Other | Low Risk

Bortezomib (DBL Bortezomib)

What to know about Bortezomib — also sold as DBL Bortezomib, Bortezomib Juno, Bortezomib Ever Pharma, Bortezomib Accord, BORTRACZO and 4 more: uses, side effects, interactions, and safety considerations for people taking it or caring for someone who is.

Bortezomib (brand names: DBL Bortezomib, Bortezomib Juno, Bortezomib Ever Pharma, Bortezomib Accord, BORTRACZO and 4 more) is classified as Low risk (1 risk points) by AllMeds. It is a S4 medication under the TGA in Australia. FDA approved in the United States. Proteasome inhibitor chemotherapy agent with minimal impairment risk for work activities.

Key Takeaways

  • TGA Schedule: S4 in Australia
  • Risk level: Low (1 points)
  • PBS listed: Subsidised under the Australian Pharmaceutical Benefits Scheme

Scheduling and Classification

Jurisdiction Classification Status
Australia (TGA) S4 PBS listed
United States (FDA) Rx only FDA approved

Risk Profile

Risk Level Low
Risk Points 1
CNS Depressant No
Respiratory Risk No

Proteasome inhibitor chemotherapy agent with minimal impairment risk for work activities.

How Bortezomib is regulated

Bortezomib is overseen by medicines regulators in each country. The rules below explain how it's scheduled, what oversight applies, and what to discuss with your doctor or pharmacist before starting, changing, or stopping this medication.

Australia TGA / PBS / State Schemes

Classified as S4 under the Therapeutic Goods Administration (TGA).

Listed on the Pharmaceutical Benefits Scheme (PBS) for subsidised prescribing.

United States FDA / CDC / State WC

FDA approved for use in the United States.

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Important: This page is general health information, not personal medical advice. If you have questions about your medication — including starting it, stopping it, changing the dose, or combining it with something else — speak with your doctor or pharmacist. For an emergency or suspected overdose, call your local emergency number or poison information service immediately. Information is drawn from regulator and clinical guideline sources (TGA, FDA, MHRA, NICE, PBS, CDC); see our methodology for details.