Febricet - instructions for use, dose, side effects, contraindications

Excipients: citric acid anhydrous - 100.0 mg, isomalt - 3035.0 mg, sodium saccharin - 28.0 mg, aroma lemon honey - 100.0 mg, silicon dioxide colloid anhydrous -12.0 mg.

Description:

Powder for solution for oral administration - powder from white to yellowish white with the smell of honey and lemon.

The prepared solution - slightly clouded, with the smell of lemon and honey.

Pharmacotherapeutic group:ARI and "colds" of symptoms remedy (analgesic non-narcotic means + H1-histamine receptor blocker + vitamin)

ATX: & nbsp

N.02.B.E Anilides

N.02.B.E.51 Paracetamol in combination with other drugs, excluding psycholeptics

Pharmacodynamics:

Combined drug.

Paracetamol has antipyretic and analgesic effect: reduces pain syndrome, which is observed in colds - sore throat, headache, muscle and joint pain, reduces heat.

Pheniramine has anti-allergic action: it removes the itch of the eyes, nose and throat, swelling and flushing of the mucous membranes of the nasal cavity, nasopharynx and paranasal sinuses, reduces rhinorrhea and lacrimation.

Ascorbic acid (vitamin C) replenishes the increased need for vitamin C for colds and flu, especially in the initial stages of the disease. Increases the body's resistance to infectious diseases.

Indications:

Symptomatic treatment of "colds", flu, ARVI (febrile syndrome, pain syndrome, rhinorrhea).

Contraindications:

Hypersensitivity to paracetamol and other components that make up the drug; taking other drugs containing substances that are part of the Fabricet®; portal hypertension, alcoholism, pregnancy, lactation; children's age (up to 15 years).

Carefully:

Bronchial asthma, chronic obstructive pulmonary disease, glucose-6-phosphate dehydrogenase deficiency, blood diseases, congenital hyperbilirubinemia (Gilbert syndrome, Dubin-Johnson syndrome and Rotor syndrome), erosive ulcerative gastrointestinal lesions, hyperoxalaturia, hepatic and / or renal insufficiency, glaucoma, prostatic hyperplasia.

Dosing and Administration:

Inside.

The contents of 1 packet should be dissolved in a glass of warm water and drunk after end of foaming. Take the drug with a lot of liquid, 1-2 hours after eating.

If the doctor does not give other instructions, then when using the drug, the following dosages should be observed.

Adults and children over 15 years of age should take 1 packet of powder 2-3 times a day. The maximum daily dose is 3 sachets.

The interval between doses should be 4-6 hours.

With CRF (SC 10 ml / min), the interval between doses should be more than 8 hours.

The maximum duration of treatment for children is 3 days.

Do not take the drug for more than 5 days without consulting a doctor.

Side effects:

Allergic reactions (incl.skin rash, itching, urticaria, angioedema, anaphylactic shock), headache, dizziness, sleep disorders, increased excitability, decreased speed of psychomotor reaction, nausea, vomiting, epigastric pain; dry mouth; retention of urine; paresis of accommodation; bronchial obstruction, anemia, thrombocytopenia, agranulocytosis.

With long-term use in large doses - hepatotoxic effect, hemolytic anemia, aplastic anemia, methemoglobinemia, pancytopenia, erosive-ulcerative lesions of the gastrointestinal tract, bleeding in the gastrointestinal tract, nephrotoxicity (papillary necrosis).

Overdose:

Conditioned, as a rule, paracetamol, manifested after taking more than 10-15 g of the latter.

Possible: pallor of the skin, anorexia, nausea, vomiting; hepatonecrosis; an increase in the activity of "hepatic" transaminases, an increase in prothrombin time.

When overdosing, it is urgent to see a doctor.

Treatment: gastric lavage followed by administration of activated charcoal; symptomatic therapy, the introduction of methionine after 8-9 hours after an overdose and N-acetylcysteine - after 12 h.

Interaction:

Strengthens the effects of sedatives, ethanol.

Antidepressants, antiparkinsonics, antipsychotics, phenothiazine derivatives - increase the risk of urinary retention, dry mouth, constipation.

Glucocorticosteroids increase the risk of developing glaucoma.

Paracetamol reduces the effectiveness of uricosuric medicines.

Phenyramin simultaneously with MAO inhibitors, furazolidone can lead to hypertensive crisis, agitation, hyperpyrexia.

With the simultaneous administration of the drug with barbiturates, diphenin, carbamazepine, rifampicin and other inducers of microsomal oxidation (phenytoin, ethanol, phenylbutazone, tricyclic antidepressants) increases the production of hydroxylated active metabolites and increases the risk of hepatotoxic effects of paracetamol in small overdoses.

Inhibitors of microsomal oxidation (cimetidine) reduce the risk of hepatotoxic effects.

Special instructions:During treatment should refrain from taking alcohol, sleeping pills and anxiolytic (tranquilizers) medicines.

Do not take with other medicines containing paracetamol.

If the symptoms do not go away within 3-5 days, consult a doctor.

Effect on the ability to drive transp. cf. and fur:Care should be taken when performing work that requires concentration of attention, increased speed of motor and mental reactions.

Form release / dosage:Powder for solution for oral administration, 500 mg + 25 mg + 200 mg.

Packaging:

4 grams of powder in a bag of combined material (paper, aluminum foil and polyethylene).

For 8 bags with instructions for use in a pack of cardboard.

Storage conditions:

Store in a dry place, at a temperature of 15 to 25 ° C.

Keep out of the reach of children.

Shelf life:

2 years.

Do not use after the expiration date printed on the package.

Terms of leave from pharmacies:Without recipe

Registration number:LSR-005755/08

Date of registration:22.07.2008

Expiration Date:Unlimited

The owner of the registration certificate:Hemofarm ADHemofarm AD Serbia

Manufacturer: & nbsp

HEMOFARM, A.D. Serbia

Representation: & nbspHEMOFARM A.D. HEMOFARM A.D. Serbia

Information update date: & nbsp06.01.2017

Illustrated instructions

Instructions

Febricet (Febricet)