section name header

Pronunciation

ful-VESS-trant

Classifications

Therapeutic Classification: antineoplastics

Pharmacologic Classification: estrogen receptor antagonists

Indications

REMS


Action

  • Competitively binds to estrogen receptors. Binding results in down-regulation of estrogen receptor protein in cancerous breast tissue.
Therapeutic effects:
  • Decreased progression of hormone receptor-positive breast cancer.

Pharmacokinetics

Absorption: Well absorbed following IM administration.

Distribution: Rapidly and extensively distributed.

Protein Binding: 99%.

Metabolism/Excretion: Mostly metabolized by the liver; negligible renal elimination.

Half-Life: 40 days.

Time/Action Profile

(effect on estrogen receptors)

ROUTEONSETPEAKDURATION
IMrapid7 days30 days



Contraind./Precautions

Contraindicated in:

Use Cautiously in:

Adv. Reactions/Side Effects

CV: vasodilation (hot flushes), chest pain, edema

Derm: rash, sweating

EENT: pharyngitis

GI: abdominal pain, constipation, diarrhea, nausea, vomiting, anorexia

GU: fertility, pelvic pain, urinary tract infection

Hemat: anemia

Local: pain/inflammation at injection site

MS: back pain, bone pain, arthritis

Neuro: headache, weakness, anxiety, depression, dizziness, injection site-related neurological events (including sciatica and neuropathy), insomnia, paresthesia

Resp: cough, dyspnea

Misc: fever, flu syndrome

Interactions

Drug-drug:

Route/Dosage

Monotherapy

Hepatic Impairment

In Combination with Palbociclib, Abemaciclib, or Ribociclib

Hepatic Impairment

Availability

(Generic available)

Assessment

Lab Test Considerations:

Implementation

Patient/Family Teaching

Evaluation/Desired Outcomes

US Brand Names

Faslodex

Code

NDC Code