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1 Contraindications/Precautions
Contraindicated in: Hypersensitivity to penicillins. PDF Page #1
ampicillin (am-pi-sil-in) Use Cautiously in: Severe renal insufficiency (doseprequired if CCr ⬍10 mL/
Classification min); Infectious mononucleosis, acute lymphocytic leukemia or cytomegalovirus in-
Therapeutic: anti-infectives fection (qincidence of rash); Patients allergic to cephalosporins; OB: Has been used
Pharmacologic: aminopenicillins during pregnancy; Lactation: Distributed into breast milk. Can cause rash, diar-
Pregnancy Category B rhea, and sensitization in the infant.
Adverse Reactions/Side Effects
Indications CNS: SEIZURES (high doses). GI: PSEUDOMEMBRANOUS COLITIS, diarrhea, nausea,
Treatment of the following infections: Skin and skin structure infections, Soft-tissue vomiting. Derm: rash, urticaria. Hemat: blood dyscrasias. Misc: allergic reac-
infections, Otitis media, Sinusitis, Respiratory infections, Genitourinary infections, tions including ANAPHYLAXIS and SERUM SICKNESS, superinfection.
Meningitis, Septicemia. Endocarditis prophylaxis. Unlabeled Use: Prevention of
infection in certain high-risk patients undergoing cesarean section. Interactions
Drug-Drug: Probenecidprenal excretion andqblood levels of ampicillin—
Action therapy may be combined for this purpose. Large doses mayqthe risk of bleeding
Binds to bacterial cell wall, resulting in cell death. Therapeutic Effects: Bacteri-
cidal action; spectrum is broader than penicillin. Spectrum: Active against: Strep- with warfarin.qrisk of with concurrent allopurinol therapy. Maypthe effective-
tococci, nonpenicillinase-producing staphylococci, Listeria, Pneumococci, Entero- ness of oral hormonal contraceptives.
cocci, Haemophilus influenzae, Escherichia coli, Enterobacter, Klebsiella, Route/Dosage
Proteus mirabilis, Neisseria meningitidis, N. gonorrhoeae, Shigella, Salmonella.
Respiratory and Soft-Tissue Infections
Pharmacokinetics PO (Adults and Children ⱖ20 kg): 250– 500 mg q 6 hr.
Absorption: Moderately absorbed from the duodenum (30– 50%). PO (Children ⬍20 kg): 50– 100 mg/kg/day in divided doses q 6– 8 hr (not to ex-
Distribution: Diffuses readily into body tissues and fluids. CSF penetration isqin ceed 2– 3 g/day).
the presence of inflamed meninges. Crosses the placenta; enters breast milk in small
amounts. IM, IV (Adults and Children ⱖ40 kg ): 500 mg to 3 g q 6 hr (not to exceed 14 g/
Metabolism and Excretion: Variably metabolized by the liver (12– 50%). Re- day).
nal excretion is variable (25– 60% after oral dosing; 50– 85% after IM administra- IM, IV (Children ⬍40 kg): 100– 200 mg/kg/day in divided doses q 6– 8 hr (not to
tion). exceed 12 g/day).
Half-life: Neonates: 1.7– 4 hr; Children and Adults: 1– 1.5 hr (qin renal impair- Bacterial Meningitis Caused by H. influenzae, Streptococcus pneu-
ment). moniae, Group B streptococcus or N. meningitidis or Septicemia
TIME/ACTION PROFILE (blood levels) IM, IV (Adults): 500 mg to 3 g q 6 hr (not to exceed 14 g/day).
ROUTE ONSET PEAK DURATION IM, IV (Children ⬎1 mo): 200– 400 mg/kg/day in divided doses q 6 hr (not to ex-
PO rapid 1.5–2 hr 4–6 hr ceed 12 g/day).
IM rapid 1 hr 4–6 hr IM, IV (Neonates ⱕ7 days): 200 mg/kg/day divided q 8 hr.
IV rapid end of infusion 4–6 hr IM, IV (Neonates ⬎7 days): 300 mg/kg/day divided q 6 hr.
⫽ Canadian drug name. ⫽ Genetic Implication. CAPITALS indicate life-threatening, underlines indicate most frequent. Strikethrough ⫽ Discontinued.
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