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Monica Clark Pasadena monica3clark.exblog.jp

Mushrooms 26

Nitrofurantoin® or Furamag®, what to choose?

Encapsulated Furamag surpasses nitrofurantoin® in the spectrum of antimicrobial action, therefore, the list of indications for its use includes more diseases.

In particular, it is active against some protozoa, which makes it possible to treat gynecological infections..

This should be taken into account when choosing a medicine, and in general, nitrofurantoin® is more suitable for treating infections of MVP, moreover, it is much cheaper.

Nitrofurantoin® or Furamag®, what to choose?

Encapsulated Furamag is superior to nitrofurantoin® in the spectrum of antimicrobial action, therefore, more diseases are included in the list of indications for its use. In particular, it is active against some protozoa, which makes it possible to treat gynecological infections. nitrofurantoin online This should be taken into account when choosing a medicine, and in general, nitrofurantoin® is more suitable for treating infections of MVP, moreover, it is much cheaper.

special instructions

In patients with anemia, electrolyte imbalance, kidney disease, and deficiency of B vitamins, the likelihood of peripheral neuropathy increases.

The substance is ineffective in the treatment of diseases of the cortical substance of the kidneys, prostatitis, purulent paranephritis.

Nitrofurantoin should not be combined with drugs that have an inactive effect on kidney function.

The drug should not be prescribed to children under the age of one month. For the treatment of children, dosage adjustment is necessary.

> During pregnancy and lactation

The substance should not be taken by lactating and pregnant women.

Pharmacodynamics and pharmacokinetics

This substance inhibits the synthesis of deoxyribonucleic and ribonucleic acids, proteins, reduces the permeability of membranes and the intensity of aerobic metabolism of harmful bacteria.

The medicine has a wide spectrum of action, the agent is effective against gram-negative or gram-positive bacteria.

The drug inhibits vital activity: streptococci, staphylococci, Shigella dysenteriae, Shigella boydii, Escherichia coli, Shigella flexneri, Shigella sonnei, Proteus spp.

The drug has a high absorption capacity. http://medlineplus.gov/druginfo/meds/a682291.html After the penetration of the substance into the digestive tract, the bioavailability of the agent is about 50%. Eating increases the bioavailability of a substance.

The smaller the crystals of a chemical compound, the better they dissolve and penetrate into the systemic circulation. The microcrystalline form is absorbed faster and reaches a maximum concentration in the urine in a shorter period of time. About 60% binds to plasma proteins.

The substance undergoes metabolism in the tissues of the muscles of the liver. The elimination half-life makes from 20 to 25 minutes.

The drug overcomes the BBB, crosses the placenta, and is excreted in breast milk. The drug does not accumulate in the body and is completely excreted by the kidneys, about 40% - unchanged.


by monica3clark | 2020-09-15 16:58