Inhouse product
Indications
Emfogen is indicated
in:
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Pharmacology
Empagliflozin is a
sodium glucose co-transporter-2 (SGLT-2) inhibitor. SGLT2 co-transporters are
responsible for reabsorption of glucose from the glomerular filtrate in the
kidney. The glucuretic effect resulting from SGLT2 inhibition reduces renal
absorption and lowers the renal threshold for glucose, resulting in increased
glucose excretion. Additionally, it contributes to reduced hyperglycaemia,
assists weight loss, and reduces blood pressure.
Dosage &
Administration
The recommended dose
of Empagliflozin is 10 mg once daily, taken in the morning, with or without
food. In patients tolerating Empagliflozin, the dose may be increased to 25 mg
once daily. In patients with volume depletion, correcting this condition prior
to initiation of Empagliflozin is recommended.
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Interaction
Diuretics: Co-administration of Emfogen with diuretics
resulted in increased urine volume.
Insulin or Insulin
Secretagogues: Co-administration of
Emfogen with insulin or insulin secretagogues increases the risk for
hypoglycemia.
Positive Urine Glucose
Test: Monitoring glycemic
control with urine glucose tests is not recommended in patients taking SGLT2
inhibitors as SGLT2 inhibitors increase urinary glucose excretion and will lead
to positive urine glucose tests. Use alternative methods to monitor glycemic
control.
Interference with 1,5-anhydroglucitol
(1,5-AG) Assay: Monitoring glycemic
control with 1,5-AG assay is not recommended as measurements of 1,5-AG are
unreliable in assessing glycemic control in patients taking SGLT2 inhibitors.
Use alternative methods to monitor glycemic control.
Contraindications
Empagliflozin is
contraindicated in patients with history of serious hypersensitivity reaction
to Empagliflozin or any of its ingredients, severe renal impairment, end-stage
renal disease, or dialysis.
Side Effects
The most common adverse
reactions associated with Emfogen are urinary tract infections and female
genital mycotic infections. Others common side effects includes dehydration,
hypotension, weakness, dizziness and increased thirstiness.
Pregnancy &
Lactation
There are no adequate
and well-controlled studies of Empagliflozin in pregnant women. Empagliflozin
should be used during pregnancy only if the potential benefit justifies the
potential risk to the fetus. It is not known if Empagliflozin is excreted in
human milk. It is not recommended when breastfeeding.
Precautions &
Warnings
Assessment of renal
function is recommended prior to initiation of Emfogen and periodically
thereafter. Emfogen should not initiated in patients with an eGFR less than 45
ml/min/1.73 m2. No dose adjustment is needed in patients with an
eGFR greater than or equal to 45 ml/min/1.73 m2.
Overdose Effects
In the event of an
overdose with Emfogen the usual supportive measures (e.g., remove unabsorbed
material from the gastrointestinal tract, perform clinical monitoring, and
institute supportive treatment) should be employed. Removal of Emfogen by
hemodialysis has not been studied.
Therapeutic Class
Sodium-glucose
Cotransporter-2 (SGLT2) Inhibitors
Storage Conditions
Keep in a cool & dry
place (below 30° C), protected from light & moisture. Keep out of the reach
of children.
Chemical Structure
|
Molecular Formula : |
C23H27ClO7 |
|
Chemical Structure : |
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Common Questions about Emfogen 25 mg Tablet
What is Emfogen 25 mg Tablet?
Emfogen 25 mg Tablet is a SGLT-2 inhibitor
which reduces the reabsorption of glucose from kidney.
What is Emfogen 25 mg Tablet used for?
Emfogen 25 mg Tablet is commonly used to
improve glycemic control in adults.
Are there any pregnancy warnings?
Emfogen 25 mg Tablet may be unsafe to use
during pregnancy.
Are there any breast-feeding warnings?
Emfogen 25 mg Tablet is probably unsafe to use
during breastfeeding.
Does this affect kidney function?
Emfogen 25 mg Tablet should be used cautiously
in patients with an underlying kidney disease.
Does this affect liver function?
No dose adjustment is needed for patients with
the mild to moderate liver disease.
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