سعر Amoxicid 125 mg/5 ml suspension 60 ml 2026

Amoxicillin 125 mg/5 ml oral suspension, 60 ml bottle; aminopenicillin antibiotic.

• Infections of the ear, nose and throat, genitourinary tract, skin and skin structure, and lower respiratory tract due to susceptible (beta-lactamase-negative) isolates of designated bacteriaPopulation: Adults and pediatric patientsDailyMed (U.S. National Library of Medicine)
• Helicobacter pylori infection and duodenal ulcer disease in adults, in triple therapy with clarithromycin and lansoprazole or dual therapy with lansoprazolePopulation: AdultsDailyMed (U.S. National Library of Medicine)

• Most common adverse reactions (>1%) in clinical trials of capsules, tablets or oral suspension: diarrhea, rash, vomiting and nausea.International label, equivalent formulation · DailyMed (U.S. National Library of Medicine)
• Postmarketing reports include mucocutaneous candidiasis, hemorrhagic/pseudomembranous colitis, hypersensitivity reactions including anaphylaxis, serum sickness-like reactions, SJS/TEN/DRESS/AGEP, hepatic dysfunction including cholestatic jaundice, crystalluria and blood dyscrasias (anemia, thrombocytopenia, eosinophilia, leukopenia, agranulocytosis).International label, equivalent formulation · DailyMed (U.S. National Library of Medicine)

• History of a serious hypersensitivity reaction (e.g., anaphylaxis or Stevens-Johnson syndrome) to amoxicillin or to other beta-lactam antibacterial drugs (e.g., penicillins and cephalosporins).International label, equivalent formulation · DailyMed (U.S. National Library of Medicine)

• Serious and occasionally fatal anaphylactic reactions have been reported with penicillins; inquire about previous hypersensitivity to penicillins, cephalosporins or other allergens before starting; discontinue if an allergic reaction occurs.International label, equivalent formulation · DailyMed (U.S. National Library of Medicine)
• Severe cutaneous adverse reactions (SJS, TEN, DRESS, AGEP) and drug-induced enterocolitis syndrome (mostly in pediatric patients) may occur; discontinue if lesions progress or DIES occurs.International label, equivalent formulation · DailyMed (U.S. National Library of Medicine)
• Clostridioides difficile-associated diarrhea may occur (even more than 2 months after treatment); a high percentage of patients with mononucleosis develop erythematous rash - amoxicillin should not be given to patients with mononucleosis; prescribe only for proven or strongly suspected bacterial infection.International label, equivalent formulation · DailyMed (U.S. National Library of Medicine)

• ProbenecidDecreases renal tubular secretion of amoxicillin, resulting in increased and prolonged blood levels.DailyMed (U.S. National Library of Medicine)
• Oral anticoagulants (e.g., warfarin)Abnormal prolongation of prothrombin time (increased INR) has been reported; monitor and adjust the anticoagulant dose if necessary.DailyMed (U.S. National Library of Medicine)
• AllopurinolConcurrent use increases the incidence of rashes.DailyMed (U.S. National Library of Medicine)

• Reproduction studies in mice and rats at up to 2000 mg/kg showed no evidence of fetal harm; there are no adequate and well-controlled studies in pregnant women; use during pregnancy only if clearly needed.International label, equivalent formulation · DailyMed (U.S. National Library of Medicine)
• Penicillins are excreted in human milk; amoxicillin use by nursing mothers may lead to sensitization of infants - exercise caution.International label, equivalent formulation · DailyMed (U.S. National Library of Medicine)

• Amoxicillin: Bactericidal beta-lactam that inhibits bacterial cell-wall biosynthesis during active multiplication; inactivated by beta-lactamases (US label, section 12.4).