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Furantoina

Generic name: Nitrofurantoin

Brand name: Macrodantin, Furantoina , Macrobid

Why is Furantoina prescribed?

Furantoina, an antibacterial drug, is prescribed for the treatment of urinary tract infections caused by certain strains of bacteria.

Most important fact about Furantoina

Breathing disorders have occurred in people taking Furantoina. Furantoina can cause inflammation of the lungs marked by coughing, difficulty breathing, and wheezing. It has also been known to cause pulmonary fibrosis (an abnormal increase in fibrous tissue of the lungs). This condition can develop gradually without symptoms and can be fatal. An allergic reaction to Furantoina is also possible and may occur without warning. Symptoms include a feeling of ill health and a persistent cough. However, all these reactions occur rarely and generally in those receiving Furantoina therapy for 6 months or longer.

Sudden and severe lung reactions are characterized by fever, chills, cough, chest pain, and difficulty breathing. These acute reactions usually occur within the first week of treatment and subside when therapy with Furantoina is stopped.

Your doctor should monitor your condition closely, especially if you are receiving long-term treatment with Furantoina.

How should you take Furantoina?

To improve absorption of the drug, Furantoina should be taken with food.

Follow your doctor's instructions carefully. Take the full amount prescribed, even if you are feeling better.

Furantoina works best if your urine is acidic. Ask your doctor whether you should be taking special measures to assure its acidity.

Furantoina may turn the urine brown.

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If you miss a dose of Furantoina

Take the forgotten dose as soon as you remember, then space out the rest of the day's doses at equal intervals.

Storage instructions for Furantoina

Store at room temperature. Protect from light and keep the container tightly closed.

What side effects may occur when taking Furantoina?

Side effects of Furantoina cannot be anticipated. If any develop or change in intensity, inform your doctor as soon as possible. Only your doctor can determine if it is safe for you to continue taking Furantoina.

More common side effects of taking Furantoina may include:

Lack or loss of appetite, nausea, vomiting

Less common or rare side effects of taking Furantoina may include:

Abdominal pain/discomfort, blue skin, chills, confusion, cough, chest pain, depression, diarrhea, difficulty breathing, dizziness, drowsiness, exaggerated sense of well-being, eye disorder, fever, hair loss, headache, hepatitis, hives, inflammation of the nerves causing symptoms of numbness, tingling, pain, or muscle weakness, intestinal inflammation, involuntary eye movement, irregular heartbeat, itching, itchy red skin patches, joint pain, muscle pain, peeling skin, psychotic reactions, rash, severe allergic reactions, skin inflammation with flaking, skin swelling or welts, vertigo, yellowing of the skin and whites of the eyes, weakness. Why should Furantoina not be prescribed ?

If you are sensitive to or have ever had an allergic reaction to nitrofurantoin or other drugs of this type, such as Furoxone, you should not take Furantoina. Make sure that your doctor is aware of any drug reactions that you have experienced.

Unless you are directed to do so by your doctor, do not take Furantoina if you have poor kidneys, producing little or no urine.

Furantoina should not be taken at term of pregnancy or during labor and delivery; it should not be given to infants under 1 month of age.

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Special warnings about Furantoina

Tell your doctor if you have any unusual symptoms while you are taking Furantoina.

Fatalities have been reported from hepatitis (liver disease) during treatment with nitrofurantoin. Long-lasting, active hepatitis can develop without symptoms; therefore, if you are receiving long-term treatment with this drug, your doctor should test your liver function periodically.

Fatalities from peripheral neuropathy,a disease of the nerves,have also been reported in people taking Furantoina. Conditions such as a kidney disorder, anemia, diabetes mellitus, a debilitating disease, or a vitamin B deficiency make peripheral neuropathy more likely. If you develop symptoms such as muscle weakness or lack of sensation, check with your doctor immediately.

If you experience diarrhea, tell your doctor. It may be a sign of serious intestinal inflammation.

Hemolytic anemia (destruction of red blood cells) has occurred in people taking Furantoina.

Continued or prolonged use of Furantoina may result in growth of bacteria that do not respond to it. This can cause a renewed infection, so it is important that your doctor monitor your condition on a regular basis.

Possible food and drug interactions when taking Furantoina

If Furantoina is taken with certain other drugs, the effects of either could be increased, decreased, or altered.

It is especially important to check with your doctor before combining Furantoina with the following:

Magnesium trisilicate (Gaviscon Antacid Tablets)
The gout drugs probenecid and sulfinpyrazone and other drugs that increase the amount of uric acid in the urine

Special information if you are pregnant or breastfeeding

The safety of Furantoina during pregnancy and breastfeeding has not been established. Furantoina does appear in human breast milk. If you are pregnant or breastfeeding or you plan to become pregnant or breastfeed, inform your doctor immediately.

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Recommended dosages for Furantoina

Treatment with Furantoina should be continued for 1 week or for at least 3 days after obtaining a urine specimen free of infection. If your infection has not cleared up, your doctor should re-evaluate your case.

ADULTS

The recommended dosage of Furantoina is 50 to 100 milligrams taken 4 times a day. For long-term treatment, your doctor may reduce your dosage to 50 to 100 milligrams taken at bedtime.

CHILDREN

Furantoina should not be prescribed for children under 1 month of age.

The recommended daily dosage of Furantoina for infants and children over 1 month of age is 5 to 7 milligrams per 2.2 pounds of body weight, divided into 4 doses over 24 hours.

For the long-term treatment of children, the doctor may prescribe daily doses as low as 1 milligram per 2.2 pounds of body weight taken in 1 or 2 doses per day.

The dosage of Furantoina for children over 12 years of age is one 100 milligram capsule every 12 hours for 7 days. Safety and effectiveness have not been established for children under 12.

OLDER ADULTS

Doctors tend to prescribe lower doses of Furantoina for older adults. Furantoina is more likely to cause lung and liver problems in members of this group; and because more older adults have poor kidneys, the risk of toxic reactions to Furantoina is also greater.

Overdosage of Furantoina

An overdose of Furantoina does not cause any specific symptoms other than vomiting. If vomiting does not occur soon after an excessive dose, it should be induced.

If you suspect an overdose of Furantoina, seek emergency medical treatment immediately.

 

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