Inhouse product
Indications
Secrin tablet is
indicated in following conditions-
* রেজিস্টার্ড চিকিৎসকের পরামর্শ মোতাবেক ঔষধ সেবন করুন'
Pharmacology
Glimepiride is a
sulfonylurea antidiabetic agent which decreases blood glucose concentration.
The primary mechanism of action of Glimepiride appears to be dependent on
stimulating the release of insulin from functioning pancreatic beta cells.
Glimepiride acts in concert with glucose by improving the sensitivity of beta
cells to physiological glucose stimulus, resulting in insulin secretion. In
addition, extrapancreatic effects like reduction of basal hepatic glucose
production, increased peripheral tissue sensitivity to insulin and glucose
uptake may also play role in the activity of Glimepiride. In non-fasting
diabetic patients, the hypoglycaemic action of a single dose of Glimepiride persists
for 24 hours.
Dosage
In principle, the
dosage of Glimepiride is governed by the desired blood sugar level. The dosage
of Glimepiride must be the lowest which is sufficient to achieve the desired
metabolic control. The initial and the maintenance doses are set based on the
results of regular check of glucose in blood and urine. Monitoring of glucose
levels in blood and urine also serves to detect either primary or secondary
failure of therapy.
Initial dose and dose
titration: the usual initial
dose is 1 mg once daily, if necessary, the daily dose can be increased. Any
increase can be based on regular blood sugar monitoring, and should be gradual,
i.e., at intervals of 1 to 2 weeks, and carried out stepwise, as follows: 1 mg
-> 2 mg -> 3 mg -> 4 mg -> 6 mg.
Dose in patients with
well controlled diabetes:
the usual dose range in patients with well controlled diabetes is 1 to 4 mg
daily.
Distribution of doses: Timing and distribution of doses are decided
by the physician, in consideration of the patient's current life-style.
Normally, a single daily dose is sufficient. This should be taken immediately
before a substantial breakfast or if none is taken immediately before the first
main meal. It is very important not to skip meals after taking the drug.
Secondary dosage
adjustment: As control of
diabetes improves, sensitivity to insuiin increases; therefore, Glimepiride
requirement may fall as treatment proceeds. To avoid hypoglycaemia, timely dose
reduction or cessation of Glimepiride therapy must be considered. A dose
adjustment must also be considered whenever the patient's weight or life-styie
changes, or other factors arise which cause an increased susceptibility to hypo
or hyperglycaemia.
Changeover from other
oral antidiabetics to Glimepiride: There is no exact dosage relationship between Glimepiride and
other oral blood sugar lowering agents. When substituting Glimepiride for other
such agents, the initial daily dose is 1 mg; this applies even in changeover
from maximum dose of other oral blood sugar lowering agents. Any dose increase
should be in accordance with guideline given above in 'initial dose and dose
titration'. Consideration must be given to the potency and duration of action
of the previous blood sugar lowering agent. It may be necessary to interrupt
treatment to avoid additive effects which would increase the risk of
hypoglycaemia.
* রেজিস্টার্ড চিকিৎসকের পরামর্শ মোতাবেক ঔষধ সেবন করুন'
Administration
Glimepiride tablet
must be swallowed with sufficient amount of liquid.
* রেজিস্টার্ড চিকিৎসকের পরামর্শ মোতাবেক ঔষধ সেবন করুন'
Interaction
Based on experience
with Secrin and known interactions for other sulfonylureas, the following
interactions must be considered.
In addition to insulin
and other oral antidiabetic agents, drugs which may potentiate the
hypoglycaemic action of Secrin include: ACE inhibitors, aminosalicylic acid, anabolic steroids and
male sex hormones, azapropazone, chloramphenicol, ciofibrate, coumarin
derivatives, cyclophosphamide, disopyramide, fenfluramine, fenyramidol,
fibrates, fluconazole, fluoxetine, guanethidine, ifosfamide, MAO-inhibitors,
miconazole, oxpentifylline (high dose parenteral), oxyphenbutazone,
para-aminosalicylic acid, phenylbutazone, probenecid, quinolones, salicylates,
sulphinpyrazone, sulfonamide antibiotics, tetracyclines, tritoqualine, trofosfamide.
Drugs which may attenuate the hypoglycaemic action of Secrin include:
Contraindications
Glimepiride is not
suitable for the treatment of insulin dependent (type I) diabetes mellitus, or
for the treatment of diabetic ketoacidosis, nor for the treatment of diabetic
coma. Glimepiride must not be used in patients hypersensitive to Glimepiride,
other sulfonylureas, other sulfonamides, severe hepatic dysfunction, severe
impairment of renal function and dialysis patients.
Side Effects
Hypoglycaemia,
temporary visual impairment, nausea, vomiting, diarrhoea, abdominal pain,
urticaria, fall in blood pressure.
Pregnancy &
Lactation
Glimepiride must not
be taken during pregnancy; a changeover to insulin is necessary. Patients
planning a pregnancy must inform their physician, and should change
over to insulin. Ingestion of Glimepiride with breast milk feeding may
harm the child. Therefore, Glimepiride must not be taken by breastfeeding
women. Either a changeover or complete discontinuation of breastfeeding is
necessary.
Precautions &
Warnings
in the initial weeks
of treatment, the risk of hypoglycaemia may be increased and necessitates
careful monitoring. If such risk present it may be necessary to adjust the
dosage of Secrin, Hypoglycaemia can almost be promptly controlled by immediate
intake of carbohydrates (glucose or sugar).
Overdose Effects
Overdosage of
sulfonylureas, including Secrin, can produce hypoglycaemia. Mild hypoglycaemic
symptoms without loss of consciousness or neurologic findings should be treated
aggressively with oral glucose and adjustments in drug dosage or meal patterns.
Close monitoring should continue until the physician is assured that the
patient is out of danger. Severe hypoglycaemic reactions with coma, seizure, or
other neurological impairment occur infrequently, but constitute medicai
emergencies requiring immediate hospitalization. If hypoglycaemic coma is
diagnosed or suspected, the patient should be given a rapid intravenous
injection of concentrated (50%) glucose solution. This should be followed
by a continuous infusion of a more dilute (10%) glucose solution at a rate that
will maintain the blood glucose at a level above 100 mg/dl. Patients should be
closely monitored for a minimum of 24 to 48 hours, because hypoglycaemia may
recur after apparent clinical recovery.
Therapeutic Class
Sulfonylureas
Storage Conditions
Do not store above
30°C. Keep away from light and out of the reach of children.
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