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FASLODEX- fulvestrant injection


  1. Patient Information
  2. Risk Of Bleeding:
  3. Embryo-fetal Toxicity:
  4. Lactation:

Patient Information 

Advise the patient to read the FDA-approved patient labeling (Patient Information).

Monotherapy

Risk Of Bleeding: 

Because FASLODEX is administered intramuscularly, it should be used with caution in patients with bleeding disorders, decreased platelet count, or in patients receiving anticoagulants (for example, warfarin)[seeWarnings and Precautions (5.1)].

Embryo-fetal Toxicity: 

Advise females of reproductive potential of the potential risk to a fetus and to use effective contraception during treatment with FASLODEX and for one year after the last dose. Advise females to inform their healthcare provider of a known or suspected pregnancy[seeWarnings and Precautions (5.4)andUse in Specific Populations (8.1),(8.3)].

Lactation: 

Advise women not to breastfeed during treatment with FASLODEX and for one year after the last dose[seeUse in Specific Populations (8.2)].

Combination Therapy

When FASLODEX is used in combination with palbociclib, abemaciclib, or ribociclib, refer to the respective Full Prescribing Information for Patient Counseling Information.



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