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Indications ⬇

IM:

REMS


Unlabeled Use:
  • Inhaln: Treatment of PJP.

Contraind./Precautions ⬆ ⬇

Contraindicated in:

Use Cautiously in:

Adv. Reactions/Side Effects ⬆ ⬇

For parenteral form, unless otherwise indicated

EENT: inhalationburning in throat

Neuro: anxiety, headache, confusion, dizziness, hallucinations

Resp: inhalationbronchospasm, cough

CV: ARRHYTHMIAS, hypotension, chest pain

GI: PANCREATITIS, abdominal pain, anorexia, drug-induced hepatitis, nausea, unpleasant metallic taste, vomiting

GU: nephrotoxicity

Derm: pallor, rash

Endo: hypoglycemia, hyperglycemia

F and E: hyperkalemia, hypocalcemia

Hemat: anemia, leukopenia, thrombocytopenia

Local: IVphlebitis, pruritus, urticaria at IV site, IMsterile abscesses at IM sites

Misc: ANAPHYLAXISALLERGIC REACTIONS INCLUDING , STEVENS-JOHNSON SYNDROME, chills, fever

Interactions ⬆ ⬇

Interactions listed for parenteral administration

Availability ⬆ ⬇

(Generic available)

Route/Dosage ⬆ ⬇

Renal Impairment

US Brand Names ⬆ ⬇

NebuPent, Pentam 300

Action ⬆ ⬇

  • Appears to disrupt DNA or RNA synthesis.
  • Also has a direct toxic effect on pancreatic islet cells.
Therapeutic effects:
  • Death of susceptible organism.

Classifications ⬆ ⬇

Therapeutic Classification: anti-infectives

Pharmacokinetics ⬆ ⬇

Absorption: Well absorbed parenterally; Minimal systemic absorption occurs following inhalation.

Distribution: Widely and extensively distributed but does not cross the blood-brain barrier. Concentrates in liver, kidneys, lungs, and spleen, with prolonged storage in some tissues.

Metabolism/Excretion: 1–30% excreted unchanged by the kidneys. Remainder of metabolic fate unknown.

Half-Life: 5–11 hr (↑ in renal impairment).

Time/Action Profile ⬆ ⬇

(blood levels)

ROUTEONSETPEAKDURATION
IVunknownend of infusion24 hr
Inhalnunknownunknownunknown

Patient/Family Teaching ⬆ ⬇

Pronunciation ⬆ ⬇

pen-TAM-i-deen

Code ⬆

NDC Code