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Priglip-M 20/500 Tablet SR

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Prescription Required

Marketer

Primus Remedies Pvt Ltd

Salt Composition

Metformin (500mg) + Teneligliptin (20mg)

Overview Priglip-M 20/500 Tablet SR

Combiflex-DM 20/500 Extended-Release tablets combine two medications to effectively manage elevated blood glucose in individuals with type 2 diabetes. This dual action helps mitigate serious diabetic complications like renal impairment and vision loss, and may also lessen the risk of cardiovascular events. Combiflex-DM 20/500 ER may be administered independently or in conjunction with other antidiabetic therapies. Optimal results are achieved with adherence to a balanced diet and regular physical activity. Dosage is personalized based on your health status, glucose readings, and other concurrent medications. Ingesting the tablet with food minimizes gastrointestinal discomfort. Consistent daily dosing at the same time maximizes therapeutic benefits; discontinuation should only occur under medical supervision. This medication actively manages blood sugar, preventing future complications. Continued commitment to your prescribed diet and exercise regimen is crucial. Lifestyle choices significantly impact diabetes control. Common side effects include nausea, vomiting, diarrhea, abdominal distress, and headache. Hypoglycemia is a potential side effect, especially when combined with insulin or sulfonylureas; learn to identify and address this. This medication is not universally appropriate. Consult your physician prior to use if you have a history of kidney, liver, or heart disease, pancreatic issues, or significant alcohol consumption. Pregnant or lactating individuals should seek medical guidance. Inform your doctor of all medications you are taking to prevent potential drug interactions. Alcohol should be minimized due to its hypoglycemic effect. Your doctor will monitor kidney function and blood glucose levels throughout treatment.

Primary Ingredients of Priglip-M 20/500 Tablet SR

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Uses of Priglip-M 20/500 Tablet SR

Managing type 2 diabetes

Major Benefits of Priglip-M 20/500 Tablet SR:

Follow your doctor's instructions precisely regarding dosage and treatment length for Priglip-M 20/500 Tablet SR. Ingest the tablet whole; do not break, crush, or chew it. Administer this medication with a meal.

Common Side effects of Priglip-M 20/500 Tablet SR:

  • Nausea
  • Vomiting
  • Headache
  • Hypoglycemia (low blood glucose level)
  • Diarrhea

How to use Priglip-M 20/500 Tablet SR:

Administer this medication precisely as your physician directs, adhering to both the prescribed dosage and treatment length. Ingest the tablet whole; avoid chewing, crushing, or fracturing it. Consume Priglip-M 20/500 Tablet SR with a meal.

How Priglip-M 20/500 Tablet SR works:

Extended-release Priglip-M 20/500 tablets contain a dual antidiabetic medication formulation.

SAFETY ADVICE

AlcoholAlcoholUNSAFE

Combining Priglip-M 20/500 SR tablets with alcohol is not advisable due to safety concerns.

PregnancyPregnancyCONSULT YOUR DOCTOR

The use of Priglip-M 20/500 Tablet SR during pregnancy might pose risks. While human data is scarce, animal research indicates potential harm to the fetus. A physician will assess the advantages against possible risks prior to prescribing. Seek medical advice.

Breast feedingBreast feedingCONSULT YOUR DOCTOR

The extended-release Priglip-M 20/500 tablet is likely unsafe for breastfeeding mothers. Available human data indicates potential transfer to breast milk, posing a risk to the infant.

DrivingDrivingCONSULT YOUR DOCTOR

Priglip-M 20/500 Tablet SR's effect on driving ability is undetermined. Refrain from driving if you exhibit symptoms impairing concentration or reaction time.

KidneyKidneyCAUTION

Patients with kidney impairment should use Priglip-M 20/500 SR tablets cautiously, potentially requiring dosage modification. Physician consultation is necessary. Priglip-M 20/500 SR tablets are contraindicated in individuals with severe kidney disease. Routine monitoring of renal function is recommended during treatment.

LiverLiverUNSAFE

Use of Priglip-M 20/500 SR tablets is likely inadvisable for individuals with hepatic impairment and should be avoided. Medical advice is recommended.

What if you forget to take Priglip-M 20/500 Tablet SR :

Should you forget a dose of Priglip-M 20/500 Tablet SR, take it immediately if you remember. However, near the time for your next scheduled dose, omit the missed dose and resume your usual dosing pattern. Avoid taking a double dose.

Facts to Know About Priglip-M 20/500 Tablet SR

LabelValue
Developing Habits No.
Type of Therapy Diabetes Management

FAQs on Priglip-M 20/500 Tablet SR

Priglip-M 20/500 Tablet SR is safe when used as directed by your doctor. However, even with correct usage, you may experience side effects such as nausea, diarrhea, vomiting, stomach upset, headache, nasal congestion, sore throat, respiratory infection, and hypoglycemia (low blood sugar). Hypoglycemia is more likely if you're also taking insulin or sulfonylurea. Report any persistent issues to your doctor.
Priglip-M 20/500 SR tablets rarely cause hypoglycemia by themselves. However, low blood sugar can result from inadequate caloric intake while using this medication. Symptoms include nausea, headache, irritability, hunger, sweating, dizziness, rapid heartbeat, anxiety, and shakiness. These are more likely if meals are missed or delayed, alcohol is consumed, excessive exercise occurs, or other antidiabetic medications are taken concurrently. Regular blood sugar monitoring is therefore crucial. Carrying glucose tablets, honey, or fruit juice is advised.
Nausea and vomiting are possible side effects of Priglip-M 20/500 Tablet SR. If vomiting occurs, sip small amounts of water or other fluids frequently. Consult your doctor if vomiting continues or you experience dehydration symptoms such as dark, strong-smelling urine and infrequent urination. Do not take other medications without your doctor's approval.
Patients with known allergies to Priglip-M 20/500 Tablet SR components or excipients should not use this medication. Its use is contraindicated in patients with severe kidney or liver impairment, congestive heart failure, lactic acidosis, or diabetic ketoacidosis.
Priglip-M 20/500 Tablet SR can cause lactic acidosis (MALA, or Metformin-associated lactic acidosis), a rare but serious side effect resulting from excessive blood lactic acid. This risk is heightened in individuals with kidney disease, the elderly, or those who consume significant amounts of alcohol; therefore, its use is avoided in these groups. Symptoms include muscle pain or weakness, dizziness, fatigue, cold extremities, shortness of breath, nausea, vomiting, abdominal pain, and bradycardia. If these occur, discontinue Priglip-M 20/500 Tablet SR immediately and seek medical attention.
Prolonged use of Priglip-M 20/500 SR tablets can lead to vitamin B12 deficiency by hindering its absorption in the stomach. This deficiency may result in anemia, neurological issues such as tingling, numbness in extremities, weakness, urinary problems, cognitive changes, and balance difficulties (ataxia). If you experience any of these symptoms, consult your doctor for B12 level monitoring and potential supplementation.
Store this medication in its original, tightly closed container, following the storage instructions on the label. Discard any unused medication. Keep it out of reach of children, pets, and others.
Priglip-M 20/500 Tablet S...
105
MRP 128
17% off