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Furoped 10 MG Solution
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Furoped 10 MG Solution

Manufactured bySamarth Life Sciences Pvt. Ltd.
ContainsFurosemide
Description
Furoped 10 MG Solution is a diuretic (water pill), used to control high blood pressure and fluid retention. It is usually taken once daily preferably in the daytime to prevent sleep disturbances. Frequent monitoring of blood pressure and electrolytes level is necessary while taking this medicine.
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Side effectsConcernsUsage

Side effects

Major & minor side effects for Furoped 10 MG Solution

  • Low potassium and magnesium
  • Decreased calcium level
  • Hearing impairment
  • Headache
  • Weakness
  • Increased sensitivity of the skin to sunlight
  • Muscle spasm
  • Skin rash

Uses of Furoped 10 MG Solution

What is it prescribed for?

  • Hypertension
  • Congestive Heart Failure
  • Edema
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Concerns

Commonly asked questions

  • How long does it take for this medicine to take effect?
    The effect of this medicine can be observed within 30 to 60 minutes of administration of the dose.
  • How long do the effects of this medicine last?
    The effect of this medicine lasts for an average duration of 6 to 8 hours.
  • Is it safe to consume alcohol while taking this medicine?
    Consumption of alcohol is not recommended during treatment with this medicine due to the increased risk of side effects such as dizziness, lightheadedness, and fainting. It is advised that you do not perform any activities that require high mental alertness such as driving a vehicle or operating machinery if you consume alcohol during treatment with this medicine.
  • Is this a habit forming medicine?
    No habit forming tendency has been reported.
  • Can this medicine be taken during pregnancy?
    This medicine is not recommended for use in pregnant women unless absolutely necessary. All the risks and benefits should be discussed with the doctor before taking this medicine.
  • Can this medicine be taken while breast-feeding?
    This medicine is not recommended for use in breastfeeding women unless absolutely necessary. All the risks and benefits should be discussed with the doctor before taking this medicine. Your doctor may advise you to discontinue breastfeeding or to discontinue the drug based on your clinical condition.

Allergy

This medicine is not recommended for use in patients with a known allergy to furosemide, or any other inactive ingredients present in the formulation.

Anuria

This medicine is not recommended for use in patients with anuria, a condition where the kidney is unable to produce urine.
Warnings for special population

Pregnancy

This medicine is not recommended for use in pregnant women unless absolutely necessary. All the risks and benefits should be discussed with the doctor before taking this medicine.

Breast-feeding

This medicine is not recommended for use in breastfeeding women unless absolutely necessary. All the risks and benefits should be discussed with the doctor before taking this medicine. Your doctor may advise you to discontinue breastfeeding or to discontinue the drug based on your clinical condition.
General warnings

Severe liver injury with cirrhosis and ascites

This medicine should be used with caution in the patients suffering from liver diseases such as severe liver injuries, cirrhosis, ascites, etc. since it may worsen the patient's condition. Close monitoring of electrolytes levels and liver function is recommended for such patients. Appropriate dose adjustments or replacement with a suitable alternative may be required based on the clinical condition.

Volume depletion and electrolyte imbalance

This medicine may alter the blood volume and electrolyte levels in some patients. This may cause dizziness, dry mouth, and acid-base imbalance. This risk is especially higher in patients suffering from kidney and liver diseases. Close monitoring of blood pressure and electrolyte levels is recommended for such patients. Appropriate dose adjustments or replacement with a suitable alternative may be required based on the clinical condition.

Hearing problem

This medicine may increase the risk of developing a hearing problem when rapid intravenous injections are given. This risk is especially higher in patients receiving other medicines which may cause an adverse effect on the hearing. Any symptoms such as hearing difficulties, ringing in the ears, etc. should be reported to the doctor immediately. Replacement with a suitable alternative may be required in some cases based on the clinical condition.

Driving or operating machinery

This medicine may cause dizziness in some patients. It is advised that you do not perform any activities that require high mental alertness such as driving a vehicle or operating machinery if you experience any dizziness during treatment with this medicine.

Missed Dose

Take/Administer the missed dose as soon as you remember. If it is almost the time for your next dose, skip the missed dose. Do not double your dose to make up for the missed dose.

Overdose

Seek emergency medical treatment or contact the doctor in case of an overdose.
All drugs interact differently for person to person. You should check all the possible interactions with your doctor before starting any medicine.
Interaction with Alcohol

Description

N/A

Instructions

Consumption of alcohol is not recommended during treatment with this medicine due to the increased risk of side effects such as dizziness, lightheadedness, and fainting. It is advised that you do not perform any activities that require high mental alertness such as driving a vehicle or operating machinery if you consume alcohol during treatment with this medicine.
Interaction with Medicine

Nonsteroidal anti-inflammatory drugs

Aminoglycoside antibiotics

Angiotensin converting enzyme inhibitors (ACEI's)

Antidepressants

Disease interactions

Diabetes

This medicine should be used with caution in patients with diabetes due to the increased risk of altered blood glucose levels. Close monitoring of blood glucose levels is necessary during therapy with this medicine. Appropriate corrective measures, dose adjustments, or replacement with a suitable alternative may be required based on the clinical condition.

Kidney Disease

This medicine is not recommended for use in patients with a known history of kidney diseases due to the increased risk of worsening of the patient's condition. Renal function should be assessed before initiating treatment. Replacement with a suitable alternative may be necessary based on the clinical condition.
Food interactions
Information not available.
Lab interactions
Information not available.
This is not an exhaustive list of possible drug interactions. You should consult your doctor about all the possible interactions of the drugs you’re taking.
Take/Administer this medicine as advised by your doctor. Do not take/administer in larger amounts than prescribed. It is advised to take this medicine in the daytime to prevent sleep disturbance. Drink an adequate amount of water. Close monitoring of kidney function and electrolyte levels is necessary during treatment with this medicine. Report any undesired side effects to the doctor. Do not stop the use of this medicine without consulting your doctor.
Miscelleneous

Can be taken with or without food, as advised by your doctor

To be taken as instructed by doctor

May cause sleepiness

How it works
It works by increasing the excretion of water and sodium by preventing its reabsorption in the kidneys.
Legal Status

Approved

Approved

Unknown

Approved

Classification

Category

Loop diuretics

Schedule

Schedule H

Furosemide: MedlinePlus Drug Information [Internet]. Medlineplus.gov. 2020 [cited 24 April 2020]. Available from:

https://medlineplus.gov/druginfo/meds/a682858.html

Furosemide - DrugBank [Internet]. Drugbank.ca. 2020 [cited 24 April 2020]. Available from:

https://www.drugbank.ca/drugs/DB00695

Furosemide [Internet]. Pubchem.ncbi.nlm.nih.gov. 2020 [cited 24 April 2020]. Available from:

https://pubchem.ncbi.nlm.nih.gov/compound/Furosemide

[Internet]. Medicines.org.uk. 2020 [cited 24 April 2020]. Available from:

https://www.medicines.org.uk/emc/files/pil.109.pdf
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Information on this page was last updated on 19 May 2020

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