred may
increase or decrease the effect of blood thinners (e.g. Warfarin). For all
these Interactions, the dose of Methipred may need to be lowered.
Contraindications
Systemic fungal
infections arid known hypersensitivity to components.
Side Effects
Short courses of
Methipred are usually well-tolerated with few, mild side effects. Long term,
high doses of Methyiprednisoione may produce predictable and potentially
serious side effects. Whenever possible, the lowest effective doses of
Methipred should be used for the shortest length of time to minimize side
effects. Alternate day dosing also can help reduce side effects. Side effects
of Methipred and other corticosteroids range from mild annoyances to serious
irreversible bodily damage. Side effects include fluid retention, weight gain,
high blood pressure, potassium loss, headache, muscle weakness, hair growth on
the face, glaucoma, cataracts, peptic ulceration, growth retardation in
children, convulsions, and psychic disturbances including depression, euphoria,
insomnia etc. Prolonged use of Methipred can depress the ability of the body's
adrenal glands to produce corticosteroids. Abruptly stopping Methipred in these
individuals can cause symptoms of corticosteroid insufficiency, with
accompanying nausea, vomiting, and even shock. Therefore, withdrawal of
Methipred usually is accomplished by gradually lowering the dose. Gradually
tapering Methipred not only minimizes the symptoms of corticosteroid
insufficiency, it also reduces the risk of an abrupt flare of the disease being
treated.
Pregnancy &
Lactation
Pregnancy category C.
Dregs should be given only if the potential benefit justifies the potential
risk te the foetus. Mefhyiprednisofone has not been adequately evaluated in
nursing mothers.
Precautions &
Warnings
Adrenocortical
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 secretion may be
impaired, salt and/or a mineralocorticoid should be administered concurrently.
There is an enhanced effect of corticosteroids on patients with hypothyroidism
and in those with cirrhosis. Corticosteroids should be used cautiously in
patients with ocular herpes simplex because of possible corneal perforation.
Aspirin should be used cautiously in conjunction with corticosteroids in
hypoprothrombinemia. The growth and development of infants and children on
prolonged corticosteroid therapy should be carefully observed.
Overdose Effects
Report of acute
toxicity and/or death following an overdose of glucocorticoid ere rare. No
specific antidote is available; treatment is supportive and symptomatic. Serum
electrolytes should be monitored.
Therapeutic Class
Glucocorticoids
Storage Conditions
Store in a cool and
dry place, away from light. Keep out of reach of children.
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