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. 2018 Aug 15;2018(8):CD013099. doi: 10.1002/14651858.CD013099

Table 2.

Regimens and drug‐drug interactions of systemic antibiotics

Drug Dose/Regimen Drug‐Drug interaction (Gilbert 2018; Micromedex 2018)
Cefadroxil
  • Adult: 1 g orally daily in a single dose or in divided doses twice a day

  • Pediatric: 30 mg/kg orally once daily or in equally divided doses every 12 hours

  • Concurrent use of cefadroxil and warfarin may result in increased risk of bleeding

  • Concurrent use of cefadroxil and contraceptives (combination) may result in decreased contraceptive effectiveness

Ciprofloxacin
  • Adult: 500 mg orally every 12 hours for 7 to 14 days; 400 mg IV every 12 hours for 7 to 14 days

  • Concurrent use of ciprofloxacin and insulin and oral hypoglycaemics may result in increased or decreased blood sugar

  • Concurrent use of ciprofloxacin and caffeine may result in increased caffeine plasma concentrations

  • Concurrent use of ciprofloxacin and cimetidine may result in increased blood level of ciprofloxacin

  • Concurrent use of ciprofloxacin and cyclosporine may result in an increased cyclosporine plasma concentration

  • Concurrent use of ciprofloxacin and didanosine may result in a decreased ciprofloxacin plasma concentration

  • Concurrent use of ciprofloxacin and cations (e.g. Al3+, Ca2+, Fe2+, Mg2+, Zn2+) (cireate/citric acid) may result in a decreased plasma concentration of ciprofloxacin

  • Concurrent use of ciprofloxacin and methadone may result in an increased plasma concentration of methadone

  • Concurrent use of ciprofloxacin and NSAIDs may result in increased risk CNS stimulation/seizure

  • Concurrent use of ciprofloxacin and phenytoin may result in an increased or decreased plasma concentration of phenytoin

  • Concurrent use of ciprofloxacin and probenecid may result in a decreased plasma concentration of ciprofloxacin

  • Concurrent use of ciprofloxacin and rasagiline may result in an increased plasma concentration of rasagiline

  • Concurrent use of ciprofloxacin and sucralfate may result in decreased absorption of ciprofloxacin

  • Concurrent use of ciprofloxacin and theophylline may result in an increased plasma concentration of theophylline

  • Concurrent use of ciprofloxacin and thyroid hormone may result in a decreased plasma concentration of thyroid hormone

  • Concurrent use of ciprofloxacin and tizanidine may result in an increased plasma concentration of tizanidine

  • Concurrent use of ciprofloxacin and warfarin may result in increased prothrombin time

Clindamycin
  • Adult: 150 to 300 mg orally every 6 hours, 600 to 1200 mg/d IV or IM divided every 6 to 12 hours

  • Pediatric: 8 to 16 mg/kg/d ORALLY divided every 6 to 8 hours; 15 to 20 mg/kg/d IV or IM divided every 6 to 8 hours

  • Concurrent use of clindamycin and kaolin may result in decreased absorption of kaolin

  • Concurrent use of clindamycin and muscle relaxants (e.g. atracurium, baclofen, diazepam) may result in increased frequency and duration of respiratory paralysis

  • Concurrent use of clindamycin and St John’s wort may result in a decreased level of clindamycin

Tetracyclines
  • Adult: 500 mg orally twice daily or 250 mg orally 4 times per day

  • Pediatric: (older than 8 years) 25 to 50 mg/kg orally in 4 equally divided doses

  • Concurrent use of tetracycline and atovaquone may result in decreased atovaquone levels

  • Concurrent use of tetracycline and digoxin may result in increased toxicity of digoxin

  • Concurrent use of tetracycline and methoxyflurane may result in increased toxicity, polyuria, and renal failure

  • Concurrent use of tetracycline and sucralfate may result in decreased absorption of tetracycline

  • Concurrent use of tetracycline and aluminium, bismuth, iron, or Mg2+ may result in decreased absorption of tetracycline

  • Concurrent use of tetracycline and barbiturates or hydantoins may result in a decreased serum half‐life of tetracycline

  • Concurrent use of tetracycline and carbamazepine may result in a decreased serum half‐life of tetracycline

  • Concurrent use of tetracycline and digoxin may result in an increased serum level of digoxin

  • Concurrent use of tetracycline and warfarin may result in increased activity of warfarin

Trimethoprim‐sulphamethoxazole
  • Adult: sulfamethoxazole 800 mg/trimethoprim 160 mg to sulfamethoxazole 1600 mg/trimethoprim 320 mg orally twice daily

  • Pediatric: (older than 1 month) based on trimethoprim component: 8 to 12 mg/kg/d orally in 2 divided doses

  • Concurrent use of trimethoprim‐sulphamethoxazole and angiotensin‐converting enzyme inhibitors may result in an increased serum potassium concentration

  • Concurrent use of trimethoprim‐sulphamethoxazole and amantadine may result in increased serum levels and toxicity of tetracycline

  • Concurrent use of trimethoprim‐sulphamethoxazole and azathioprine may lead to side effects of leukopaenia

  • Concurrent use of trimethoprim‐sulphamethoxazole and barbiturates or hydantoins may result in a decreased serum half‐life of tetracycline

  • Concurrent use of trimethoprim‐sulphamethoxazole and loperamide may result in an increased serum level of loperamide

  • Concurrent use of trimethoprim‐sulphamethoxazole and methotrexate may result in enhanced marrow suppression

  • Concurrent use of trimethoprim‐sulphamethoxazole and oral contraceptives, pimozide, and 6‐mercaptopurine may result in decreased effects of oral contraceptives, pimozide, and 6‐mercaptopurine

  • Concurrent use of trimethoprim‐sulphamethoxazole and phenytoin may result in an increased serum level of phenytoin

  • Concurrent use of trimethoprim‐sulphamethoxazole and rifampin may result in an increased serum level of phenytoin

  • Concurrent use of trimethoprim‐sulphamethoxazole and spironolactone or sulfonylureas may result in an increased serum potassium level

  • Concurrent use of trimethoprim‐sulphamethoxazole and warfarin may result in increased activity of warfarin

Linezolid
  • Adult: 400 to 600 mg ORALLY every 12 hours for 10 to 14 days

  • Pediatric: (birth through 11 years) 10 mg/kg IV or ORALLY every 12 hours

  • Concurrent use of linezolid and adrenergic agents may result in increased risk of hypertension

  • Concurrent use of linezolid and clarithromycin may result in an increased blood concentration of linezolid

  • Concurrent use of linezolid and meperidine may result in increased risk of serotonin syndrome

  • Concurrent use of linezolid and rasagiline may result in increased risk of serotonin syndrome

  • Concurrent use of linezolid and rifampin may result in a decreased serum level of linezolid

  • Concurrent use of linezolid and serotonergic drugs may result in increased risk of serotonin syndrome

Glycopeptide (as vancomycin) Adult: 30 mg/kg/d IV in 2 divided doses or 40 mg/kg/d IV in 4 divided doses
  • Concurrent use of vancomycin and aminoglycosides may result in increased frequency of nephrotoxicity

Al: aluminium; Ca: calcium; CNS: central nervous system; Fe: iron; Mg: magnesium; NSAIDs: non‐steroidal anti‐inflammatory drugs; Zn: zinc.