Inhouse product
Indications
Linaptin M is
indicated as an adjunct to diet and exercise to improve glycemic control in
adults with type 2 diabetes mellitus when treatment with both Linagliptin and
Metformin Hydrochloride is appropriate
* রেজিস্টার্ড চিকিৎসকের পরামর্শ মোতাবেক ঔষধ সেবন করুন'
Pharmacology
Linagliptin is
indicated to improve glycemic control in patients with type 2 diabetes
mellitus. Linagliptin is an inhibitor of DPP-4 (dipeptidyl peptidase-4), an
enzyme that degrades the incretin hormones GLP-1 (glucagon like peptide-1) and
GIP (glucose dependent insulinotropic polypeptide). Thus, Linagliptin increases
the concentrations of active incretin hormones, stimulating the release of
insulin from pancreatic beta (β) cells in a glucose-dependent manner and
decreasing the secretion of glucagon from pancreatic alpha (α) cells in the
circulation.
Metformin Hydrochloride is a biguanide type oral antihyperglycemic drug used in
the management of type 2 diabetes. It lowers both basal and postprandial plasma
glucose. Its mechanism of action is different from those of sulfonylureas and
it does not produce hypoglycemia. Metformin Hydrochloride decreases hepatic
glucose production, decreases intestinal absorption of glucose and improves
insulin sensitivity by an increase in peripheral glucose uptake and utilization.
Dosage &
Administration
Linagliptin &
Metformin immediate release tablet: The dosage of Linagliptin & Metformin should be
individualized on the basis of both effectiveness and tolerability. Maximum
recommended dose of 2.5 mg Linagliptin and 1000 mg Metformin Hydrochloride
twice daily with meals. Dose escalation should be gradual to reduce the
gastrointestinal (GI) side effects associated with Metformin Hydrochloride use.
Recommended starting dose: In patients currently not treated with Metformin
Hydrochloride, initiate treatment with 2.5 mg Linagliptin and 500 mg Metformin
Hydrochloride twice daily.
In patients already treated with Metformin Hydrochloride, start with 2.5 mg
Linagliptin and the current dose of Metformin Hydrochloride twice daily.
Patients already treated with Linagliptin and Metformin Hydrochloride,
individual components may be switched to this combination containing the same
doses of each component.
Linagliptin &
Metformin extend release tablet: The dosage of this combination should be individualized on the
basis of both effectiveness and tolerability, while not exceeding the maximum
recommended total daily dose of Linagliptin 5 mg and Metformin Hydrochloride
2000 mg. this combination should be given once daily with a meal.
Recommended starting dose: In patients currently not treated with metformin,
initiate this combination treatment with 5 mg Linagliptin/1000 mg Metformin
Hydrochloride extended-release once daily with a meal.
In patients already treated with Metformin, start this combination with 5 mg of
Linagliptin total daily dose and a similar total daily dose of Metformin once
daily with a meal.
In patients already treated with Linagliptin & Metformin immediate release
tablet, switch to extend release tablet containing 5 mg of Linagliptin total
daily dose and a similar total daily dose of Metformin once daily with a meal.
5 mg Linagliptin & 1000 mg Metformin Hydrochloride extended-release tablet
should be taken as a single tablet once daily. Patients using 2.5 mg
Linagliptin & 1000 mg Metformin extended release tablets should take two
tablets together once daily.
* রেজিস্টার্ড চিকিৎসকের পরামর্শ মোতাবেক ঔষধ সেবন করুন'
Interaction
Cationic Drugs: Cationic drugs (e.g., amiloride, digoxin,
morphine, procainamide, quinidine, quinine, ranitidine, triamterene,
trimethoprim, or vancomycin) that are eliminated by renal tubular secretion
theoretically have the potential for interaction with Metformin by competing
for common renal tubular transport systems. Although such interactions remain
theoretical (except for cimetidine), careful patient monitoring and dose
adjustment of Linaptin M and/or the interfering drug is recommended in patients
who are taking cationic medications that are excreted via the proximal renal
tubular secretory system.
Carbonic Anhydrase
Inhibitors: Topiramate or other
carbonic anhydrase inhibitors (e.g., zonisamide, acetazolamide or
dichlorphenamide) frequently decrease serum bicarbonate and induce non-anion
gap, hyperchloremic metabolic acidosis. Concomitant use of these drugs may
induce metabolic acidosis. Use these drugs with caution in patients treated
with Linaptin M, as the risk of lactic acidosis may increase.
Inducers of
P-glycoprotein and CYP3A4 Enzymes: Rifampin decreased Linagliptin exposure, suggesting that the
efficacy of Linagliptin may be reduced when administered in combination with a
strong P-gp inducer or CYP 3A4 inducer. As Linaptin M is a fixed-dose
combination of Linagliptin and Metformin, use of alternative treatments (not
containing Linagliptin) is strongly recommended when concomitant treatment with
a strong P-gp or CYP 3A4 inducer is necessary.
Drugs Affecting
Glycemic Control: Certain drugs tend
to produce hyperglycemia and may lead to loss of glycemic control. These drugs
include the thiazides and other diuretics, corticosteroids, phenothiazines,
thyroid products, estrogens, oral contraceptives, phenytoin, nicotinic acid,
sympathomimetics, calcium channel blocking drugs, and isoniazid. When such
drugs are administered to a patient receiving Linaptin M, the patient should be
closely observed to maintain adequate glycemic control. When such drugs are
withdrawn from a patient receiving Linaptin M, the patient should be observed
closely for hypoglycemia.
Contraindications
Although Linagliptin
undergoes minimal renal excretion, Metformin Hydrochloride is known to be
substantially excreted by the kidney. The risk of Metformin Hydrochloride accumulation
and lactic acidosis increases with the degree of renal impairment. Therefore,
this combination is contraindicated in patients with renal impairment. It is
also contraindicated in acute or chronic metabolic acidosis (diabetic
ketoacidosis) and in hypersensitivity to Linagliptin or Metformin
Hydrochloride.
Side Effects
Most common side
effects are nasopharyngitis and diarrhea. Hypoglycemia is more common in
patients treated with Linaptin M and sulfonylureas.
Pregnancy &
Lactation
There are no adequate
and well-controlled studies in pregnant women with this combination or its
individual component; so it should be used during pregnancy only if clearly
needed. Caution should also be excercised when it is administered to a
lactating mother.
Precautions &
Warnings
In a patient with
lactic acidosis who is taking Metformin, the drug should be discontinued
immediately and supportive therapy promptly instituted. There have been
postmarketing reports of acute pancreatitis. If pancreatitis is suspected,
promptly discontinue Linagliptin & Metformin. Temporarily discontinue
Linagliptin & Metformin in patients undergoing radiologic studies with
intravascular administration of iodinated contrast materials or any surgical
procedures necessitating restricted intake of food and fluids. Metformin may
lower Vitamin B12 levels; so hematologic parameters shoud be monitored
annually.
Under certain conditions, too much metformin can cause lactic acidosis. The
symptoms of lactic acidosis are severe and quick to appear, and usually occur
when other health problems not related to the medicine are present and are very
severe, such as a heart attack or kidney failure. Symptoms of lactic acidosis
include: abdominal or stomach discomfort, decreased appetite, diarrhea, fast or
shallow breathing, a general feeling of discomfort, muscle pain or cramping,
and unusual sleepiness, tiredness, or weakness. Be sure to drink extra fluids
when you exercise or increase your activity or if you have vomiting or
diarrhea. Pancreatitis may occur while you are using this medicine. Check with
your doctor right away if you have a sudden and severe stomach pain, chills,
constipation, nausea, vomiting, loss of appetite, a fever, or lightheadedness.
Need to temporarily stop taking this medicine before you have major surgery or
diagnostic tests including procedures that use contrast dye.
It is very important to carefully follow any instructions from your health care
team about:
Linagliptin and
metformin combination can cause hypoglycemia (low blood sugar). However, this
can also occur if you delay or miss a meal or snack, drink alcohol, exercise
more than usual, cannot eat because of nausea or vomiting, take certain
medicines, or take linagliptin and metformin combination with another type of
diabetes medicine. The symptoms of low blood sugar must be treated before they
lead to unconsciousness (passing out). Different people feel different symptoms
of low blood sugar. It is important that you learn which symptoms of low blood
sugar you usually have so you can treat it quickly.
Overdose Effects
In the event of an
overdose with Linaptin M the usual supportive measures (i.e. remove unabsorbed
material from the gastrointestinal tract, perform clinical monitoring, and
institute supportive treatment) should be employed. Removal of Linagliptin by
hemodialysis or peritoneal dialysis is unlikely but Metformin Hydrochloride is
dialyzable.
During controlled clinical trials in healthy subjects, with single doses of up
to 600 mg of Linagliptin (equivalent to 120 times the recommended daily dose),
there were no dose-related clinical adverse drug reactions.
Overdose of Metformin Hydrochloride has occurred in case of ingestion of
amounts greater than 50 grams. Hypoglycemia was reported in approximately 10%
of cases, but no causal association with Metformin Hydrochloride has been
established. Lactic acidosis has been reported in approximately 32% of
Metformin Hydrochloride overdose cases.
Therapeutic Class
Combination Oral
hypoglycemic preparations
Storage Conditions
Keep in a cool & dry place (below 30°C),
protected from light & moisture. Keep out of the reach of children.
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