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|Erythromycin Ethylsuccinate/Sulfisoxazole |
Drugs search, click the first letter of a drug name: | A | B | C | D | E | F | G | H | I | J | K | L | M | N | O | P | Q | R | S | T | U | V | W | X | Y | Z | 1 | 2 | 3 | 4 | 5 | 6 | 8 | 9 Home Erythromycin Ethylsuccinate/SulfisoxazolePronouncation: (eh-RITH-row-MY-sin ETH-il-SUX-inate/sul-fih-SOX-uh-zole)Class: Antibiotic combination Trade Names: Trade Names: Mechanism of ActionPharmacologyErythromycin suppresses bacterial protein synthesis; sulfonamides interfere with bacterial folic acid synthesis. PharmacokineticsAbsorptionC max is 0.3 to 2 mcg/mL. T max is 1.6 hr. DistributionLargely bound to plasma proteins. Diffuses into most body fluids. Passage across the blood-brain barrier increases in meningitis. Crosses the placenta and is excreted in breast milk. MetabolismMetabolized in the liver by demethylation. EliminationMostly excreted in the bile; less than 5% recovered in the active form in the urine. Indications and UsageTreatment of acute otitis media in children caused by susceptible strains of Haemophilus influenzae . ContraindicationsHypersensitivity to chemically related drugs (eg, sulfonylureas, thiazide and loop diuretics, carbonic anhydrase inhibitors, sunscreens containing PABA, local anesthetics) or salicylates; patients taking terfenadine or astemizole; porphyria; use in infants younger than 20 mo, pregnant women at term and women nursing infants younger than 2 mo. Dosage and AdministrationChildrenPO 50 mg/kg/day erythromycin and 150 mg/kg/day (max 6 gm/day) sulfisoxazole in equally divided doses qid for 10 days. General Advice
Storage/StabilityRefrigerate after opening. Discard unused portion after 14 days. Drug InteractionsAnticoagulantsMay increase anticoagulant effects. Antihistamines, non-sedating (eg, astemizole, terfenadine)Erythromycin significantly alters metabolism of terfenadine. Rare cases of serious cardiovascular events including death have been reported. Astemizole, bromocriptine, carbamazepine, disopyramide, hexobarbital, methylprednisolone, phenytoinMay cause decreased metabolism and increased concentrations of these drugs. CyclosporineErythromycin may interfere with metabolism while sulfonamides may decrease cyclosporine levels; both increase risk of nephrotoxicity. DigoxinMay increase digoxin levels. LovastatinSevere myopathy or rhabdomyolysis may occur. MethotrexateSulfonamides can displace methotrexate from protein-binding sites and increase free methotrexate levels. SulfonylureasSulfisoxazole may potentiate hypoglycemic effects. TheophyllinesMay increase theophylline plasma concentrations. ThiopentalMay enhance anesthetic effects of thiopental. Laboratory Test InteractionsSulfosalicylic acid turbidity test for urinary proteinSulfisoxazole may produce false-positive results. Urinary glucose testSulfonamides may produce false-positive results when performed by Benedict"s method. Urobilistix testSulfisoxazole may interfere with test results. Adverse ReactionsCNSHeadache; peripheral neuropathy; dizziness; psychosis; hallucinations; depression; convulsions. DermatologicUrticaria; skin eruptions; pruritus; photosensitivity; anaphylaxis; erythema multiforme; toxic epidermal necrolysis; exfoliative dermatitis; angioedema; arteritis; vasculitis. EENTHearing loss (associated with high doses erythromycin and renal insufficiency). GINausea; vomiting; abdominal pain/cramping; diarrhea; anorexia. GenitourinaryCrystalluria; hematuria; increased BUN and creatinine; nephritis; toxic nephrosis with oliguria. HepaticHepatic dysfunction; abnormal LFT results; pseudomembranous colitis; GI hemorrhage; pancreatitis. HematologicLeukopenia; agranulocytosis; aplastic anemia; thrombocytopenia; hemolytic anemia; purpura; eosinophilia; clotting disorders; methemoglobinemia. MiscellaneousFever; chills; arthralgias; myalgias; periarteritis nodosum; systemic lupus erythematosus; serum sickness. Precautions
PregnancyCategory C . LactationBoth erythromycin and sulfisoxazole are excreted in breast milk. ChildrenDo not expose children younger than 2 mo (directly or through breast milk) to sulfonamides because of risk of kernicterus. Renal FunctionUse drug with caution in patients with renal or hepatic impairment. Hepatotoxicity has been associated with erythromycin. Hepatic FunctionUse drug with caution in patients with renal or hepatic impairment. Hepatotoxicity has been associated with erythromycin. Special Risk PatientsMay aggravate weakness in patients with myasthenia gravis. Use drug with caution in patients with severe allergies or bronchial asthma. Dose-related hemolytic anemia may occur in patients with G-6-PD deficiency. SuperinfectionProlonged use may result in bacterial or fungal overgrowth of nonsusceptible microorganisms. FatalitiesRare fatalities from severe reactions associated with hypersensitivity, agranulocytosis, aplastic anemia, blood dyscrasias, renal and hepatic damage, irreversible neuromuscular and CNS changes, and fibrosing alveolitis have been reported with sulfonamides. OtotoxicityMay occur, especially in patients with renal or hepatic insufficiency and elderly patients and with administration of large doses. Pseudomembranous colitisConsider possibility in patients with diarrhea. OverdosageSymptomsNausea, vomiting, diarrhea, hearing loss, vertigo, dizziness, headache, drowsiness, unconsciousness, toxic fever, acidosis, hemolytic anemia. Patient Information
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