Indications
This 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 Linatab 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 Linatab 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 Linatab 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 Linatab M, the patient should be closely observed to maintain
adequate glycemic control. When such drugs are withdrawn from a patient
receiving Linatab 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 Linatab 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:
Alcohol: Drinking alcohol may
cause severe low blood sugar.
Other medicines: This especially
includes nonprescription medicines such as aspirin, and medicines for appetite
control, asthma, colds, cough, hay fever, or sinus problems.
Counseling: Other family members
need to learn how to prevent side effects or help with side effects if they
occur.
Travel: Keep a recent
prescription and your medical history with you. Make allowances for changing time
zones and keep your meal times as close as possible to your usual meal times.
In case of emergency: There may
be a time when you need emergency help for a problem caused by your diabetes.
You need to be prepared for these emergencies. It is a good idea to wear a
medical identification (ID) bracelet or neck chain at all times. Also, carry an
ID card in your wallet or purse that says you have diabetes and that lists all
of your medicines.
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
Linatab 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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