Essentiale Forte 50 capsules Liver Detox Cleanse Regeneration Health Support - contains Soy Essential Phospholipids Non-GMO

Product Information

Raportand reactiile adverse, puteti contribui la furnizarea de informatii suplimentare privind siguranta acestui medicament.

Agitation, coma, convulsion, cough, depression, dysesthesia, dizziness, hallucinations, nervousness, paresthesia, somnolence, thinking abnormality, and tremor. Respiratory System There are no reports of pregnant women having been treated with Essentiale Forte® (amphotericin b). Teratogenic Effects. Pregnancy Category B: Reproductive studies in rats and rabbits at doses of Essentiale Forte® (amphotericin b) up to 0.64 times the human dose revealed no harm to the fetus. Because animal reproductive studies are not always predictive of human response, and adequate and well-controlled studies have not been conducted in pregnant women, Essentiale Forte® (amphotericin b) should be used during pregnancy only after taking into account the importance of the drug to the mother. Nursing Mothers NOTE: An existing intravenous line must be flushed with 5% Dextrose Injection prior to infusion of Essentiale Forte. If this is not feasible, Essentiale Forte must be administered through a separate line.

Vaisto sudėtyje yra sojų aliejaus, kuris gali sukelti sunkių alerginių reakcijų. Jei esate alergiškas (alergiška) žemės riešutams arba sojai, Jums šio vaisto vartoti negalima.

The effect of Essentiale Forte on renal and hepatic function and on serum electrolytes was assessed from laboratory values measured repeatedly in Study 94-0-002. The frequency and magnitude of hepatic test abnormalities were similar in the Essentiale Forte and amphotericin B groups. Nephrotoxicity was defined as creatinine values increasing 100% or more over pretreatment levels in pediatric patients, and creatinine values increasing 100% or more over pretreatment levels in adult patients provided the peak creatinine concentration was > 1.2 mg/dL. Hypokalemia was defined as potassium levels ≤ 2.5 mmol/L any time during treatment. The incidence of common adverse events (incidence of 10% or greater) occurring with Essentiale Forte compared to amphotericin B deoxycholate, regardless of relationship to study drug, is shown in the following table:Many drugs are excreted in human milk. However, it is not known whether Essentiale Forte is excreted in human milk. Due to the potential for serious adverse reactions in breast-fed infants, a decision should be made whether to discontinue nursing or whether to discontinue the drug, taking into account the importance of the drug to the mother. Pediatric Use Veoma retko (mogu da se jave kod najviše 1 na 10000 pacijenata koji uzimaju lek): alergijske reakcije daca sunteti alergic la preparate din seminte de soia sau la oricare dintre celelalte componente ale acestui medicament (enumerate la punctul 6).

Vienkartinė dozė: dvi kietosios kapsulės (600 mg sojų fosfolipidų). Paros dozė: po dvi kietąsias kapsules tris kartus per parą (1800mg sojų fosfolipidų). The pharmacokinetics of amphotericin B after the administration of Essentiale Forte® (amphotericin b) are nonlinear. Volume of distribution and clearance from blood increase with increasing dose of Essentiale Forte® (amphotericin b) , resulting in less than proportional increases in blood concentrations of amphotericin B over a dose range of 0.6-5 mg/kg/day. The pharmacokinetics of amphotericin B in whole blood after the administration of Essentiale Forte® and amphotericin B desoxycholate are: Day 1 body temperature increased above the temperature taken within 1 hour prior to infusion (preinfusion temperature) or above the lowest infusion value (no preinfusion temperature recorded).

Pediatric patients, age 1 month to 16 years, with presumed fungal infection (empirical therapy), confirmed systemic fungal infections or with visceral leishmaniasis have been successfully treated with Essentiale Forte. In studies which included 302 pediatric patients administered Essentiale Forte, there was no evidence of any differences in efficacy or safety of Essentiale Forte compared to adults. Since pediatric patients have received Essentiale Forte at doses comparable to those used in adults on a per kilogram body weight basis, no dosage adjustment is required in this population. Safety and effectiveness in pediatric patients below the age of one month have not been established. (See Description Of Clinical Studies - Empirical Therapy in Febrile Neutropenic Patients and DOSAGE AND ADMINISTRATION). Elderly Patients vaistas, kaip ir visi kiti, gali sukelti šalutinį poveikį, nors jis pasireiškia ne visiems žmonėms. dacă sunteţi alergic la preparate din seminţe de soia sau la oricare dintre celelalte componente ale acestui medicament. Dacă după 30 zile nu vă simţiţi mai bine sau vă simţiţi mai rău, trebuie să vă adresaţi unui medic. Ce medicamente ati recomanda pt.edemele gambiere aparute la o femeie de aproape 78 de ani care are A ...

Daca dupa 30 zile nu va simtiti mai bine sau va simtiti mai rau, trebuie sa va adresati unui medic. Essentiale forte N se koristi u cilju ublažavanja subjektivnih tegoba, kao što je nedostatak apetita, ili Directions for Reconstitution, Filtration and Dilution Read This Entire Section Carefully Before Beginning Reconstitution Essentiale Forte must be reconstituted using Sterile Water for Injection, USP (without a bacteriostatic agent). Vials of Essentiale Forte containing 50 mg of amphotericin B are prepared as follows: Reconstitution La noi, prețul afișat este valabil atât pentru comenzile online cât și pentru toate locațiile noastre.

Side Effects

Visada vartokite šį vaistą tiksliai kaip aprašyta šiame lapelyje arba kaip nurodė gydytojas arba vaistininkas. Hyperbilirubinaemia, Hypokalaemia, Electrolyte imbalance including blood potassium increased, blood magnesium decreased