Medicine Overview

Indication

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Adult Dose

Clinical InformationAdministration Information
Indication: Metastatic breast cancer in postmenopausal women with oestrogen-receptor positive tumours
Age: Adult
Dose: Intramuscular – 500 mg (250 mg into each buttock)
Frequency: on days 1, 15, and 29, then once monthly thereafter
Indication: Metastatic breast cancer in postmenopausal women with oestrogen-receptor positive tumours
Age: Adult
Condition: Moderate (Child-Pugh Class B)
Dose: Intramuscular – 250 mg (into 1 buttock)
Frequency: on days 1, 15, and 29, then once monthly thereafter

Child Dose

Clinical InformationAdministration Information
Age: Child
Dose: No approved pediatric dosage available
Note: No approved pediatric dosage available

Renal Dose

Clinical InformationAdministration Information
Condition: Renal impairment
Dose: Injection – Negligible amounts
Note: Negligible amounts of fulvestrant are eliminated in urine. In clinical trials, fulvestrant concentrations in women with estimated creatinine clearance greater than or equal to 30 mL/minute were similar to women with normal creatinine.
Administration
  • Given as intramuscular injection
  • Must be administered by healthcare professionals
Side Effect

Drug Interaction

Drug NameRisk Factors
Anticoagulants (Warfarin, Heparin, Dabigatran, Rivaroxaban, Apixaban, Edoxaban)
Increased risk of bleeding when taken concomitantly

Disease Interaction

Disease NameRisk Factors
No specific contraindications listed
Monitor for general reactions

Pregnancy

Lactation
Special Use
Precaution
Overdose
Pharmacology
Storage

Details coming soon

Data Sources

Clinical & regulatory information on this page is compiled from the following government sources:

DISCLAIMER: This drug information content is provided for informational purposes only and is not intended to be a substitute for professional medical advice, diagnosis, or treatment. Patients should always consult their physician with any questions regarding a medical condition and to obtain medical advice and treatment.