Description
Latin name
Fervex
Release form
Fervex. Powder for oral solution (lemon without sugar).
Packaging
in 3 g sachets in a pack of cardboard 8 sachets.
Indications
It is used for acute respiratory infections, acute respiratory viral infections, rhinopharyngitis to alleviate the following symptoms:
rhinorrhea, nasal congestion
headache
increased body temperature srdlkr60 rhinophenia acute infections rhinopharyngitis to alleviate the following symptoms:
rhinorrhea, nasal congestion
headache
elevated body temperature
lacrimation
sneezing
Contraindications
hypersensitivity to the components of the
preparation erosive and ulcerative gastrointestinal tract lesions (in the acute phase)
renal failure
portal hypertension
chronic alcoholism
glucose deficiency childhood 15-year-old childhood 6-year-old lactation (breastfeeding).
Caution should be used in liver failure, angle-closure glaucoma, prostatic hyperplasia, congenital hyperbilirubinemia (Gilbert, Dubin-Johnson and Rotor syndromes), in case of viral hepatitis, alcoholic hepatitis, in elderly patients.
Use during pregnancy and lactation
The use of the drug is contraindicated in the I and III trimesters of pregnancy and during lactation (breastfeeding).
Ingredients
1 sachet contains:
Active ingredients:
paracetamol 500 mg,
pheniramine maleate 25 mg,
ascorbic acid 200 mg
Excipients, dry sodium chloride,
lemon rum (Antilles).
Dosage and administration of
Fervex is administered orally by 1 sachet 2-3 times / day, preferably between meals. The interval between doses of the drug is at least 4 hours.
In patients with impaired liver or kidney function and elderly patients, the interval between doses of the drug should be at least 8 hours.
The duration of treatment (without consulting a doctor) is not more than 5 days when used as an analgesic and not more than 3 days as an antipyretic.
The drug should be completely dissolved in a glass of warm water and drink the resulting solution immediately.
Side effects
The drug is well tolerated in recommended doses.
Possible dry mouth, nausea, vomiting, abdominal pain, impaired urination, constipation, allergic reactions (erythema, skin rash, itching, urticaria, Quincke’s edema, anaphylactic shock), drowsiness, accommodation disturbance, palpitations, orthostatic hypotension , impaired coordination, tremor, confusion, hallucinations, impaired concentration (more often in elderly patients).
Rarely – anemia, leukopenia, agranulocytosis, thrombocytopenia, agitation, nervousness, insomnia.
If you experience any adverse reactions, stop taking the drug and consult your doctor.
Drug Interaction
Antidepressants, antiparkinsonian agents, antipsychotics (phenothiazine derivatives) – increase the risk of side effects (urinary retention, dry mouth, constipation) of Fervex.
When used with Fervex, ACS increases the risk of developing glaucoma.
Inductors of microsomal oxidation in the liver (phenytoin, ethanol, barbiturates, rifampicin, phenylbutazone, tricyclic antidepressants) increase the production of hydroxylated active metabolites of paracetamol, which leads to the possibility of developing severe intooxication with more peroxidation.
Microsomal oxidation inhibitors (including cimetidine) reduce the risk of hepatotoxic action of paracetamol.
Paracetamol reduces the effectiveness of uricosuric drugs.
Ethanol promotes acute pancreatitis.
Ethanol enhances the sedative effect of antihistamines.
overdose
Symptoms due to the action of paracetamol: pallor of the skin, decreased appetite, nausea, vomiting, hepatonecrosis (the severity of necrosis due to intoxication depends directly on the degree of overdose). Toxic effect in adults is possible after taking paracetamol at a dose of more than 10-15 g: increased activity of hepatic transaminases, an increase in prothrombin time (after 12-48 h after administration) a detailed clinical picture of liver damage manifests itself in 1-6 days. Rarely, lightning development of liver failure, which may be complicated by renal failure (tubular necrosis).
Treatment: in the first 6 hours after overdose – gastric lavage, the introduction of donors of SH-groups and precursors for the synthesis of glutathione – methionine in 8-9 h after overdose and N-acetylcysteine after 12 h. , as well as the time elapsed since his admission.
Storage conditions
Keep out of the reach of children, in a dry place at a temperature not exceeding 25 ° C.
The Expiration of
is 3 years.
Deystvuyuschee substances
Paracetamol, Fenyramyn, ascorbic acid
dosage form
dosage form
powder for oral
Uppsala SAS, France
