Inosine Pranobex – Normomed tablets 500 mg 30 pcs

$26.00

Description

Release form

Tablets

Indications

Treatment of influenza and other acute respiratory viral infections

infections caused by herpes simplex virus type I and II: genital herpes and labial herpes, herpes keratitis, chicken pox, herpes zoster

papillomavirus infection: papilloma of the larynx / vocal cords (fibrous type), papillomavirus infection of the genital organs in men and women, warts

subacute sclerosing panencephalitis

molluscum contagiosum.

Contraindications

Hypersensitivity to inosine praiobex and other components of the drug

gout

urolithiasis

chronic renal failure

arrhythmias

pregnancy and lactation

up to 15 kg (20 kg) children weight.

Caution

Caution should be exercised when given concomitantly with xaptin oxidase inhibitors, diuretics, zidovudine, in acute liver failure. Use during pregnancy and the period of breastfeeding

Contraindicated in pregnant women and women who are breast-feeding, because the safety of the drug has not been investigated.

Special instructions

Consult with your doctor before starting treatment.

Normomed, like other antiviral agents, is most effective for acute viral infections if treatment is started at an early stage of the disease (preferably from the first day).

After 2 weeks of using the drug, you should monitor the concentration of uric acid in blood serum and urine.

With prolonged use after 4 weeks, it is advisable to monitor liver and kidney function every month (activity of ² њliver ² ќ transaminases in blood plasma, creatinine, uric acid).

Patients with a significantly increased concentration of uric acid in the body can simultaneously take drugs that lower its concentration. In the lobby of the treatment, it is necessary to control the concentration of uric acid in the blood serum when prescribing the drug simultaneously with drugs that increase the concentration of uric acid or drugs that impair renal function.

Normomed should be used with caution in patients with acute liver failure, since the drug is metabolized in the liver.

Effect on the ability to drive vehicles or work with mechanisms

The effect of the drug on the rate of psychomotor reactions has not been investigated. When using the drug, the possibility of dizziness and drowsiness should be considered.

Ingredients

1 tablet contains:

Active ingredient:

Inosine Pranobex 500.0 mg

Excipients:

Microcrystalline cellulose 33.5 mg

Perlitol flash (mannitol – 80% and corncrumd 20%) Sodium carboxymethyl starch 67.0 mg

Povidone K-17 10.0 mg

Magnesium stearate 6.0 mg

Dosage and administration

Tablets are taken orally after a meal with a little water. The recommended daily dose for adults and children aged 3 years and older (body weight over 15-20 kg) is 50 mg / kg body weight in 3-4 doses, which is on average for adults – 6-8 tablets per day, for children – 1/2 tablet per 5 kg of body weight per day. In severe forms of infectious diseases, the dose can be individually increased up to 100 mg / kg body weight per day, divided into 4-6 doses. The maximum daily dose for adults is 3-4 g / day, for children aged 3 years and older – 50 mg / kg / day.

Duration of treatment:

In acute diseases, the duration of treatment in adults and children is usually 5 to 14 days. Treatment should be continued for 2 days after the disappearance of clinical symptoms. If necessary, the duration of treatment can be increased individually under the supervision of a physician.

In chronic relapsing diseases, treatment in adults and children is carried out in several courses lasting 5-10 days at intervals of 8 days. During maintenance therapy, the dose can be reduced to 500-1000 mg / day (1-2 tablets) for 30 days.

For herpetic infections, adults and children are prescribed for 5-10 days before the symptoms disappear, in the asymptomatic period, 1 tablet 2 times a day for 30 days to reduce the number of relapses.

For papillomavirus infection, adults are prescribed 2 tablets 3 times a day for children, 1/2 tablets per 5 kg / body weight per day in 3-4 doses for 14-28 days as monotherapy.

In case of cervical dysplasia associated with human papillomavirus, 2 tablets are prescribed 3 times a day for 10 days, then 2-3 similar courses are carried out with an interval of 10-14 days.

In case of recurrent genital warts, adults are prescribed 2 tablets 3 times a day, for children 1/2 tablet per 5 kg / body weight per day in 3-4 doses per day, either as a mopotherapy or in combination with surgical treatment for 14-28 days, then with a three-fold repetition of the specified course at intervals of 1 month.

Use in elderly patients. The need for dose adjustment pet, the drug is used in the same way as in middle-aged patients. It should be borne in mind that in elderly patients, an increase in the concentration of uric acid in blood serum and urine is more likely than in middle-aged patients.

Use in patients with renal and hepatic insufficiency.

Against the background of treatment with Normomed, it is necessary to monitor the content of uric acid in blood serum and urine every 2 weeks. Monitoring the activity of liver enzymes is recommended every 4 weeks with long courses of treatment with the drug.

Side effects

The frequency of side effects after using the drug is classified according to WHO recommendations: frequent -> 1% and 0.1% and

From the nervous system: frequent – headache, dizziness, fatigue, poor health, weakness, infrequent – nervousness, drowsiness, insomnia.

From the gastrointestinal tract: frequent – decreased appetite, nausea, vomiting, epigastric pain infrequent – diarrhea, constipation.

From the liver and biliary tract: frequent temporary increase in the activity of transaminases and alkaline phosphatase in blood plasma, increased concentration of urea in blood plasma.

From the skin and subcutaneous tissues: frequent – itching, rash infrequent: maculopapular rash, urticaria, angioedema.

From the kidneys and urinary tract: infrequent – polyuria.

General disorders: frequent – joint pain, exacerbation of gout.

Laboratory and instrumental data: frequent – increased blood urea nitrogen concentration.

Drug Interactions

Immunosuppressants weaken the immunostimulating effect of the drug. The drug should be used with caution in patients taking simultaneously xytin oxidase inhibitors (allopurinol) or drugs capable of blocking the kayaltsy secretion of uric acid, for example, œloop diuretics (furosemide, torasemide, ethacryic acid), as this can lead to an increase in the concentration of uric acid in blood serum.

The combined use of the drug with zidovudine leads to an increase in the concentration of the latter in blood plasma and lengthens its T1 / 2 (if used together, dose adjustment of zidovudine may be required).

Overdose

In case of overdose gastric lavage and symptomatic therapy are indicated.

Storage conditions

In a dark place at a temperature of no higher than 30 ° C.

Keep out of the reach of children.

Expiration

3 years.

Form of Treatment

syrup